| geneid | 10404 |
|---|---|
| ensemblid | ENSG00000104324.16 |
| hgncid | 16910 |
| symbol | CPQ |
| name | carboxypeptidase Q |
| refseq_nuc | NM_016134.4 |
| refseq_prot | NP_057218.1 |
| ensembl_nuc | ENST00000220763.10 |
| ensembl_prot | ENSP00000220763.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 96645242 |
| end | 97143501 |
| strand | + |
| ver | v1.2 |
| region | chr8:96645242-97143501 |
| region5000 | chr8:96640242-97148501 |
| regionname0 | CPQ_chr8_96645242_97143501 |
| regionname5000 | CPQ_chr8_96640242_97148501 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 472 | 109 | 41 | 19 | 34 | 5 | 8 | 30 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0002 | 0/0 | 472 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0003 | 0/0 | 472 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0004 | 0/0 | 472 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0005 | 0/0 | 472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0006 | 0/0 | 472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0007 | 0/0 | 472 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0008 | 0/0 | 472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0009 | 0/0 | 472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1419 | 55 | 19 | 12 | 17 | 3 | 4 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0002 | 1/1 | 1419 | 50 | 18 | 7 | 17 | 2 | 4 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0003 | 0/0 | 1419 | 8 | 8 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0004 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0005 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0006 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0007 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0008 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0009 | 0/0 | 1419 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0010 | 0/0 | 1419 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0011 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0012 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| c0013 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 514 | 104 | 43 | 14 | 32 | 6 | 7 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| t0002 | 0/0 | 513 | 20 | 13 | 6 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| t0003 | 0/0 | 514 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| t0004 | 0/0 | 514 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1419 | 55 | 19 | 12 | 17 | 3 | 4 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0002 | 1/1 | 1419 | 50 | 18 | 7 | 17 | 2 | 4 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0004 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0007 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0008 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0002c0003 | 0/0 | 1419 | 8 | 8 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0003c0005 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0004c0006 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0005c0013 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0006c0010 | 0/0 | 1419 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0007c0009 | 0/0 | 1419 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0008c0011 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0009c0012 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1932 | 41 | 10 | 8 | 16 | 3 | 4 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0001t0002 | 0/0 | 1931 | 13 | 9 | 4 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0001t0004 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0002t0001 | 1/1 | 1932 | 43 | 15 | 5 | 16 | 2 | 3 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0002t0002 | 0/0 | 1931 | 6 | 3 | 2 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0002t0003 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0004t0001 | 0/0 | 1932 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0007t0001 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0001c0008t0001 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0002c0003t0001 | 0/0 | 1932 | 8 | 8 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0003c0005t0001 | 0/0 | 1932 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0004c0006t0001 | 0/0 | 1932 | 2 | 2 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0005c0013t0001 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0006c0010t0001 | 0/0 | 1932 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0007c0009t0001 | 0/0 | 1932 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0008c0011t0002 | 0/0 | 1931 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| a0009c0012t0001 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | copy fasta | chr8 | 96640242 | 97148501 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0002t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0001c0008t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0003c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0003c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0004c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0004c0006t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0005c0013t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0006c0010t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0007c0009t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0008c0011t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| a0009c0012t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0007 | c0009 | t0001 | g0062 | EUR | GBR | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02004 | hp2 | a0006 | c0010 | t0001 | g0045 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0052 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02622 | hp1 | a0003 | c0005 | t0001 | g0068 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02647 | hp1 | a0001 | c0008 | t0001 | g0116 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0087 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02886 | hp2 | a0003 | c0005 | t0001 | g0007 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0054 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02965 | hp2 | a0009 | c0012 | t0001 | g0090 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0118 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03195 | hp1 | a0008 | c0011 | t0002 | g0037 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0053 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03225 | hp1 | a0004 | c0006 | t0001 | g0074 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03579 | hp1 | a0004 | c0006 | t0001 | g0075 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03579 | hp2 | a0001 | c0007 | t0001 | g0038 | AFR | MSL | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | BEB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18522 | hp1 | a0005 | c0013 | t0001 | g0043 | AFR | YRI | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0114 | AFR | YRI | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | CHB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19012 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0107 | AFR | LWK | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | LWK | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0089 | AFR | LWK | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | LWK | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | GIH | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | GIH | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | ACB | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | USA | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | USA | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0079 | REF | REF | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0126 | REF | REF | CPQ_chr8_96640242_97148501 | CPQ | chr8 | 96640242 | 97148501 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96784964
|
A | G | 1 | a0004 | 2 | HG03225.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.67A>G | p.Ile23Val | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/8 | 262/1932 | 67/1419 | 23/472 | chr8 | 96784964 | ||
| chr8:96784985
|
A | G | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.88A>G | p.Lys30Glu | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/8 | 283/1932 | 88/1419 | 30/472 | chr8 | 96784985 | ||
| chr8:96785003
|
A | G | 1 | a0009 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.106A>G | p.Ile36Val | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/8 | 301/1932 | 106/1419 | 36/472 | chr8 | 96785003 | ||
| chr8:96785310
|
G | A | 1 | a0002 | 8 | HG01884.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.413G>A | p.Ser138Asn | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/8 | 608/1932 | 413/1419 | 138/472 | chr8 | 96785310 | ||
| chr8:96835149
|
A | G | 1 | a0008 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.610A>G | p.Ile204Val | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/8 | 805/1932 | 610/1419 | 204/472 | chr8 | 96835149 | ||
| chr8:96880003
|
C | G | 1 | a0006 | 1 | HG02004.hp2 | missense_variant&splice_region_variant | MODERATE | c.847C>G | p.Gln283Glu | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/8 | 1042/1932 | 847/1419 | 283/472 | chr8 | 96880003 | ||
| chr8:97029409
|
G | A | 1 | a0007 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.968G>A | p.Arg323His | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/8 | 1163/1932 | 968/1419 | 323/472 | chr8 | 97029409 | ||
| chr8:97143025
|
A | G | 1 | a0003 | 2 | HG02622.hp1 HG02886.hp2 |
missense_variant | MODERATE | c.1261A>G | p.Ser421Gly | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 8/8 | 1456/1932 | 1261/1419 | 421/472 | chr8 | 97143025 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96785257
|
T | C | 1 | a0001c0007 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.360T>C | p.Ala120Ala | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/8 | 555/1932 | 360/1419 | 120/472 | chr8 | 96785257 | ||
| chr8:96835130
|
G | T | 4 | a0001c0001a0006c0010a0007c0009others(1): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
synonymous_variant | LOW | c.591G>T | p.Val197Val | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/8 | 786/1932 | 591/1419 | 197/472 | chr8 | 96835130 | ||
| chr8:96879831
|
C | T | 3 | a0001c0007a0001c0008a0008c0011 | 3 | HG02647.hp1 HG03195.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.675C>T | p.Gly225Gly | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/8 | 870/1932 | 675/1419 | 225/472 | chr8 | 96879831 | ||
| chr8:97029431
|
G | A | 1 | a0001c0004 | 2 | NA18522.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.990G>A | p.Leu330Leu | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/8 | 1185/1932 | 990/1419 | 330/472 | chr8 | 97029431 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96645272
|
G | C | 1 | a0001c0002t0003 | 1 | NA19012.hp1 | 5_prime_UTR_variant | MODIFIER | c.-165G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/8 | 139626 | chr8 | 96645272 | |||||
| chr8:97143214
|
CT | C | 3 | a0001c0001t0002a0001c0002t0002a0008c0011t0002 | 20 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*32delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 8/8 | 32 | chr8 | 97143214 | |||||
| chr8:97143452
|
T | C | 1 | a0001c0001t0004 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 8/8 | 269 | chr8 | 97143452 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:96645541
|
T | C | 1 | a0001c0002t0003g0001 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-35+139T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96645541 | ||||||
| chr8:96645666
|
G | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-35+264G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96645666 | ||||||
| chr8:96646074
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+672G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96646074 | ||||||
| chr8:96646126
|
G | C | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-35+724G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96646126 | ||||||
| chr8:96646978
|
C | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-35+1576C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96646978 | ||||||
| chr8:96647045
|
T | C | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+1643T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96647045 | ||||||
| chr8:96647070
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(24): Show | 27 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.-35+1668G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96647070 | ||||||
| chr8:96647140
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+1738C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96647140 | ||||||
| chr8:96647180
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-35+1778G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96647180 | ||||||
| chr8:96647430
|
A | G | 46 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(43): Show | 46 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-35+2028A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96647430 | ||||||
| chr8:96647918
|
AAGCAGTG others(14): Show |
A | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-35+2520_-35+2540d others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96647918 | |||||
| chr8:96647975
|
CT | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+2574delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96647975 | ||||||
| chr8:96648043
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG01081.hp1 HG01516.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+2641A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96648043 | ||||||
| chr8:96648209
|
AAG | A | 3 | a0001c0002t0001g0088a0002c0003t0001g0087a0002c0003t0001g0089 | 3 | HG02809.hp1 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-35+2810_-35+2811d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96648209 | |||||
| chr8:96649069
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+3667C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96649069 | ||||||
| chr8:96649186
|
A | G | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-35+3784A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96649186 | ||||||
| chr8:96649261
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-35+3859G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96649261 | ||||||
| chr8:96649736
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+4334A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96649736 | ||||||
| chr8:96649840
|
A | C | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-35+4438A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96649840 | ||||||
| chr8:96650040
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+4638A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96650040 | ||||||
| chr8:96650135
|
G | C | 49 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(46): Show | 49 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.-35+4733G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96650135 | ||||||
| chr8:96650535
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-35+5133C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96650535 | ||||||
| chr8:96650827
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(14): Show | 17 | HG01884.hp1 HG02004.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-35+5425G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96650827 | ||||||
| chr8:96650886
|
T | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(23): Show | 26 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+5484T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96650886 | ||||||
| chr8:96651036
|
T | C | 58 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0042others(55): Show | 58 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-35+5634T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96651036 | ||||||
| chr8:96651088
|
G | T | 45 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(42): Show | 45 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-35+5686G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96651088 | ||||||
| chr8:96651497
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-35+6095G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96651497 | ||||||
| chr8:96651532
|
T | A | 125 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(122): Show |
intron_variant | MODIFIER | c.-35+6130T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96651532 | ||||||
| chr8:96651694
|
A | C | 28 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(25): Show | 28 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+6292A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96651694 | ||||||
| chr8:96651700
|
ATATTT | A | 46 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(43): Show | 46 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-35+6303_-35+6307d others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96651700 | |||||
| chr8:96651892
|
G | A | 49 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(46): Show | 49 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.-35+6490G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96651892 | ||||||
| chr8:96652053
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+6651G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652053 | ||||||
| chr8:96652054
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+6652C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652054 | ||||||
| chr8:96652106
|
A | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(27): Show | 30 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.-35+6704A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652106 | ||||||
| chr8:96652192
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+6790T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652192 | ||||||
| chr8:96652344
|
A | G | 46 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(43): Show | 46 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-35+6942A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652344 | ||||||
| chr8:96652440
|
T | C | 4 | a0001c0002t0001g0040a0001c0002t0002g0039a0001c0007t0001g0038others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+7038T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652440 | ||||||
| chr8:96652639
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+7237T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652639 | ||||||
| chr8:96652714
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+7312G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652714 | ||||||
| chr8:96652719
|
G | A | 2 | a0001c0001t0002g0044a0005c0013t0001g0043 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-35+7317G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652719 | ||||||
| chr8:96652792
|
C | T | 2 | a0001c0001t0002g0044a0005c0013t0001g0043 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-35+7390C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652792 | ||||||
| chr8:96652900
|
C | A | 4 | a0001c0002t0001g0095a0001c0002t0001g0096a0001c0002t0001g0097others(1): Show | 4 | NA18990.hp1 NA19012.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+7498C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96652900 | ||||||
| chr8:96653411
|
G | A | 4 | a0001c0002t0001g0040a0001c0002t0002g0039a0001c0007t0001g0038others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+8009G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96653411 | ||||||
| chr8:96653794
|
A | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+8392A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96653794 | ||||||
| chr8:96653890
|
G | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(19): Show | 22 | HG01081.hp1 HG01516.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35+8488G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96653890 | ||||||
| chr8:96654049
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+8647T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96654049 | ||||||
| chr8:96654424
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-35+9022A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96654424 | ||||||
| chr8:96654425
|
T | C | 1 | a0001c0002t0002g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-35+9023T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96654425 | ||||||
| chr8:96654954
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+9552T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96654954 | ||||||
| chr8:96655103
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+9701T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655103 | ||||||
| chr8:96655156
|
A | G | 2 | a0001c0002t0001g0081a0001c0002t0002g0082 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-35+9754A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655156 | ||||||
| chr8:96655162
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0002g0099a0001c0001t0002g0100others(2): Show | 5 | HG01975.hp2 HG01981.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+9760T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655162 | ||||||
| chr8:96655364
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+9962T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655364 | ||||||
| chr8:96655484
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+10082A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655484 | ||||||
| chr8:96655707
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+10305T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655707 | ||||||
| chr8:96655726
|
G | T | 1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-35+10324G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655726 | ||||||
| chr8:96655793
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(84): Show | 87 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-35+10391G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96655793 | ||||||
| chr8:96656182
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+10780G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96656182 | ||||||
| chr8:96656329
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+10927G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96656329 | ||||||
| chr8:96656380
|
T | C | 1 | a0001c0001t0002g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-35+10978T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96656380 | ||||||
| chr8:96656514
|
GC | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0080 | 2 | NA19012.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-35+11113delC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96656514 | ||||||
| chr8:96656614
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+11212G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96656614 | ||||||
| chr8:96656822
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+11420T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96656822 | ||||||
| chr8:96657019
|
C | CT | 6 | a0001c0001t0001g0035a0001c0001t0002g0099a0001c0002t0001g0005others(3): Show | 6 | HG01516.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+11631dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96657019 | |||||
| chr8:96657329
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+11927A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96657329 | ||||||
| chr8:96658042
|
A | G | 2 | a0001c0002t0002g0039a0001c0007t0001g0038 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-35+12640A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658042 | ||||||
| chr8:96658180
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+12778C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658180 | ||||||
| chr8:96658489
|
TCCCTACC others(3): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-35+13094_-35+1310 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96658489 | |||||
| chr8:96658667
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+13265A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658667 | ||||||
| chr8:96658671
|
G | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+13269G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658671 | ||||||
| chr8:96658730
|
A | G | 2 | a0004c0006t0001g0074a0004c0006t0001g0075 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-35+13328A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658730 | ||||||
| chr8:96658768
|
G | A | 42 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(39): Show | 42 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-35+13366G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658768 | ||||||
| chr8:96658859
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+13457C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96658859 | ||||||
| chr8:96659155
|
G | T | 5 | a0001c0001t0001g0102a0001c0001t0002g0099a0001c0001t0002g0100others(2): Show | 5 | HG01975.hp2 HG01981.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+13753G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96659155 | ||||||
| chr8:96659185
|
G | GTGGT | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+13785_-35+1378 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96659185 | |||||
| chr8:96659276
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+13874C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96659276 | ||||||
| chr8:96659669
|
G | A | 73 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(70): Show | 73 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.-35+14267G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96659669 | ||||||
| chr8:96659932
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+14530G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96659932 | ||||||
| chr8:96660295
|
CCT | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+14894_-35+1489 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96660295 | ||||||
| chr8:96660636
|
G | GGT | 33 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0047others(30): Show | 33 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-35+15261_-35+1526 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96660636 | |||||
| chr8:96660636
|
G | GGTGT | 46 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0057others(43): Show | 46 | HG01261.hp1 HG01261.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.-35+15259_-35+1526 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96660636 | |||||
| chr8:96660636
|
G | GGTGTGT | 8 | a0001c0001t0001g0105a0001c0002t0001g0005a0001c0002t0001g0006others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+15257_-35+1526 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96660636 | |||||
| chr8:96660636
|
GGT | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(7): Show | 10 | HG00733.hp2 HG01255.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+15261_-35+1526 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96660636 | |||||
| chr8:96660659
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+15257G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96660659 | ||||||
| chr8:96660821
|
C | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(83): Show | 86 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.-35+15419C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96660821 | ||||||
| chr8:96660925
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15523A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96660925 | ||||||
| chr8:96661243
|
A | C | 1 | a0001c0002t0002g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-35+15841A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96661243 | ||||||
| chr8:96661258
|
C | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+15856C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96661258 | ||||||
| chr8:96661311
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+15909G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96661311 | ||||||
| chr8:96661484
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+16082C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96661484 | ||||||
| chr8:96661493
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-35+16091C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96661493 | ||||||
| chr8:96661757
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+16355G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96661757 | ||||||
| chr8:96662010
|
C | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0003c0005t0001g0007 | 3 | HG02280.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-35+16608C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662010 | ||||||
| chr8:96662162
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+16760C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662162 | ||||||
| chr8:96662183
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-35+16781G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662183 | ||||||
| chr8:96662374
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+16972A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662374 | ||||||
| chr8:96662537
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+17135T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662537 | ||||||
| chr8:96662608
|
C | A | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+17206C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662608 | ||||||
| chr8:96662777
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-35+17375C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662777 | ||||||
| chr8:96662867
|
G | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(82): Show | 85 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.-35+17465G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96662867 | ||||||
| chr8:96663319
|
T | TACATGAC | 76 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(73): Show | 76 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.-35+17919_-35+1792 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96663319 | |||||
| chr8:96663351
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-35+17949A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96663351 | ||||||
| chr8:96663805
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-35+18403A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96663805 | ||||||
| chr8:96663863
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+18461A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96663863 | ||||||
| chr8:96663944
|
T | C | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-35+18542T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96663944 | ||||||
| chr8:96664765
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-35+19363G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96664765 | ||||||
| chr8:96664854
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(84): Show | 87 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-35+19452G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96664854 | ||||||
| chr8:96665065
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-35+19663G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96665065 | ||||||
| chr8:96665512
|
T | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+20110T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96665512 | ||||||
| chr8:96665515
|
C | T | 1 | a0001c0002t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-35+20113C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96665515 | ||||||
| chr8:96665634
|
G | C | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35+20232G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96665634 | ||||||
| chr8:96666216
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-35+20814T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96666216 | ||||||
| chr8:96666428
|
C | T | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(74): Show | 77 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.-35+21026C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96666428 | ||||||
| chr8:96666439
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+21037A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96666439 | ||||||
| chr8:96667101
|
C | CA | 71 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(68): Show | 71 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.-35+21706dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96667101 | |||||
| chr8:96667112
|
A | AC | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+21714dupC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96667112 | |||||
| chr8:96667159
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+21757C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667159 | ||||||
| chr8:96667186
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+21784T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667186 | ||||||
| chr8:96667276
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+21874C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667276 | ||||||
| chr8:96667277
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+21875A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667277 | ||||||
| chr8:96667351
|
C | CT | 5 | a0001c0001t0001g0057a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+21966dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96667351 | |||||
| chr8:96667351
|
CT | C | 4 | a0001c0001t0001g0077a0001c0001t0002g0011a0001c0002t0001g0059others(1): Show | 4 | HG01975.hp1 HG02004.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+21966delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96667351 | |||||
| chr8:96667391
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(85): Show | 88 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+21989T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667391 | ||||||
| chr8:96667446
|
T | C | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-35+22044T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667446 | ||||||
| chr8:96667505
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-35+22103C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667505 | ||||||
| chr8:96667535
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0080 | 2 | NA19012.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-35+22133G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667535 | ||||||
| chr8:96667617
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+22215A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667617 | ||||||
| chr8:96667638
|
C | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+22236C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667638 | ||||||
| chr8:96667646
|
G | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+22244G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667646 | ||||||
| chr8:96667701
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+22299T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96667701 | ||||||
| chr8:96668005
|
A | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+22603A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668005 | ||||||
| chr8:96668442
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+23040A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668442 | ||||||
| chr8:96668469
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+23067A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668469 | ||||||
| chr8:96668498
|
A | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+23096A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668498 | ||||||
| chr8:96668526
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+23124G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668526 | ||||||
| chr8:96668580
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-35+23178A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668580 | ||||||
| chr8:96668590
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+23188G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668590 | ||||||
| chr8:96668669
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+23267G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668669 | ||||||
| chr8:96668871
|
C | CA | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+23481dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96668871 | |||||
| chr8:96668941
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+23539A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96668941 | ||||||
| chr8:96669983
|
A | G | 42 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(39): Show | 42 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-35+24581A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96669983 | ||||||
| chr8:96670256
|
G | A | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+24854G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96670256 | ||||||
| chr8:96670310
|
A | AT | 5 | a0001c0001t0001g0014a0001c0001t0001g0080a0001c0001t0002g0011others(2): Show | 5 | HG02809.hp2 HG02895.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+24935dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96670310 | |||||
| chr8:96670310
|
A | ATTTTTTT others(3): Show |
1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+24926_-35+2493 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96670310 | |||||
| chr8:96670310
|
AT | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0033others(1): Show | 4 | HG02922.hp1 HG02965.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+24935delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96670310 | |||||
| chr8:96670310
|
ATTT | A | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+24933_-35+2493 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96670310 | |||||
| chr8:96670319
|
T | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+24917T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96670319 | ||||||
| chr8:96670323
|
T | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+24921T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96670323 | ||||||
| chr8:96670327
|
T | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+24925T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96670327 | ||||||
| chr8:96670337
|
TG | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+24937delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96670337 | |||||
| chr8:96670338
|
G | T | 72 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(69): Show | 72 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35+24936G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96670338 | ||||||
| chr8:96670356
|
C | T | 2 | a0001c0002t0001g0069a0003c0005t0001g0068 | 2 | HG01081.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-35+24954C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96670356 | ||||||
| chr8:96670924
|
AGGAC | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+25530_-35+2553 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96670924 | |||||
| chr8:96671117
|
T | G | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-35+25715T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96671117 | ||||||
| chr8:96671241
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+25839C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96671241 | ||||||
| chr8:96671320
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-35+25918G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96671320 | ||||||
| chr8:96671461
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+26059C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96671461 | ||||||
| chr8:96671475
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0125 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-35+26073C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96671475 | ||||||
| chr8:96671932
|
G | T | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+26530G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96671932 | ||||||
| chr8:96672054
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-35+26652C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672054 | ||||||
| chr8:96672097
|
CTA | C | 67 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(64): Show | 67 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35+26697_-35+2669 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96672097 | |||||
| chr8:96672115
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-35+26713G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672115 | ||||||
| chr8:96672136
|
G | A | 21 | a0001c0001t0001g0036a0001c0001t0001g0108a0001c0001t0001g0110others(18): Show | 21 | HG02040.hp2 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-35+26734G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672136 | ||||||
| chr8:96672146
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+26744C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672146 | ||||||
| chr8:96672453
|
A | T | 2 | a0001c0002t0001g0120a0001c0002t0001g0121 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-35+27051A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672453 | ||||||
| chr8:96672842
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+27440T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672842 | ||||||
| chr8:96672868
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-35+27466G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672868 | ||||||
| chr8:96672870
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+27468G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672870 | ||||||
| chr8:96672983
|
C | A | 70 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(67): Show | 70 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.-35+27581C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96672983 | ||||||
| chr8:96673120
|
A | C | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+27718A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673120 | ||||||
| chr8:96673200
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+27798C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673200 | ||||||
| chr8:96673362
|
G | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+27960G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673362 | ||||||
| chr8:96673363
|
C | A | 26 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(23): Show | 26 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+27961C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673363 | ||||||
| chr8:96673530
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+28128T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673530 | ||||||
| chr8:96673602
|
G | A | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+28200G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673602 | ||||||
| chr8:96673735
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-35+28333G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673735 | ||||||
| chr8:96673911
|
TAGAAAAG | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-35+28515_-35+2852 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96673911 | |||||
| chr8:96673941
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-35+28539C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673941 | ||||||
| chr8:96673987
|
G | GT | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.-35+28585_-35+2858 others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96673987 | ||||||
| chr8:96674112
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+28710A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96674112 | ||||||
| chr8:96674335
|
C | T | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+28933C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96674335 | ||||||
| chr8:96674339
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+28937C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96674339 | ||||||
| chr8:96674639
|
A | G | 2 | a0004c0006t0001g0074a0004c0006t0001g0075 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-35+29237A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96674639 | ||||||
| chr8:96674782
|
CA | C | 2 | a0001c0002t0001g0088a0002c0003t0001g0089 | 2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-35+29381delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96674782 | ||||||
| chr8:96675081
|
G | T | 67 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(64): Show | 67 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35+29679G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675081 | ||||||
| chr8:96675255
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+29853G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675255 | ||||||
| chr8:96675509
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+30107A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675509 | ||||||
| chr8:96675537
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+30135G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675537 | ||||||
| chr8:96675648
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30246G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675648 | ||||||
| chr8:96675673
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-35+30271C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675673 | ||||||
| chr8:96675723
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30321G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675723 | ||||||
| chr8:96675756
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+30354G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675756 | ||||||
| chr8:96675829
|
T | A | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-35+30427T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675829 | ||||||
| chr8:96675952
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30550A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96675952 | ||||||
| chr8:96676189
|
C | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30787C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676189 | ||||||
| chr8:96676196
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30794G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676196 | ||||||
| chr8:96676252
|
T | A | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-35+30850T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676252 | ||||||
| chr8:96676253
|
C | T | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-35+30851C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676253 | ||||||
| chr8:96676351
|
A | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+30949A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676351 | ||||||
| chr8:96676354
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+30952G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676354 | ||||||
| chr8:96676377
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30975A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676377 | ||||||
| chr8:96676463
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+31061T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676463 | ||||||
| chr8:96676609
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103 | 3 | HG01975.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-35+31207A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676609 | ||||||
| chr8:96676908
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+31506T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96676908 | ||||||
| chr8:96677041
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+31639G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677041 | ||||||
| chr8:96677062
|
TTTAC | T | 2 | a0001c0002t0001g0088a0002c0003t0001g0089 | 2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-35+31663_-35+3166 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96677062 | |||||
| chr8:96677159
|
C | CA | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+31757_-35+3175 others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677159 | ||||||
| chr8:96677160
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+31758G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677160 | ||||||
| chr8:96677392
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+31990T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677392 | ||||||
| chr8:96677443
|
G | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32041G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677443 | ||||||
| chr8:96677447
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32045G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677447 | ||||||
| chr8:96677489
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-35+32087A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677489 | ||||||
| chr8:96677495
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32093C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677495 | ||||||
| chr8:96677550
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-35+32148C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96677550 | ||||||
| chr8:96678021
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32619G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678021 | ||||||
| chr8:96678270
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32868C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678270 | ||||||
| chr8:96678356
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32954T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678356 | ||||||
| chr8:96678427
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-35+33025C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678427 | ||||||
| chr8:96678435
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+33033A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678435 | ||||||
| chr8:96678526
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+33124C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678526 | ||||||
| chr8:96678591
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+33189C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678591 | ||||||
| chr8:96678600
|
A | G | 2 | a0001c0002t0001g0081a0001c0002t0002g0082 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-35+33198A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678600 | ||||||
| chr8:96678758
|
C | CT | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(38): Show | 41 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.-35+33372dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96678758 | |||||
| chr8:96678758
|
C | CTT | 4 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0002t0001g0084others(1): Show | 4 | HG01255.hp2 HG02004.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+33371_-35+3337 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96678758 | |||||
| chr8:96678758
|
C | CTTT | 69 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(66): Show | 69 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.-35+33370_-35+3337 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96678758 | |||||
| chr8:96678758
|
C | CTTTT | 4 | a0001c0001t0001g0108a0001c0002t0001g0088a0001c0002t0003g0001others(1): Show | 4 | HG02040.hp2 HG02895.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+33369_-35+3337 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96678758 | |||||
| chr8:96678758
|
CT | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+33372delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96678758 | |||||
| chr8:96678923
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+33521G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678923 | ||||||
| chr8:96678931
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+33529G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96678931 | ||||||
| chr8:96679185
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0024others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+33783G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679185 | ||||||
| chr8:96679186
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+33784G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679186 | ||||||
| chr8:96679312
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+33910G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679312 | ||||||
| chr8:96679503
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34101G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679503 | ||||||
| chr8:96679641
|
T | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(85): Show | 88 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+34239T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679641 | ||||||
| chr8:96679699
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34297A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679699 | ||||||
| chr8:96679755
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34353C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96679755 | ||||||
| chr8:96679764
|
C | CT | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0119others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+34373dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96679764 | |||||
| chr8:96679957
|
T | TA | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34556dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96679957 | |||||
| chr8:96680037
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34635T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680037 | ||||||
| chr8:96680070
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34668C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680070 | ||||||
| chr8:96680093
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34691G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680093 | ||||||
| chr8:96680094
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+34692A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680094 | ||||||
| chr8:96680263
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+34861C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680263 | ||||||
| chr8:96680343
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+34941G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680343 | ||||||
| chr8:96680347
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+34945T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680347 | ||||||
| chr8:96680381
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+34979T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680381 | ||||||
| chr8:96680397
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+34995C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680397 | ||||||
| chr8:96680529
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+35127C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680529 | ||||||
| chr8:96680569
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+35167A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96680569 | ||||||
| chr8:96681277
|
G | A | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+35875G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681277 | ||||||
| chr8:96681412
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+36010C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681412 | ||||||
| chr8:96681525
|
G | A | 72 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(69): Show | 72 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35+36123G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681525 | ||||||
| chr8:96681527
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+36125A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681527 | ||||||
| chr8:96681562
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.-35+36160T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681562 | ||||||
| chr8:96681578
|
T | C | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+36176T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681578 | ||||||
| chr8:96681614
|
C | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+36212C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681614 | ||||||
| chr8:96681850
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+36448G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96681850 | ||||||
| chr8:96682010
|
T | A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-35+36608T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682010 | ||||||
| chr8:96682130
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+36728G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682130 | ||||||
| chr8:96682169
|
G | C | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+36767G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682169 | ||||||
| chr8:96682185
|
T | C | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+36783T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682185 | ||||||
| chr8:96682235
|
G | A | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+36833G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682235 | ||||||
| chr8:96682264
|
C | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.-35+36862C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682264 | ||||||
| chr8:96682348
|
A | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+36946A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682348 | ||||||
| chr8:96682455
|
C | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-35+37053C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682455 | ||||||
| chr8:96682498
|
T | C | 1 | a0001c0002t0001g0081 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-35+37096T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682498 | ||||||
| chr8:96682524
|
C | A | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+37122C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682524 | ||||||
| chr8:96682636
|
T | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(76): Show | 79 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+37234T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682636 | ||||||
| chr8:96682978
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+37576C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96682978 | ||||||
| chr8:96683042
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+37640A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96683042 | ||||||
| chr8:96683090
|
G | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+37688G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96683090 | ||||||
| chr8:96683138
|
G | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+37736G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96683138 | ||||||
| chr8:96683766
|
TA | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(8): Show | 11 | HG00733.hp2 HG01255.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35+38376delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96683766 | |||||
| chr8:96683766
|
TAA | T | 76 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0046others(73): Show | 76 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.-35+38375_-35+3837 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96683766 | |||||
| chr8:96683805
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+38403T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96683805 | ||||||
| chr8:96683808
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+38406G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96683808 | ||||||
| chr8:96684169
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+38767G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684169 | ||||||
| chr8:96684209
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+38807G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684209 | ||||||
| chr8:96684226
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+38824T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684226 | ||||||
| chr8:96684484
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39082G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684484 | ||||||
| chr8:96684487
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39085C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684487 | ||||||
| chr8:96684488
|
G | A | 12 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(9): Show | 12 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-35+39086G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684488 | ||||||
| chr8:96684557
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39155C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684557 | ||||||
| chr8:96684649
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-35+39247A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684649 | ||||||
| chr8:96684664
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39262G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684664 | ||||||
| chr8:96684747
|
G | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+39345G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684747 | ||||||
| chr8:96684771
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-35+39369C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684771 | ||||||
| chr8:96684827
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39425T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684827 | ||||||
| chr8:96684901
|
C | T | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-35+39499C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684901 | ||||||
| chr8:96684924
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39522T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684924 | ||||||
| chr8:96684935
|
TA | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+39544delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96684935 | |||||
| chr8:96684973
|
G | A | 1 | a0001c0002t0001g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-35+39571G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96684973 | ||||||
| chr8:96685059
|
G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0060 | 2 | HG01261.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-35+39657G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685059 | ||||||
| chr8:96685128
|
A | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+39726A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685128 | ||||||
| chr8:96685136
|
C | CAACAAAA others(12): Show |
78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+39736_-35+3973 others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96685136 | |||||
| chr8:96685283
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+39881T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685283 | ||||||
| chr8:96685441
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40039G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685441 | ||||||
| chr8:96685454
|
G | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40052G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685454 | ||||||
| chr8:96685455
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40053G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685455 | ||||||
| chr8:96685519
|
G | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40117G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685519 | ||||||
| chr8:96685581
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0020others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+40179T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685581 | ||||||
| chr8:96685636
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40234C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685636 | ||||||
| chr8:96685801
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+40399T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685801 | ||||||
| chr8:96685878
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40476G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96685878 | ||||||
| chr8:96686014
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40612G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686014 | ||||||
| chr8:96686020
|
T | C | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+40618T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686020 | ||||||
| chr8:96686174
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40772C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686174 | ||||||
| chr8:96686178
|
A | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40776A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686178 | ||||||
| chr8:96686297
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-35+40895T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686297 | ||||||
| chr8:96686378
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+40976G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686378 | ||||||
| chr8:96686397
|
A | G | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+40995A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686397 | ||||||
| chr8:96686596
|
G | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+41194G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686596 | ||||||
| chr8:96686597
|
C | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+41195C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686597 | ||||||
| chr8:96686865
|
A | C | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-35+41463A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686865 | ||||||
| chr8:96686876
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+41474T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686876 | ||||||
| chr8:96686910
|
C | T | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+41508C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686910 | ||||||
| chr8:96686933
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+41531A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96686933 | ||||||
| chr8:96687062
|
T | C | 73 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(70): Show | 73 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.-35+41660T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687062 | ||||||
| chr8:96687086
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+41684G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687086 | ||||||
| chr8:96687149
|
TTTTTC | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+41771_-35+4177 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96687149 | |||||
| chr8:96687175
|
TTTCTC | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0117 | 2 | HG01255.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-35+41793_-35+4179 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96687175 | |||||
| chr8:96687180
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+41778C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687180 | ||||||
| chr8:96687290
|
G | A | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+41888G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687290 | ||||||
| chr8:96687357
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+41955C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687357 | ||||||
| chr8:96687367
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+41965C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687367 | ||||||
| chr8:96687401
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+41999T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687401 | ||||||
| chr8:96687432
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(75): Show | 78 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+42030C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687432 | ||||||
| chr8:96687587
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+42185T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687587 | ||||||
| chr8:96687603
|
G | A | 41 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(38): Show | 41 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.-35+42201G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687603 | ||||||
| chr8:96687649
|
G | A | 2 | a0001c0002t0002g0039a0001c0007t0001g0038 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-35+42247G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687649 | ||||||
| chr8:96687848
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+42446T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687848 | ||||||
| chr8:96687867
|
A | C | 2 | a0004c0006t0001g0074a0004c0006t0001g0075 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-35+42465A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687867 | ||||||
| chr8:96687867
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+42465A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687867 | ||||||
| chr8:96687892
|
G | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+42490G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96687892 | ||||||
| chr8:96688008
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+42606T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96688008 | ||||||
| chr8:96688133
|
TTAGA | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+42735_-35+4273 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96688133 | |||||
| chr8:96688388
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+42986C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96688388 | ||||||
| chr8:96688478
|
C | T | 2 | a0001c0002t0002g0039a0001c0007t0001g0038 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-35+43076C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96688478 | ||||||
| chr8:96688518
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-35+43116G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96688518 | ||||||
| chr8:96688569
|
TTTATAA | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+43173_-35+4317 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96688569 | |||||
| chr8:96689019
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+43617A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689019 | ||||||
| chr8:96689141
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+43739C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689141 | ||||||
| chr8:96689212
|
C | G | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-35+43810C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689212 | ||||||
| chr8:96689336
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+43934C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689336 | ||||||
| chr8:96689438
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+44036G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689438 | ||||||
| chr8:96689441
|
A | C | 73 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0001t0001g0047others(70): Show | 73 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.-35+44039A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689441 | ||||||
| chr8:96689496
|
T | C | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-35+44094T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689496 | ||||||
| chr8:96689678
|
G | GA | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+44281dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96689678 | |||||
| chr8:96689749
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+44347A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689749 | ||||||
| chr8:96689793
|
C | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+44391C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689793 | ||||||
| chr8:96689891
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.-35+44489T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689891 | ||||||
| chr8:96689987
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-35+44585C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96689987 | ||||||
| chr8:96690372
|
A | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+44970A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96690372 | ||||||
| chr8:96690391
|
T | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(85): Show | 88 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+44989T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96690391 | ||||||
| chr8:96690546
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-35+45144A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96690546 | ||||||
| chr8:96690661
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-35+45259C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96690661 | ||||||
| chr8:96690721
|
A | G | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+45319A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96690721 | ||||||
| chr8:96690829
|
AGGGCCAC others(5): Show |
A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+45430_-35+4544 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96690829 | |||||
| chr8:96691006
|
T | TCATGTAA others(45): Show |
6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+45604_-35+4560 others(56): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691006 | ||||||
| chr8:96691028
|
A | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(83): Show | 86 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.-35+45626A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691028 | ||||||
| chr8:96691143
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+45741T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691143 | ||||||
| chr8:96691255
|
C | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+45853C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691255 | ||||||
| chr8:96691528
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+46126A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691528 | ||||||
| chr8:96691708
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+46306C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691708 | ||||||
| chr8:96691777
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-35+46375G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691777 | ||||||
| chr8:96691891
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+46489C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691891 | ||||||
| chr8:96691965
|
C | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+46563C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691965 | ||||||
| chr8:96691992
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+46590C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691992 | ||||||
| chr8:96691997
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+46595A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96691997 | ||||||
| chr8:96692056
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+46654T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692056 | ||||||
| chr8:96692306
|
A | G | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+46904A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692306 | ||||||
| chr8:96692367
|
A | G | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.-35+46965A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692367 | ||||||
| chr8:96692437
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+47035G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692437 | ||||||
| chr8:96692560
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+47158G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692560 | ||||||
| chr8:96692584
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+47182C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692584 | ||||||
| chr8:96692595
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-35+47193C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692595 | ||||||
| chr8:96692613
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+47211A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692613 | ||||||
| chr8:96692701
|
T | C | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.-35+47299T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692701 | ||||||
| chr8:96692830
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+47428A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692830 | ||||||
| chr8:96692835
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-35+47433C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692835 | ||||||
| chr8:96692999
|
A | G | 1 | a0001c0002t0001g0072 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-35+47597A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96692999 | ||||||
| chr8:96693056
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+47654G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693056 | ||||||
| chr8:96693178
|
A | T | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+47776A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693178 | ||||||
| chr8:96693201
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-35+47799G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693201 | ||||||
| chr8:96693258
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+47856G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693258 | ||||||
| chr8:96693315
|
CAG | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+47917_-35+4791 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96693315 | |||||
| chr8:96693434
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+48032G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693434 | ||||||
| chr8:96693468
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-35+48066A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693468 | ||||||
| chr8:96693509
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+48107G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693509 | ||||||
| chr8:96693530
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-35+48128T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693530 | ||||||
| chr8:96693609
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+48207G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693609 | ||||||
| chr8:96693756
|
T | C | 1 | a0001c0002t0001g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-35+48354T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693756 | ||||||
| chr8:96693785
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+48383G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693785 | ||||||
| chr8:96693839
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-35+48437G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693839 | ||||||
| chr8:96693953
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+48551A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693953 | ||||||
| chr8:96693974
|
C | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG01081.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.-35+48572C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96693974 | ||||||
| chr8:96694006
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+48604G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694006 | ||||||
| chr8:96694039
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+48637C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694039 | ||||||
| chr8:96694132
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-35+48730A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694132 | ||||||
| chr8:96694337
|
T | TAA | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+48946_-35+4894 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96694337 | |||||
| chr8:96694633
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49231A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694633 | ||||||
| chr8:96694648
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35+49246G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694648 | ||||||
| chr8:96694789
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49387G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694789 | ||||||
| chr8:96694822
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0002g0067 | 3 | HG00733.hp1 HG01255.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-35+49420C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694822 | ||||||
| chr8:96694912
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49510G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694912 | ||||||
| chr8:96694920
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-35+49518T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694920 | ||||||
| chr8:96694948
|
G | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49546G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96694948 | ||||||
| chr8:96695052
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49650A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695052 | ||||||
| chr8:96695131
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49729T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695131 | ||||||
| chr8:96695171
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-35+49769G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695171 | ||||||
| chr8:96695209
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+49807T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695209 | ||||||
| chr8:96695498
|
C | T | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+50096C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695498 | ||||||
| chr8:96695520
|
A | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+50118A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695520 | ||||||
| chr8:96695643
|
C | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-35+50241C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695643 | ||||||
| chr8:96695722
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50320A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695722 | ||||||
| chr8:96695726
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50324T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695726 | ||||||
| chr8:96695734
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-35+50332C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695734 | ||||||
| chr8:96695748
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50346T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695748 | ||||||
| chr8:96695764
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-35+50362T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695764 | ||||||
| chr8:96695786
|
G | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0002t0001g0005others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+50384G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695786 | ||||||
| chr8:96695792
|
CAG | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50391_-35+5039 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695792 | ||||||
| chr8:96695818
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50416T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695818 | ||||||
| chr8:96695820
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50418G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695820 | ||||||
| chr8:96695840
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50438A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695840 | ||||||
| chr8:96695864
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50462A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695864 | ||||||
| chr8:96695913
|
T | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.-35+50511T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695913 | ||||||
| chr8:96695930
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50528C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695930 | ||||||
| chr8:96695992
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+50590G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96695992 | ||||||
| chr8:96696004
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+50602T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696004 | ||||||
| chr8:96696106
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+50704C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696106 | ||||||
| chr8:96696128
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+50726T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696128 | ||||||
| chr8:96696295
|
G | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0002t0001g0005others(4): Show | 7 | HG01255.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+50893G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696295 | ||||||
| chr8:96696379
|
CATGTGTA others(3): Show |
C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+50982_-35+5099 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96696379 | |||||
| chr8:96696384
|
G | A | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+50982G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696384 | ||||||
| chr8:96696388
|
G | A | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+50986G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696388 | ||||||
| chr8:96696419
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+51017T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696419 | ||||||
| chr8:96696452
|
T | TAAAAAAA others(5): Show |
1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+51059_-35+5106 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96696452 | |||||
| chr8:96696509
|
A | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+51107A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696509 | ||||||
| chr8:96696566
|
A | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+51164A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696566 | ||||||
| chr8:96696606
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+51204A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696606 | ||||||
| chr8:96696693
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-35+51291C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696693 | ||||||
| chr8:96696755
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+51353C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696755 | ||||||
| chr8:96696876
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+51474A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96696876 | ||||||
| chr8:96697034
|
C | T | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-35+51632C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697034 | ||||||
| chr8:96697301
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+51899T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697301 | ||||||
| chr8:96697627
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+52225A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697627 | ||||||
| chr8:96697628
|
A | G | 4 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0002g0085others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+52226A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697628 | ||||||
| chr8:96697766
|
C | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+52364C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697766 | ||||||
| chr8:96697870
|
A | G | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+52468A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697870 | ||||||
| chr8:96697965
|
G | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+52563G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96697965 | ||||||
| chr8:96698149
|
CAGTT | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+52750_-35+5275 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96698149 | |||||
| chr8:96698152
|
T | A | 2 | a0001c0001t0001g0028a0009c0012t0001g0090 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35+52750T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698152 | ||||||
| chr8:96698153
|
T | C | 2 | a0001c0001t0001g0028a0009c0012t0001g0090 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35+52751T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698153 | ||||||
| chr8:96698285
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+52883G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698285 | ||||||
| chr8:96698413
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+53011T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698413 | ||||||
| chr8:96698617
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+53215A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698617 | ||||||
| chr8:96698690
|
A | G | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-35+53288A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698690 | ||||||
| chr8:96698722
|
T | TA | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+53320_-35+5332 others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698722 | ||||||
| chr8:96698758
|
T | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+53356T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698758 | ||||||
| chr8:96698818
|
T | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.-35+53416T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698818 | ||||||
| chr8:96698827
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+53425A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698827 | ||||||
| chr8:96698907
|
T | C | 28 | a0001c0001t0001g0036a0001c0001t0001g0108a0001c0001t0001g0110others(25): Show | 28 | HG01261.hp2 HG02040.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-35+53505T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96698907 | ||||||
| chr8:96699031
|
C | T | 37 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 37 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.-35+53629C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699031 | ||||||
| chr8:96699087
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+53685T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699087 | ||||||
| chr8:96699125
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+53723T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699125 | ||||||
| chr8:96699313
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+53911T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699313 | ||||||
| chr8:96699415
|
A | C | 2 | a0001c0002t0001g0115a0001c0004t0001g0114 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-35+54013A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699415 | ||||||
| chr8:96699596
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+54194C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699596 | ||||||
| chr8:96699689
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+54287C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699689 | ||||||
| chr8:96699709
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-35+54307C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699709 | ||||||
| chr8:96699719
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-35+54317T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699719 | ||||||
| chr8:96699796
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+54394C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96699796 | ||||||
| chr8:96700081
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+54679A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96700081 | ||||||
| chr8:96700465
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-35+55063G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96700465 | ||||||
| chr8:96700517
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+55115G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96700517 | ||||||
| chr8:96700567
|
CT | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+55167delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96700567 | |||||
| chr8:96700641
|
C | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+55239C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96700641 | ||||||
| chr8:96700901
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+55499A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96700901 | ||||||
| chr8:96700922
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+55520T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96700922 | ||||||
| chr8:96701089
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+55687A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701089 | ||||||
| chr8:96701275
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+55873T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701275 | ||||||
| chr8:96701382
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-35+55980G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701382 | ||||||
| chr8:96701538
|
G | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 40 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.-35+56136G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701538 | ||||||
| chr8:96701539
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56137A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701539 | ||||||
| chr8:96701569
|
A | AT | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56167_-35+5616 others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701569 | ||||||
| chr8:96701575
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0080 | 2 | NA19012.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-35+56173G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701575 | ||||||
| chr8:96701712
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+56310T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701712 | ||||||
| chr8:96701778
|
G | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+56376G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701778 | ||||||
| chr8:96701840
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56438T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701840 | ||||||
| chr8:96701866
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56464A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96701866 | ||||||
| chr8:96702120
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56718G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702120 | ||||||
| chr8:96702318
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56916C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702318 | ||||||
| chr8:96702380
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+56978A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702380 | ||||||
| chr8:96702448
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57046C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702448 | ||||||
| chr8:96702623
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57221G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702623 | ||||||
| chr8:96702638
|
A | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57236A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702638 | ||||||
| chr8:96702802
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+57400T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702802 | ||||||
| chr8:96702971
|
C | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57569C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702971 | ||||||
| chr8:96702996
|
T | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57594T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96702996 | ||||||
| chr8:96703004
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57602T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703004 | ||||||
| chr8:96703109
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57707T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703109 | ||||||
| chr8:96703372
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57970C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703372 | ||||||
| chr8:96703388
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+57986G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703388 | ||||||
| chr8:96703487
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+58085A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703487 | ||||||
| chr8:96703539
|
G | T | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.-35+58137G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703539 | ||||||
| chr8:96703628
|
C | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+58226C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703628 | ||||||
| chr8:96703635
|
C | CTGGGATT others(7): Show |
1 | a0001c0002t0001g0066 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-35+58237_-35+5825 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96703635 | |||||
| chr8:96703668
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0020others(3): Show | 6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+58266A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703668 | ||||||
| chr8:96703775
|
T | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+58373T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703775 | ||||||
| chr8:96703893
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-35+58491G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96703893 | ||||||
| chr8:96704087
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+58685T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704087 | ||||||
| chr8:96704142
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+58740A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704142 | ||||||
| chr8:96704186
|
G | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+58784G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704186 | ||||||
| chr8:96704396
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-35+58994A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704396 | ||||||
| chr8:96704416
|
A | C | 3 | a0001c0001t0001g0028a0001c0002t0002g0004a0009c0012t0001g0090 | 3 | HG02257.hp2 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35+59014A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704416 | ||||||
| chr8:96704416
|
A | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0003c0005t0001g0007 | 3 | HG02280.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-35+59014A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704416 | ||||||
| chr8:96704441
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+59039A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704441 | ||||||
| chr8:96704453
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59051C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704453 | ||||||
| chr8:96704456
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0002g0011a0001c0001t0002g0012others(1): Show | 4 | HG02004.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+59054T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704456 | ||||||
| chr8:96704503
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59101G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704503 | ||||||
| chr8:96704531
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59129A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704531 | ||||||
| chr8:96704538
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59136A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704538 | ||||||
| chr8:96704548
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59146G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704548 | ||||||
| chr8:96704581
|
G | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+59179G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704581 | ||||||
| chr8:96704831
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59429C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704831 | ||||||
| chr8:96704870
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59468T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704870 | ||||||
| chr8:96704999
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+59597G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96704999 | ||||||
| chr8:96705005
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+59603G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705005 | ||||||
| chr8:96705249
|
T | G | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 41 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(38): Show |
intron_variant | MODIFIER | c.-35+59847T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705249 | ||||||
| chr8:96705294
|
T | C | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-35+59892T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705294 | ||||||
| chr8:96705424
|
C | A | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-35+60022C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705424 | ||||||
| chr8:96705537
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+60135A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705537 | ||||||
| chr8:96705708
|
T | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+60306T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705708 | ||||||
| chr8:96705725
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+60323T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96705725 | ||||||
| chr8:96706173
|
T | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+60771T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96706173 | ||||||
| chr8:96706356
|
T | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+60954T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96706356 | ||||||
| chr8:96706417
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+61015C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96706417 | ||||||
| chr8:96706418
|
TG | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0002t0001g0098others(1): Show | 4 | HG02647.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+61018delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96706418 | |||||
| chr8:96706648
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+61246G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96706648 | ||||||
| chr8:96706796
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+61394C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96706796 | ||||||
| chr8:96706831
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+61429A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96706831 | ||||||
| chr8:96707215
|
G | C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-35+61813G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707215 | ||||||
| chr8:96707280
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0019 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-35+61878A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707280 | ||||||
| chr8:96707476
|
T | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+62074T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707476 | ||||||
| chr8:96707543
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+62141G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707543 | ||||||
| chr8:96707663
|
TAATG | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+62287_-35+6229 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96707663 | |||||
| chr8:96707663
|
TAATGAAT others(1): Show |
T | 10 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0112others(7): Show | 10 | HG02040.hp2 HG03927.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+62283_-35+6229 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96707663 | |||||
| chr8:96707688
|
AATGAT | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+62287_-35+6229 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707688 | ||||||
| chr8:96707692
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+62290A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707692 | ||||||
| chr8:96707716
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35+62314C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707716 | ||||||
| chr8:96707752
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-35+62350G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707752 | ||||||
| chr8:96707803
|
T | A | 37 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 37 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.-35+62401T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707803 | ||||||
| chr8:96707945
|
G | T | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-35+62543G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707945 | ||||||
| chr8:96707996
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+62594G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96707996 | ||||||
| chr8:96708150
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+62748A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708150 | ||||||
| chr8:96708226
|
A | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+62824A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708226 | ||||||
| chr8:96708341
|
A | C | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-35+62939A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708341 | ||||||
| chr8:96708419
|
ATG | A | 42 | a0001c0001t0001g0036a0001c0001t0001g0108a0001c0001t0001g0110others(39): Show | 42 | HG01261.hp2 HG01516.hp1 HG01517.hp2 others(39): Show |
intron_variant | MODIFIER | c.-35+63035_-35+6303 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96708419 | |||||
| chr8:96708433
|
GTGTGTA | G | 38 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(35): Show | 38 | HG00099.hp2 HG01081.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+63033_-35+6303 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96708433 | |||||
| chr8:96708435
|
G | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+63033G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708435 | ||||||
| chr8:96708435
|
GTGTATA | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG02004.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+63035_-35+6304 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96708435 | |||||
| chr8:96708437
|
G | A | 12 | a0001c0001t0002g0029a0001c0002t0001g0005a0001c0002t0001g0006others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-35+63035G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708437 | ||||||
| chr8:96708437
|
GTA | G | 27 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(24): Show | 27 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-35+63056_-35+6305 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96708437 | |||||
| chr8:96708441
|
A | G | 2 | a0004c0006t0001g0074a0004c0006t0001g0075 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-35+63039A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708441 | ||||||
| chr8:96708464
|
G | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077 | 3 | NA18945.hp2 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-35+63062G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708464 | ||||||
| chr8:96708798
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+63396C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708798 | ||||||
| chr8:96708799
|
G | A | 38 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(35): Show | 38 | HG00099.hp2 HG01081.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+63397G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96708799 | ||||||
| chr8:96709143
|
T | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+63741T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709143 | ||||||
| chr8:96709145
|
G | T | 2 | a0001c0002t0001g0115a0001c0004t0001g0114 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-35+63743G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709145 | ||||||
| chr8:96709236
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+63834C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709236 | ||||||
| chr8:96709256
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-35+63854T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709256 | ||||||
| chr8:96709258
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+63856C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709258 | ||||||
| chr8:96709423
|
T | TTAGTTCA others(349): Show |
1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-35+64037_-35+6403 others(360): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96709423 | |||||
| chr8:96709643
|
C | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(49): Show | 52 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-35+64241C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709643 | ||||||
| chr8:96709647
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-35+64245A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709647 | ||||||
| chr8:96709840
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-35+64438T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709840 | ||||||
| chr8:96709919
|
T | C | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.-35+64517T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709919 | ||||||
| chr8:96709927
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+64525C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709927 | ||||||
| chr8:96709929
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-35+64527A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96709929 | ||||||
| chr8:96710189
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-35+64787A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96710189 | ||||||
| chr8:96710201
|
A | AT | 25 | a0001c0001t0001g0036a0001c0001t0001g0108a0001c0001t0001g0110others(22): Show | 25 | HG02040.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-35+64807dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96710201 | |||||
| chr8:96710615
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+65213C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96710615 | ||||||
| chr8:96710640
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+65238G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96710640 | ||||||
| chr8:96710743
|
T | C | 1 | a0001c0002t0001g0096 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-35+65341T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96710743 | ||||||
| chr8:96710889
|
G | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0108a0001c0001t0001g0110others(10): Show | 13 | HG02040.hp2 HG02970.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35+65487G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96710889 | ||||||
| chr8:96711025
|
G | T | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.-35+65623G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96711025 | ||||||
| chr8:96711403
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+66001C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96711403 | ||||||
| chr8:96711427
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+66025G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96711427 | ||||||
| chr8:96711574
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+66172T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96711574 | ||||||
| chr8:96711853
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-35+66451T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96711853 | ||||||
| chr8:96712075
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-35+66673C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96712075 | ||||||
| chr8:96712588
|
T | G | 1 | a0001c0002t0001g0066 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-35+67186T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96712588 | ||||||
| chr8:96712747
|
G | T | 2 | a0001c0002t0001g0115a0001c0004t0001g0114 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-35+67345G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96712747 | ||||||
| chr8:96712877
|
A | AT | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+67484dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96712877 | |||||
| chr8:96712905
|
G | A | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+67503G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96712905 | ||||||
| chr8:96712947
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+67545T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96712947 | ||||||
| chr8:96712962
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+67560T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96712962 | ||||||
| chr8:96713188
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+67786C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713188 | ||||||
| chr8:96713246
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+67844A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713246 | ||||||
| chr8:96713288
|
C | G | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-35+67886C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713288 | ||||||
| chr8:96713358
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+67956G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713358 | ||||||
| chr8:96713650
|
T | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.-35+68248T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713650 | ||||||
| chr8:96713665
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+68263G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713665 | ||||||
| chr8:96713679
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-35+68277T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713679 | ||||||
| chr8:96713688
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+68286C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713688 | ||||||
| chr8:96713708
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+68306A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713708 | ||||||
| chr8:96713759
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+68357A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96713759 | ||||||
| chr8:96714053
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-35+68651C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714053 | ||||||
| chr8:96714208
|
G | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+68806G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714208 | ||||||
| chr8:96714320
|
T | G | 1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-35+68918T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714320 | ||||||
| chr8:96714521
|
G | T | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-35+69119G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714521 | ||||||
| chr8:96714622
|
AT | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+69228delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96714622 | |||||
| chr8:96714699
|
G | T | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-35+69297G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714699 | ||||||
| chr8:96714708
|
G | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 40 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.-35+69306G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714708 | ||||||
| chr8:96714788
|
T | G | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 41 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(38): Show |
intron_variant | MODIFIER | c.-35+69386T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714788 | ||||||
| chr8:96714819
|
T | C | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35+69417T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714819 | ||||||
| chr8:96714842
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+69440A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714842 | ||||||
| chr8:96714862
|
G | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+69460G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714862 | ||||||
| chr8:96714920
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-35+69518A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96714920 | ||||||
| chr8:96715071
|
TA | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+69670delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96715071 | ||||||
| chr8:96715083
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-35+69681C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96715083 | ||||||
| chr8:96715171
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-34-69693G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96715171 | ||||||
| chr8:96715517
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-34-69347G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96715517 | ||||||
| chr8:96715563
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-34-69301A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96715563 | ||||||
| chr8:96715783
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-69081C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96715783 | ||||||
| chr8:96716269
|
T | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-68595T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716269 | ||||||
| chr8:96716476
|
C | T | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-68388C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716476 | ||||||
| chr8:96716505
|
A | G | 2 | a0001c0002t0001g0069a0003c0005t0001g0068 | 2 | HG01081.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-34-68359A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716505 | ||||||
| chr8:96716521
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.-34-68343C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716521 | ||||||
| chr8:96716525
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-68339T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716525 | ||||||
| chr8:96716596
|
T | G | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 41 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(38): Show |
intron_variant | MODIFIER | c.-34-68268T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716596 | ||||||
| chr8:96716627
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-68237G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716627 | ||||||
| chr8:96716736
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34-68128C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716736 | ||||||
| chr8:96716737
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-68127G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716737 | ||||||
| chr8:96716755
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-68109A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716755 | ||||||
| chr8:96716817
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-34-68047G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716817 | ||||||
| chr8:96716831
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-68033T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716831 | ||||||
| chr8:96716835
|
A | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG01081.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.-34-68029A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96716835 | ||||||
| chr8:96717024
|
A | AAT | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0110others(10): Show | 13 | HG01516.hp2 HG02109.hp1 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.-34-67788_-34-6778 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATAT | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0002t0001g0002others(7): Show | 10 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-67790_-34-6778 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATATAT | 3 | a0001c0002t0001g0049a0001c0002t0001g0097a0001c0007t0001g0038 | 3 | HG03579.hp2 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-34-67792_-34-6778 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATATATA others(1): Show |
6 | a0001c0002t0001g0066a0001c0002t0001g0086a0001c0002t0001g0093others(3): Show | 6 | HG02257.hp1 HG02809.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-67794_-34-6778 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATATATA others(3): Show |
2 | a0001c0002t0001g0088a0001c0002t0002g0050 | 2 | HG01261.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-34-67796_-34-6778 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATATATA others(5): Show |
2 | a0001c0001t0002g0029a0002c0003t0001g0053 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-34-67798_-34-6778 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATATATA others(7): Show |
1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-34-67800_-34-6778 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
A | AATATATA others(15): Show |
1 | a0001c0002t0003g0001 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-34-67808_-34-6778 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AAT | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0105others(6): Show | 9 | HG02004.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-67788_-34-6778 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATAT | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0033others(12): Show | 15 | HG01081.hp1 HG01261.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34-67790_-34-6778 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATAT | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0002g0011 | 3 | HG00099.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-34-67792_-34-6778 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0002g0020a0001c0001t0002g0024a0001c0001t0002g0100others(1): Show | 4 | HG01975.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-67794_-34-6778 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(3): Show |
A | 5 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0076others(2): Show | 5 | HG02717.hp2 HG02922.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-67796_-34-6778 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(5): Show |
A | 5 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0002t0001g0101others(2): Show | 5 | HG00733.hp2 HG02615.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-67798_-34-6778 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(7): Show |
A | 2 | a0001c0001t0002g0099a0001c0001t0002g0103 | 2 | HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-34-67800_-34-6778 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-34-67802_-34-6778 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(11): Show |
A | 6 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0080others(3): Show | 6 | HG00099.hp1 HG01255.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-67804_-34-6778 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(13): Show |
A | 5 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0070others(2): Show | 5 | HG01978.hp1 HG01978.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-67806_-34-6778 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(15): Show |
A | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG00733.hp1 HG01255.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-67808_-34-6778 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(17): Show |
A | 3 | a0001c0001t0001g0064a0001c0002t0001g0122a0001c0002t0001g0123 | 3 | HG02055.hp1 HG02717.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-34-67810_-34-6778 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(19): Show |
A | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-34-67812_-34-6778 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(21): Show |
A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-67814_-34-6778 others(32): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(29): Show |
A | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-34-67822_-34-6778 others(40): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(31): Show |
A | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-34-67824_-34-6778 others(42): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717024
|
AATATATA others(33): Show |
A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0002t0001g0098others(1): Show | 4 | HG02647.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-67826_-34-6778 others(44): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717024 | |||||
| chr8:96717030
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67834T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717030 | ||||||
| chr8:96717031
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67833A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717031 | ||||||
| chr8:96717041
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67823A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717041 | ||||||
| chr8:96717046
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67818T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717046 | ||||||
| chr8:96717047
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67817A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717047 | ||||||
| chr8:96717051
|
ATATATAT others(21): Show |
A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67804_-34-6777 others(32): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96717051 | |||||
| chr8:96717076
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-34-67788T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717076 | ||||||
| chr8:96717084
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67780T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717084 | ||||||
| chr8:96717086
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67778T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717086 | ||||||
| chr8:96717135
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-67729G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717135 | ||||||
| chr8:96717185
|
CAT | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG01081.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34-67678_-34-6767 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717185 | ||||||
| chr8:96717225
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-67639T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717225 | ||||||
| chr8:96717373
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-67491A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717373 | ||||||
| chr8:96717689
|
C | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-67175C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717689 | ||||||
| chr8:96717778
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-67086C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96717778 | ||||||
| chr8:96718152
|
C | T | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-34-66712C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718152 | ||||||
| chr8:96718216
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-34-66648G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718216 | ||||||
| chr8:96718246
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-66618G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718246 | ||||||
| chr8:96718293
|
A | G | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(81): Show | 84 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.-34-66571A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718293 | ||||||
| chr8:96718588
|
G | C | 36 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(33): Show | 36 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(33): Show |
intron_variant | MODIFIER | c.-34-66276G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718588 | ||||||
| chr8:96718590
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-34-66274G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718590 | ||||||
| chr8:96718667
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-66197C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718667 | ||||||
| chr8:96718869
|
G | T | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-34-65995G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96718869 | ||||||
| chr8:96719362
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-65502G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96719362 | ||||||
| chr8:96719605
|
AGCGAGTG others(3): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-65256_-34-6524 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96719605 | |||||
| chr8:96719733
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-65131C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96719733 | ||||||
| chr8:96719938
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-34-64926C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96719938 | ||||||
| chr8:96720060
|
A | G | 1 | a0001c0002t0002g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-34-64804A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720060 | ||||||
| chr8:96720273
|
T | TA | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-64591_-34-6459 others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720273 | ||||||
| chr8:96720274
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-64590T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720274 | ||||||
| chr8:96720275
|
T | A | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-64589T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720275 | ||||||
| chr8:96720276
|
T | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-64588T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720276 | ||||||
| chr8:96720296
|
G | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.-34-64568G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720296 | ||||||
| chr8:96720326
|
T | A | 40 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 40 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.-34-64538T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720326 | ||||||
| chr8:96720373
|
C | CTA | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-64491_-34-6449 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720373 | ||||||
| chr8:96720619
|
C | T | 37 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 37 | HG00099.hp2 HG01081.hp1 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.-34-64245C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720619 | ||||||
| chr8:96720664
|
TA | T | 24 | a0001c0001t0001g0036a0001c0001t0001g0108a0001c0001t0001g0110others(21): Show | 24 | HG01261.hp2 HG02040.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-34-64196delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96720664 | |||||
| chr8:96720704
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-64160C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720704 | ||||||
| chr8:96720759
|
A | C | 1 | a0003c0005t0001g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-34-64105A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720759 | ||||||
| chr8:96720777
|
G | T | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-34-64087G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720777 | ||||||
| chr8:96720869
|
T | C | 8 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-63995T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96720869 | ||||||
| chr8:96721085
|
C | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0002t0001g0055others(1): Show | 4 | HG01975.hp1 HG01978.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-63779C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721085 | ||||||
| chr8:96721367
|
C | T | 9 | a0001c0002t0001g0049a0001c0002t0001g0058a0001c0002t0001g0065others(6): Show | 9 | NA18945.hp1 NA18990.hp1 NA19005.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-63497C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721367 | ||||||
| chr8:96721410
|
T | C | 2 | a0001c0002t0001g0122a0001c0002t0001g0123 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-34-63454T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721410 | ||||||
| chr8:96721563
|
A | G | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-34-63301A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721563 | ||||||
| chr8:96721571
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-63293T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721571 | ||||||
| chr8:96721633
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-63231T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721633 | ||||||
| chr8:96721739
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-63125T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721739 | ||||||
| chr8:96721793
|
G | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-63071G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721793 | ||||||
| chr8:96721895
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-62969G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96721895 | ||||||
| chr8:96722129
|
T | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-62735T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96722129 | ||||||
| chr8:96722420
|
G | GTT | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-62435_-34-6243 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96722420 | |||||
| chr8:96722453
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-62411G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96722453 | ||||||
| chr8:96722480
|
G | A | 6 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-62384G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96722480 | ||||||
| chr8:96722763
|
C | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0003c0005t0001g0007 | 3 | HG02280.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-62101C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96722763 | ||||||
| chr8:96722838
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-62026C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96722838 | ||||||
| chr8:96723098
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-61766C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723098 | ||||||
| chr8:96723193
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-34-61671T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723193 | ||||||
| chr8:96723262
|
T | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(57): Show | 60 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.-34-61602T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723262 | ||||||
| chr8:96723549
|
T | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-34-61315T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723549 | ||||||
| chr8:96723606
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-61258T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723606 | ||||||
| chr8:96723660
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-61204C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723660 | ||||||
| chr8:96723673
|
C | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-61191C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723673 | ||||||
| chr8:96723694
|
G | A | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-34-61170G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723694 | ||||||
| chr8:96723753
|
T | C | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0005c0013t0001g0043 | 3 | HG01261.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-34-61111T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96723753 | ||||||
| chr8:96723796
|
T | TA | 4 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0002g0085others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-61062dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96723796 | |||||
| chr8:96724080
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-60784A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724080 | ||||||
| chr8:96724286
|
T | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-60578T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724286 | ||||||
| chr8:96724286
|
T | C | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-34-60578T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724286 | ||||||
| chr8:96724368
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-60496A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724368 | ||||||
| chr8:96724380
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-60484A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724380 | ||||||
| chr8:96724406
|
C | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-60458C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724406 | ||||||
| chr8:96724490
|
G | GAC | 5 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0048others(2): Show | 5 | HG00733.hp1 HG01081.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-60339_-34-6033 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96724490 | |||||
| chr8:96724490
|
G | GACAC | 4 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0002t0001g0005others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-60341_-34-6033 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96724490 | |||||
| chr8:96724490
|
G | GACACACA others(1): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0041 | 2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-34-60345_-34-6033 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96724490 | |||||
| chr8:96724490
|
G | GACACACA others(3): Show |
2 | a0001c0001t0001g0042a0001c0002t0002g0004 | 2 | HG00733.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-34-60347_-34-6033 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96724490 | |||||
| chr8:96724490
|
GACAC | G | 52 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0025others(49): Show | 52 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(49): Show |
intron_variant | MODIFIER | c.-34-60341_-34-6033 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96724490 | |||||
| chr8:96724490
|
GACACACA others(3): Show |
G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-60347_-34-6033 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96724490 | |||||
| chr8:96724525
|
A | C | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-34-60339A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724525 | ||||||
| chr8:96724579
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-60285C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724579 | ||||||
| chr8:96724714
|
T | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-60150T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724714 | ||||||
| chr8:96724776
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-60088C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724776 | ||||||
| chr8:96724831
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-60033G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724831 | ||||||
| chr8:96724864
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.-34-60000G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96724864 | ||||||
| chr8:96725426
|
G | A | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.-34-59438G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725426 | ||||||
| chr8:96725446
|
A | G | 3 | a0001c0001t0001g0110a0001c0007t0001g0038a0006c0010t0001g0045 | 3 | HG02004.hp2 HG03579.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-34-59418A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725446 | ||||||
| chr8:96725485
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-59379G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725485 | ||||||
| chr8:96725528
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-59336G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725528 | ||||||
| chr8:96725599
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-59265C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725599 | ||||||
| chr8:96725717
|
G | A | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.-34-59147G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725717 | ||||||
| chr8:96725902
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-58962C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725902 | ||||||
| chr8:96725919
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-58945T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725919 | ||||||
| chr8:96725965
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-58899A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96725965 | ||||||
| chr8:96726275
|
CATT | C | 17 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(14): Show | 17 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34-58586_-34-5858 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96726275 | |||||
| chr8:96726292
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-58572T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726292 | ||||||
| chr8:96726435
|
C | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-34-58429C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726435 | ||||||
| chr8:96726458
|
T | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-58406T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726458 | ||||||
| chr8:96726502
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-58362T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726502 | ||||||
| chr8:96726694
|
C | A | 1 | a0001c0002t0001g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-34-58170C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726694 | ||||||
| chr8:96726819
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-58045T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726819 | ||||||
| chr8:96726838
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-58026T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96726838 | ||||||
| chr8:96726873
|
A | ACACCAGC others(11): Show |
2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-57985_-34-5798 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96726873 | |||||
| chr8:96727005
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-34-57859T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727005 | ||||||
| chr8:96727068
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-57796G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727068 | ||||||
| chr8:96727160
|
A | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-57704A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727160 | ||||||
| chr8:96727180
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0125a0001c0001t0002g0021others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-57684A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727180 | ||||||
| chr8:96727374
|
A | G | 4 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(1): Show | 4 | HG02630.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-57490A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727374 | ||||||
| chr8:96727386
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-57478C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727386 | ||||||
| chr8:96727816
|
T | C | 2 | a0002c0003t0001g0008a0002c0003t0001g0015 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34-57048T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727816 | ||||||
| chr8:96727932
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34-56932C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727932 | ||||||
| chr8:96727980
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-56884G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96727980 | ||||||
| chr8:96728039
|
C | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-56825C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728039 | ||||||
| chr8:96728061
|
T | C | 1 | a0001c0002t0002g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-34-56803T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728061 | ||||||
| chr8:96728114
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-56750C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728114 | ||||||
| chr8:96728533
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-56331A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728533 | ||||||
| chr8:96728676
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-34-56188A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728676 | ||||||
| chr8:96728757
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-56107G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728757 | ||||||
| chr8:96728843
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34-56021G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728843 | ||||||
| chr8:96728942
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-55922A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728942 | ||||||
| chr8:96728985
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-55879A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96728985 | ||||||
| chr8:96729450
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-55414A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729450 | ||||||
| chr8:96729520
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-55344A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729520 | ||||||
| chr8:96729694
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-55170T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729694 | ||||||
| chr8:96729718
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-34-55146A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729718 | ||||||
| chr8:96729731
|
T | C | 2 | a0001c0002t0001g0120a0001c0002t0001g0121 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-34-55133T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729731 | ||||||
| chr8:96729743
|
G | A | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-34-55121G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729743 | ||||||
| chr8:96729855
|
T | TTG | 22 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(19): Show | 22 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-54997_-34-5499 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96729855 | |||||
| chr8:96729966
|
A | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-54898A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729966 | ||||||
| chr8:96729978
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-54886A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96729978 | ||||||
| chr8:96730110
|
G | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-54754G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96730110 | ||||||
| chr8:96730345
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-54519C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96730345 | ||||||
| chr8:96730423
|
A | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-54441A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96730423 | ||||||
| chr8:96730866
|
C | CAT | 5 | a0001c0002t0001g0098a0001c0002t0001g0124a0001c0004t0001g0114others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-53973_-34-5397 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(15): Show |
1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-34-53995_-34-5399 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-34-53995_-34-5399 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(5): Show |
1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-34-53995_-34-5399 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(9): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0057others(1): Show | 4 | HG01943.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-53995_-34-5399 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(11): Show |
11 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0035others(8): Show | 11 | HG01516.hp2 HG01975.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34-53995_-34-5399 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(13): Show |
12 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0063others(9): Show | 12 | HG00733.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-53995_-34-5399 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(15): Show |
14 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0032others(11): Show | 14 | HG02040.hp1 HG02723.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34-53995_-34-5399 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(17): Show |
11 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0056others(8): Show | 11 | HG00099.hp1 HG01884.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34-53995_-34-5399 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATACATA others(19): Show |
1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-53995_-34-5399 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATAT | 3 | a0001c0002t0001g0121a0001c0002t0002g0085a0006c0010t0001g0045 | 3 | HG02004.hp2 HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-34-53975_-34-5397 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(1): Show |
2 | a0001c0002t0001g0120a0001c0008t0001g0116 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-34-53979_-34-5397 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(5): Show |
1 | a0001c0002t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-34-53983_-34-5397 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(9): Show |
1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-34-53987_-34-5397 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(17): Show |
1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-34-53995_-34-5397 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(19): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0002t0001g0040 | 3 | HG01261.hp2 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-34-53997_-34-5397 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(21): Show |
2 | a0001c0001t0001g0010a0001c0002t0001g0122 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-34-53972_-34-5397 others(32): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
C | CATATATA others(23): Show |
1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-34-53972_-34-5397 others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
CAT | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0102a0001c0001t0001g0109others(1): Show | 4 | HG00099.hp2 NA19005.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-53973_-34-5397 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730866
|
CATATATA others(5): Show |
C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-53983_-34-5397 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730866 | |||||
| chr8:96730868
|
T | TAC | 2 | a0001c0001t0001g0028a0001c0001t0002g0029 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-34-53995_-34-5399 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730868 | |||||
| chr8:96730872
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0102a0001c0001t0001g0109 | 3 | HG00099.hp2 NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-34-53992T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96730872 | ||||||
| chr8:96730895
|
AT | A | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(23): Show | 26 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-34-53960delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96730895 | |||||
| chr8:96730903
|
T | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-53961T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96730903 | ||||||
| chr8:96730904
|
T | A | 4 | a0001c0001t0001g0056a0001c0002t0001g0055a0001c0002t0001g0059others(1): Show | 4 | HG01975.hp1 HG01978.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-53960T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96730904 | ||||||
| chr8:96731045
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-53819C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731045 | ||||||
| chr8:96731074
|
C | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-53790C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731074 | ||||||
| chr8:96731210
|
G | T | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.-34-53654G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731210 | ||||||
| chr8:96731217
|
A | ATACC | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-53645_-34-5364 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96731217 | |||||
| chr8:96731484
|
G | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-53380G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731484 | ||||||
| chr8:96731732
|
G | C | 1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-34-53132G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731732 | ||||||
| chr8:96731831
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-34-53033A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731831 | ||||||
| chr8:96731869
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-52995G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731869 | ||||||
| chr8:96731871
|
T | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-52993T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96731871 | ||||||
| chr8:96732197
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-52667A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96732197 | ||||||
| chr8:96732388
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-52476C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96732388 | ||||||
| chr8:96732566
|
TTTC | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0056others(6): Show | 9 | HG00733.hp1 HG01975.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-52295_-34-5229 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96732566 | |||||
| chr8:96732567
|
TTC | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.-34-52295_-34-5229 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96732567 | |||||
| chr8:96732605
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-52259T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96732605 | ||||||
| chr8:96732707
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-34-52157C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96732707 | ||||||
| chr8:96732966
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-51898A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96732966 | ||||||
| chr8:96733109
|
A | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-51755A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96733109 | ||||||
| chr8:96733142
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-34-51722A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96733142 | ||||||
| chr8:96733254
|
C | G | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-51610C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96733254 | ||||||
| chr8:96733447
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-51417C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96733447 | ||||||
| chr8:96734039
|
C | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-50825C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734039 | ||||||
| chr8:96734063
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-50801G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734063 | ||||||
| chr8:96734330
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-50534C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734330 | ||||||
| chr8:96734399
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-50465A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734399 | ||||||
| chr8:96734440
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-50424G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734440 | ||||||
| chr8:96734539
|
A | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34-50325A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734539 | ||||||
| chr8:96734560
|
A | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-50304A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734560 | ||||||
| chr8:96734582
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-50282G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734582 | ||||||
| chr8:96734711
|
AAAAAT | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34-50129_-34-5012 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96734711 | |||||
| chr8:96734897
|
G | T | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-34-49967G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734897 | ||||||
| chr8:96734968
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-49896C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96734968 | ||||||
| chr8:96735247
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-49617G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735247 | ||||||
| chr8:96735371
|
C | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-49493C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735371 | ||||||
| chr8:96735481
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-49383A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735481 | ||||||
| chr8:96735558
|
A | G | 3 | a0001c0002t0001g0123a0001c0007t0001g0038a0003c0005t0001g0007 | 3 | HG02717.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-49306A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735558 | ||||||
| chr8:96735689
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-34-49175C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735689 | ||||||
| chr8:96735720
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-34-49144G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735720 | ||||||
| chr8:96735735
|
C | T | 61 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.-34-49129C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735735 | ||||||
| chr8:96735978
|
A | T | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-34-48886A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96735978 | ||||||
| chr8:96736101
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-48763C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96736101 | ||||||
| chr8:96736113
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-48751T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96736113 | ||||||
| chr8:96736268
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-48596A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96736268 | ||||||
| chr8:96736380
|
A | G | 1 | a0001c0002t0001g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-34-48484A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96736380 | ||||||
| chr8:96736484
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-34-48380A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96736484 | ||||||
| chr8:96737015
|
G | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-47849G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737015 | ||||||
| chr8:96737098
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-34-47766T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737098 | ||||||
| chr8:96737230
|
T | TACAC | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-47612_-34-4760 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737230 | |||||
| chr8:96737230
|
TAC | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34-47610_-34-4760 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737230 | |||||
| chr8:96737248
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-47616C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737248 | ||||||
| chr8:96737250
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-47614C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737250 | ||||||
| chr8:96737252
|
C | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0080others(6): Show | 9 | HG02280.hp1 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-47612C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737252 | ||||||
| chr8:96737253
|
AC | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 15 | HG01884.hp1 HG02004.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34-47610delC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737253 | ||||||
| chr8:96737254
|
C | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0026others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-34-47610C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737254 | ||||||
| chr8:96737256
|
A | C | 2 | a0001c0002t0001g0025a0005c0013t0001g0043 | 2 | NA18522.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-34-47608A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737256 | ||||||
| chr8:96737309
|
G | GAT | 4 | a0001c0001t0001g0110a0001c0002t0001g0040a0001c0002t0001g0079others(1): Show | 4 | HG01261.hp2 HG01943.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-47537_-34-4753 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737309 | |||||
| chr8:96737309
|
GAT | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(7): Show | 10 | HG00733.hp2 HG02004.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-47537_-34-4753 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737309 | |||||
| chr8:96737325
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-34-47539T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737325 | ||||||
| chr8:96737327
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(6): Show | 9 | HG00733.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-47537T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737327 | ||||||
| chr8:96737336
|
T | A | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-34-47528T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737336 | ||||||
| chr8:96737355
|
G | GATATATA others(5): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0077a0001c0001t0001g0078others(1): Show | 4 | HG02615.hp2 HG02965.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-47506_-34-4749 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(7): Show |
14 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0027others(11): Show | 14 | HG01517.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34-47508_-34-4749 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(9): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0031others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(11): Show |
10 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0036others(7): Show | 10 | HG01081.hp1 HG01255.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(13): Show |
4 | a0001c0001t0002g0012a0001c0002t0001g0055a0001c0002t0001g0084others(1): Show | 4 | HG01978.hp1 HG02004.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(15): Show |
2 | a0001c0001t0001g0056a0001c0007t0001g0038 | 2 | HG01978.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(17): Show |
1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-34-47495_-34-4749 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(19): Show |
1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-34-47495_-34-4749 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(23): Show |
1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-34-47495_-34-4749 others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(25): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0002t0001g0005others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(36): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(27): Show |
2 | a0001c0001t0001g0110a0006c0010t0001g0045 | 2 | HG02004.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(38): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(29): Show |
1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-47495_-34-4749 others(40): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737355
|
G | GATATATA others(33): Show |
2 | a0001c0001t0001g0010a0001c0002t0001g0006 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-34-47495_-34-4749 others(44): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737355 | |||||
| chr8:96737508
|
T | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-47356T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737508 | ||||||
| chr8:96737707
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-47157C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737707 | ||||||
| chr8:96737713
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-47151G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737713 | ||||||
| chr8:96737714
|
TC | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-34-47148delC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737714 | |||||
| chr8:96737744
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-47120T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737744 | ||||||
| chr8:96737786
|
CTTA | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-47073_-34-4707 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96737786 | |||||
| chr8:96737823
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-47041C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737823 | ||||||
| chr8:96737885
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-46979A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96737885 | ||||||
| chr8:96738176
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-46688G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96738176 | ||||||
| chr8:96738421
|
GTAGT | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-46440_-34-4643 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96738421 | |||||
| chr8:96738565
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-46299T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96738565 | ||||||
| chr8:96738729
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-46135T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96738729 | ||||||
| chr8:96738767
|
G | A | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-34-46097G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96738767 | ||||||
| chr8:96738922
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-45942G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96738922 | ||||||
| chr8:96738974
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-34-45890C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96738974 | ||||||
| chr8:96739133
|
A | C | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-45731A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739133 | ||||||
| chr8:96739164
|
G | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-45700G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739164 | ||||||
| chr8:96739312
|
GT | G | 17 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(14): Show | 17 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34-45545delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96739312 | |||||
| chr8:96739334
|
T | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-45530T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739334 | ||||||
| chr8:96739385
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-34-45479T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739385 | ||||||
| chr8:96739436
|
C | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-45428C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739436 | ||||||
| chr8:96739546
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-45318T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739546 | ||||||
| chr8:96739550
|
G | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-45314G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739550 | ||||||
| chr8:96739558
|
A | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-45306A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739558 | ||||||
| chr8:96739705
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-45159G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739705 | ||||||
| chr8:96739733
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-45131G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739733 | ||||||
| chr8:96739743
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-45121C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739743 | ||||||
| chr8:96739819
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-45045A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739819 | ||||||
| chr8:96739868
|
A | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-44996A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739868 | ||||||
| chr8:96739903
|
C | G | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-44961C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739903 | ||||||
| chr8:96739942
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-44922C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96739942 | ||||||
| chr8:96740016
|
C | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-44848C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740016 | ||||||
| chr8:96740313
|
T | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-44551T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740313 | ||||||
| chr8:96740316
|
T | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-44548T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740316 | ||||||
| chr8:96740402
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-34-44462C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740402 | ||||||
| chr8:96740411
|
G | A | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-44453G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740411 | ||||||
| chr8:96740414
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-44450A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740414 | ||||||
| chr8:96740536
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-44328A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740536 | ||||||
| chr8:96740593
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-44271G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740593 | ||||||
| chr8:96740673
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-44191G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740673 | ||||||
| chr8:96740702
|
A | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-44162A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740702 | ||||||
| chr8:96740776
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-44088T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740776 | ||||||
| chr8:96740787
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-34-44077C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740787 | ||||||
| chr8:96740809
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-44055A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740809 | ||||||
| chr8:96740843
|
G | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-44021G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740843 | ||||||
| chr8:96740863
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34-44001G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740863 | ||||||
| chr8:96740888
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-43976C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740888 | ||||||
| chr8:96740911
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-43953G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740911 | ||||||
| chr8:96740947
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-43917A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96740947 | ||||||
| chr8:96741126
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-43738C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741126 | ||||||
| chr8:96741229
|
A | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-43635A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741229 | ||||||
| chr8:96741296
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-43568C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741296 | ||||||
| chr8:96741390
|
G | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-43474G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741390 | ||||||
| chr8:96741430
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-43434C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741430 | ||||||
| chr8:96741437
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-43427G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741437 | ||||||
| chr8:96741452
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-34-43412G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741452 | ||||||
| chr8:96741547
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-43317A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741547 | ||||||
| chr8:96741671
|
T | G | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-34-43193T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741671 | ||||||
| chr8:96741717
|
T | C | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-34-43147T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741717 | ||||||
| chr8:96741725
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-43139G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741725 | ||||||
| chr8:96741762
|
A | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-43102A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741762 | ||||||
| chr8:96741895
|
C | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-42969C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741895 | ||||||
| chr8:96741977
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-42887G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741977 | ||||||
| chr8:96741984
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-42880A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96741984 | ||||||
| chr8:96742021
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-42843G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742021 | ||||||
| chr8:96742025
|
A | G | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-34-42839A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742025 | ||||||
| chr8:96742098
|
G | A | 25 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(22): Show | 25 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-34-42766G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742098 | ||||||
| chr8:96742166
|
G | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-42698G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742166 | ||||||
| chr8:96742257
|
G | T | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-34-42607G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742257 | ||||||
| chr8:96742389
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-34-42475T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742389 | ||||||
| chr8:96742408
|
A | T | 21 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(18): Show | 21 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-34-42456A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742408 | ||||||
| chr8:96742417
|
G | T | 1 | a0001c0002t0001g0066 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-34-42447G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742417 | ||||||
| chr8:96742425
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(6): Show | 9 | HG00733.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-42439A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742425 | ||||||
| chr8:96742502
|
G | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-42362G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742502 | ||||||
| chr8:96742629
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-42235A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742629 | ||||||
| chr8:96742726
|
A | C | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-34-42138A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96742726 | ||||||
| chr8:96743141
|
G | A | 58 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-34-41723G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743141 | ||||||
| chr8:96743168
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-41696C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743168 | ||||||
| chr8:96743209
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-41655G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743209 | ||||||
| chr8:96743237
|
C | T | 5 | a0001c0001t0001g0028a0001c0002t0001g0005a0001c0002t0001g0006others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-41627C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743237 | ||||||
| chr8:96743263
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-41601C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743263 | ||||||
| chr8:96743264
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-41600G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743264 | ||||||
| chr8:96743266
|
A | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-41598A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743266 | ||||||
| chr8:96743364
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-41500G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743364 | ||||||
| chr8:96743492
|
C | T | 55 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-34-41372C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743492 | ||||||
| chr8:96743493
|
A | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34-41371A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743493 | ||||||
| chr8:96743613
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-41251A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743613 | ||||||
| chr8:96743614
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-41250C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743614 | ||||||
| chr8:96743815
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-34-41049C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743815 | ||||||
| chr8:96743851
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-34-41013G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743851 | ||||||
| chr8:96743880
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-40984G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96743880 | ||||||
| chr8:96744121
|
C | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-40743C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744121 | ||||||
| chr8:96744134
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-40730T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744134 | ||||||
| chr8:96744151
|
G | A | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-40713G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744151 | ||||||
| chr8:96744248
|
G | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-40616G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744248 | ||||||
| chr8:96744271
|
A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-40593A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744271 | ||||||
| chr8:96744273
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-40591G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744273 | ||||||
| chr8:96744304
|
C | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | NA18747.hp1 NA18962.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-40560C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744304 | ||||||
| chr8:96744313
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-40551C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744313 | ||||||
| chr8:96744339
|
G | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-40525G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744339 | ||||||
| chr8:96744349
|
C | T | 4 | a0001c0002t0001g0066a0001c0002t0001g0101a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02965.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-40515C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744349 | ||||||
| chr8:96744360
|
A | C | 1 | a0004c0006t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34-40504A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744360 | ||||||
| chr8:96744362
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-40502C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744362 | ||||||
| chr8:96744440
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-40424C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744440 | ||||||
| chr8:96744443
|
C | T | 10 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-40421C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744443 | ||||||
| chr8:96744444
|
G | A | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-34-40420G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744444 | ||||||
| chr8:96744457
|
G | A | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-40407G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744457 | ||||||
| chr8:96744482
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-40382C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744482 | ||||||
| chr8:96744615
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0024others(2): Show | 5 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-40249A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744615 | ||||||
| chr8:96744630
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-40234G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744630 | ||||||
| chr8:96744848
|
C | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-40016C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744848 | ||||||
| chr8:96744969
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-39895C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96744969 | ||||||
| chr8:96745133
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-39731T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96745133 | ||||||
| chr8:96745250
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-39614G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96745250 | ||||||
| chr8:96745443
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-39421A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96745443 | ||||||
| chr8:96745919
|
C | T | 5 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(2): Show | 5 | NA18747.hp1 NA18949.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-38945C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96745919 | ||||||
| chr8:96746301
|
A | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-38563A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96746301 | ||||||
| chr8:96746323
|
A | T | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-34-38541A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96746323 | ||||||
| chr8:96746575
|
G | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-38289G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96746575 | ||||||
| chr8:96746615
|
G | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-38249G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96746615 | ||||||
| chr8:96746957
|
A | G | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-37907A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96746957 | ||||||
| chr8:96746991
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-37873G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96746991 | ||||||
| chr8:96747117
|
G | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-37747G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96747117 | ||||||
| chr8:96747158
|
G | A | 1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-34-37706G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96747158 | ||||||
| chr8:96747290
|
C | CA | 9 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0063others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-37556dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96747290 | |||||
| chr8:96747290
|
CA | C | 12 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0064others(9): Show | 12 | HG01261.hp2 HG01981.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34-37556delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96747290 | |||||
| chr8:96747290
|
CAA | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(6): Show | 9 | HG00733.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-37557_-34-3755 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96747290 | |||||
| chr8:96747291
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-37573A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96747291 | ||||||
| chr8:96747308
|
A | C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-37556A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96747308 | ||||||
| chr8:96747862
|
T | G | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-34-37002T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96747862 | ||||||
| chr8:96747924
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-36940C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96747924 | ||||||
| chr8:96748572
|
C | A | 2 | a0001c0001t0001g0064a0001c0002t0001g0111 | 2 | NA19057.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-34-36292C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96748572 | ||||||
| chr8:96748718
|
G | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-36146G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96748718 | ||||||
| chr8:96748837
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-36027G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96748837 | ||||||
| chr8:96749206
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-35658G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749206 | ||||||
| chr8:96749288
|
G | GGAAATAG others(7): Show |
2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-34-35576_-34-3557 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749288 | ||||||
| chr8:96749289
|
C | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-34-35575C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749289 | ||||||
| chr8:96749422
|
C | G | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-34-35442C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749422 | ||||||
| chr8:96749458
|
A | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-35406A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749458 | ||||||
| chr8:96749573
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-35291C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749573 | ||||||
| chr8:96749698
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-35166T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96749698 | ||||||
| chr8:96750151
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-34713A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96750151 | ||||||
| chr8:96750557
|
G | T | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-34307G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96750557 | ||||||
| chr8:96750793
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-34071G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96750793 | ||||||
| chr8:96750837
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-34027C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96750837 | ||||||
| chr8:96750867
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-33997A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96750867 | ||||||
| chr8:96751000
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-33864T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751000 | ||||||
| chr8:96751134
|
T | C | 3 | a0001c0002t0001g0123a0001c0007t0001g0038a0003c0005t0001g0007 | 3 | HG02717.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-33730T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751134 | ||||||
| chr8:96751275
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-34-33589T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751275 | ||||||
| chr8:96751306
|
T | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-33558T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751306 | ||||||
| chr8:96751338
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-34-33526A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751338 | ||||||
| chr8:96751421
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-33443T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751421 | ||||||
| chr8:96751489
|
A | T | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-34-33375A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751489 | ||||||
| chr8:96751542
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-33322C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751542 | ||||||
| chr8:96751599
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-33265C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751599 | ||||||
| chr8:96751958
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-32906T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96751958 | ||||||
| chr8:96752029
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34-32835G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752029 | ||||||
| chr8:96752175
|
G | A | 2 | a0004c0006t0001g0074a0004c0006t0001g0075 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-32689G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752175 | ||||||
| chr8:96752394
|
G | A | 17 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(14): Show | 17 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34-32470G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752394 | ||||||
| chr8:96752422
|
T | C | 27 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(24): Show | 27 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34-32442T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752422 | ||||||
| chr8:96752491
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-34-32373T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752491 | ||||||
| chr8:96752602
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-34-32262A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752602 | ||||||
| chr8:96752756
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-32108C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752756 | ||||||
| chr8:96752760
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-32104G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752760 | ||||||
| chr8:96752804
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-32060C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96752804 | ||||||
| chr8:96753156
|
G | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-31708G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753156 | ||||||
| chr8:96753175
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-31689T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753175 | ||||||
| chr8:96753479
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-31385G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753479 | ||||||
| chr8:96753501
|
TTTGTTTA others(128): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-31361_-34-3122 others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96753501 | |||||
| chr8:96753535
|
A | G | 3 | a0001c0002t0001g0123a0001c0007t0001g0038a0003c0005t0001g0007 | 3 | HG02717.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-31329A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753535 | ||||||
| chr8:96753637
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-31227T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753637 | ||||||
| chr8:96753640
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-31224G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753640 | ||||||
| chr8:96753641
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-31223T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753641 | ||||||
| chr8:96753642
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-31222A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753642 | ||||||
| chr8:96753676
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-31188T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753676 | ||||||
| chr8:96753969
|
T | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0113 | 2 | NA18747.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-34-30895T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753969 | ||||||
| chr8:96753995
|
C | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-30869C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96753995 | ||||||
| chr8:96754068
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-34-30796C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754068 | ||||||
| chr8:96754473
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-30391G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754473 | ||||||
| chr8:96754593
|
T | C | 8 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0108others(5): Show | 8 | HG01975.hp2 HG01981.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-30271T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754593 | ||||||
| chr8:96754606
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-30258G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754606 | ||||||
| chr8:96754684
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-30180T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754684 | ||||||
| chr8:96754737
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-30127A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754737 | ||||||
| chr8:96754764
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-30100A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754764 | ||||||
| chr8:96754821
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-30043G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96754821 | ||||||
| chr8:96755318
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-29546G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96755318 | ||||||
| chr8:96755405
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-29459A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96755405 | ||||||
| chr8:96755721
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-29143A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96755721 | ||||||
| chr8:96755828
|
G | T | 3 | a0001c0007t0001g0038a0006c0010t0001g0045a0009c0012t0001g0090 | 3 | HG02004.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-29036G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96755828 | ||||||
| chr8:96755960
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-28904A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96755960 | ||||||
| chr8:96756093
|
A | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-28771A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96756093 | ||||||
| chr8:96756334
|
A | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-34-28530A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96756334 | ||||||
| chr8:96756739
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-28125T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96756739 | ||||||
| chr8:96756853
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-28011T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96756853 | ||||||
| chr8:96756874
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-27990C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96756874 | ||||||
| chr8:96756908
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-27956C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96756908 | ||||||
| chr8:96757001
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-27863T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757001 | ||||||
| chr8:96757211
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-34-27653C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757211 | ||||||
| chr8:96757240
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-27624A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757240 | ||||||
| chr8:96757354
|
G | GATA | 6 | a0001c0001t0001g0041a0001c0002t0001g0073a0001c0002t0001g0091others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-27465_-34-2746 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96757354 | |||||
| chr8:96757354
|
GATA | G | 27 | a0001c0001t0001g0108a0001c0002t0001g0002a0001c0002t0001g0003others(24): Show | 27 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34-27465_-34-2746 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96757354 | |||||
| chr8:96757354
|
GATAATA | G | 10 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0057others(7): Show | 10 | HG01261.hp2 HG01516.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-27468_-34-2746 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96757354 | |||||
| chr8:96757354
|
GATAATAA others(2): Show |
G | 49 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-34-27471_-34-2746 others(13): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96757354 | |||||
| chr8:96757354
|
GATAATAA others(5): Show |
G | 8 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0078others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-27474_-34-2746 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96757354 | |||||
| chr8:96757354
|
GATAATAA others(8): Show |
G | 2 | a0001c0001t0001g0028a0001c0007t0001g0038 | 2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-27477_-34-2746 others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96757354 | |||||
| chr8:96757360
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-27504A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757360 | ||||||
| chr8:96757545
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-27319T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757545 | ||||||
| chr8:96757547
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-27317C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757547 | ||||||
| chr8:96757559
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-27305A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757559 | ||||||
| chr8:96757686
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-27178A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757686 | ||||||
| chr8:96757907
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-26957A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96757907 | ||||||
| chr8:96758131
|
C | CTAAAT | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-26733_-34-2673 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758131 | ||||||
| chr8:96758132
|
C | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-26732C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758132 | ||||||
| chr8:96758308
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-26556C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758308 | ||||||
| chr8:96758455
|
A | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-26409A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758455 | ||||||
| chr8:96758502
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-26362C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758502 | ||||||
| chr8:96758563
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-26301G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758563 | ||||||
| chr8:96758775
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-26089T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758775 | ||||||
| chr8:96758827
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-26037C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96758827 | ||||||
| chr8:96759135
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-25729C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96759135 | ||||||
| chr8:96759480
|
T | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-34-25384T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96759480 | ||||||
| chr8:96759667
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-25197A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96759667 | ||||||
| chr8:96759699
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-25165C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96759699 | ||||||
| chr8:96760388
|
G | A | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-34-24476G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760388 | ||||||
| chr8:96760441
|
C | T | 8 | a0002c0003t0001g0008a0002c0003t0001g0015a0002c0003t0001g0052others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-24423C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760441 | ||||||
| chr8:96760570
|
A | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-24294A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760570 | ||||||
| chr8:96760691
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-24173G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760691 | ||||||
| chr8:96760742
|
G | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-24122G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760742 | ||||||
| chr8:96760770
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-34-24094A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760770 | ||||||
| chr8:96760798
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-34-24066C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96760798 | ||||||
| chr8:96761187
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-23677T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96761187 | ||||||
| chr8:96761240
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-23624G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96761240 | ||||||
| chr8:96761320
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-23544G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96761320 | ||||||
| chr8:96762152
|
AG | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-34-22711delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96762152 | ||||||
| chr8:96762187
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-22677C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96762187 | ||||||
| chr8:96762329
|
C | T | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-34-22535C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96762329 | ||||||
| chr8:96762423
|
T | C | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-34-22441T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96762423 | ||||||
| chr8:96762434
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-22430A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96762434 | ||||||
| chr8:96762767
|
T | G | 1 | a0001c0002t0001g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-34-22097T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96762767 | ||||||
| chr8:96763096
|
C | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-21768C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96763096 | ||||||
| chr8:96763316
|
A | G | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-34-21548A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96763316 | ||||||
| chr8:96763897
|
A | G | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-20967A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96763897 | ||||||
| chr8:96763966
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0020others(2): Show | 5 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-20898C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96763966 | ||||||
| chr8:96764049
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-20815G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764049 | ||||||
| chr8:96764147
|
A | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-20717A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764147 | ||||||
| chr8:96764718
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-20146G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764718 | ||||||
| chr8:96764750
|
T | A | 55 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-34-20114T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764750 | ||||||
| chr8:96764823
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-20041C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764823 | ||||||
| chr8:96764877
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-19987C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764877 | ||||||
| chr8:96764899
|
A | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-19965A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96764899 | ||||||
| chr8:96765144
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-19720G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96765144 | ||||||
| chr8:96765152
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-19712C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96765152 | ||||||
| chr8:96765545
|
ATTTAT | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-34-19315_-34-1931 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96765545 | |||||
| chr8:96765577
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-34-19287C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96765577 | ||||||
| chr8:96765670
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-34-19194T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96765670 | ||||||
| chr8:96765724
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-19140C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96765724 | ||||||
| chr8:96765775
|
C | T | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-34-19089C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96765775 | ||||||
| chr8:96766074
|
A | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-18790A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766074 | ||||||
| chr8:96766118
|
C | G | 28 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(25): Show | 28 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34-18746C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766118 | ||||||
| chr8:96766179
|
A | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-18685A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766179 | ||||||
| chr8:96766503
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-18361T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766503 | ||||||
| chr8:96766833
|
A | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-18031A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766833 | ||||||
| chr8:96766842
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-18022A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766842 | ||||||
| chr8:96766877
|
GCT | G | 6 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-17982_-34-1798 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96766877 | |||||
| chr8:96766999
|
A | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-17865A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96766999 | ||||||
| chr8:96767235
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-17629G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767235 | ||||||
| chr8:96767291
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-17573A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767291 | ||||||
| chr8:96767493
|
C | CTT | 119 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34-17360_-34-1735 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767493 | |||||
| chr8:96767548
|
T | C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-17316T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767548 | ||||||
| chr8:96767577
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-34-17287A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767577 | ||||||
| chr8:96767635
|
C | CT | 6 | a0001c0001t0001g0102a0001c0001t0001g0109a0001c0002t0001g0040others(3): Show | 6 | HG01261.hp2 HG02055.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-17203dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767635 | |||||
| chr8:96767635
|
C | CTT | 22 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(19): Show | 22 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-17204_-34-1720 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767635 | |||||
| chr8:96767635
|
C | CTTT | 6 | a0001c0002t0001g0119a0001c0002t0001g0124a0001c0004t0001g0107others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-17205_-34-1720 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767635 | |||||
| chr8:96767635
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-17219_-34-1720 others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767635 | |||||
| chr8:96767635
|
CT | C | 51 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-34-17203delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767635 | |||||
| chr8:96767635
|
CTT | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0031others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-17204_-34-1720 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96767635 | |||||
| chr8:96767829
|
G | A | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-17035G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767829 | ||||||
| chr8:96767842
|
A | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-17022A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767842 | ||||||
| chr8:96767998
|
G | A | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.-34-16866G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96767998 | ||||||
| chr8:96768039
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-16825C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96768039 | ||||||
| chr8:96768288
|
C | CT | 27 | a0001c0002t0001g0040a0001c0002t0001g0071a0001c0002t0001g0072others(24): Show | 27 | HG01261.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34-16562dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96768288 | |||||
| chr8:96768318
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-34-16546T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96768318 | ||||||
| chr8:96768319
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-16545G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96768319 | ||||||
| chr8:96768938
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-15926G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96768938 | ||||||
| chr8:96769205
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-34-15659C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769205 | ||||||
| chr8:96769253
|
T | C | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-15611T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769253 | ||||||
| chr8:96769412
|
G | T | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-34-15452G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769412 | ||||||
| chr8:96769488
|
A | G | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-15376A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769488 | ||||||
| chr8:96769532
|
G | C | 1 | a0001c0002t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-34-15332G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769532 | ||||||
| chr8:96769626
|
A | AT | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(7): Show | 10 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-15215dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96769626 | |||||
| chr8:96769626
|
AT | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0046others(12): Show | 15 | HG01884.hp1 HG01943.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34-15215delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96769626 | |||||
| chr8:96769638
|
T | C | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-34-15226T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769638 | ||||||
| chr8:96769711
|
A | G | 3 | a0001c0002t0001g0123a0003c0005t0001g0007a0009c0012t0001g0090 | 3 | HG02717.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-15153A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769711 | ||||||
| chr8:96769718
|
G | A | 2 | a0001c0002t0001g0081a0001c0002t0002g0082 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-34-15146G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769718 | ||||||
| chr8:96769735
|
A | G | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-15129A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769735 | ||||||
| chr8:96769814
|
G | T | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-34-15050G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96769814 | ||||||
| chr8:96770073
|
A | T | 2 | a0001c0002t0001g0079a0001c0002t0001g0124 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-34-14791A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770073 | ||||||
| chr8:96770130
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-14734C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770130 | ||||||
| chr8:96770394
|
G | A | 3 | a0001c0002t0001g0123a0003c0005t0001g0007a0009c0012t0001g0090 | 3 | HG02717.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-14470G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770394 | ||||||
| chr8:96770440
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-14424A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770440 | ||||||
| chr8:96770458
|
C | T | 3 | a0001c0002t0001g0123a0003c0005t0001g0007a0009c0012t0001g0090 | 3 | HG02717.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-14406C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770458 | ||||||
| chr8:96770574
|
T | C | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-14290T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770574 | ||||||
| chr8:96770594
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-14270T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770594 | ||||||
| chr8:96770726
|
A | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-34-14138A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770726 | ||||||
| chr8:96770817
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-14047T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770817 | ||||||
| chr8:96770909
|
C | T | 52 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-13955C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96770909 | ||||||
| chr8:96771081
|
TATATATA others(16): Show |
T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-13771_-34-1374 others(27): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96771081 | |||||
| chr8:96771091
|
TTA | T | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-13762_-34-1376 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96771091 | |||||
| chr8:96771097
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-13767A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771097 | ||||||
| chr8:96771102
|
T | A | 4 | a0001c0001t0001g0028a0001c0002t0001g0040a0001c0007t0001g0038others(1): Show | 4 | HG01261.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-13762T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771102 | ||||||
| chr8:96771106
|
T | A | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-13758T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771106 | ||||||
| chr8:96771273
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-13591G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771273 | ||||||
| chr8:96771496
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-13368C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771496 | ||||||
| chr8:96771686
|
C | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-13178C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771686 | ||||||
| chr8:96771781
|
T | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-34-13083T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771781 | ||||||
| chr8:96771844
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-13020T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771844 | ||||||
| chr8:96771861
|
T | C | 3 | a0001c0002t0001g0123a0003c0005t0001g0007a0009c0012t0001g0090 | 3 | HG02717.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-13003T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771861 | ||||||
| chr8:96771955
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-12909C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96771955 | ||||||
| chr8:96772136
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34-12728T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96772136 | ||||||
| chr8:96772202
|
A | C | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-12662A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96772202 | ||||||
| chr8:96772331
|
A | G | 4 | a0001c0002t0001g0123a0003c0005t0001g0007a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-12533A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96772331 | ||||||
| chr8:96772489
|
G | C | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-34-12375G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96772489 | ||||||
| chr8:96772888
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-11976G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96772888 | ||||||
| chr8:96773218
|
ATAAATAT others(15): Show |
A | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-11643_-34-1162 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96773218 | |||||
| chr8:96773314
|
A | G | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-34-11550A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96773314 | ||||||
| chr8:96773348
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-11516G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96773348 | ||||||
| chr8:96773393
|
G | A | 2 | a0002c0003t0001g0008a0002c0003t0001g0015 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34-11471G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96773393 | ||||||
| chr8:96774036
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-10828C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774036 | ||||||
| chr8:96774069
|
A | G | 4 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-10795A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774069 | ||||||
| chr8:96774127
|
C | T | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-10737C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774127 | ||||||
| chr8:96774423
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-34-10441T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774423 | ||||||
| chr8:96774495
|
T | G | 1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-34-10369T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774495 | ||||||
| chr8:96774727
|
G | A | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-34-10137G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774727 | ||||||
| chr8:96774853
|
A | T | 2 | a0001c0001t0001g0028a0001c0007t0001g0038 | 2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-10011A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774853 | ||||||
| chr8:96774940
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-9924A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96774940 | ||||||
| chr8:96775150
|
G | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-9714G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96775150 | ||||||
| chr8:96775229
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-9635T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96775229 | ||||||
| chr8:96775278
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-9586A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96775278 | ||||||
| chr8:96775487
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-9377G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96775487 | ||||||
| chr8:96775510
|
C | T | 2 | a0002c0003t0001g0087a0002c0003t0001g0089 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-34-9354C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96775510 | ||||||
| chr8:96775782
|
C | T | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-34-9082C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96775782 | ||||||
| chr8:96775849
|
C | CA | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-9014dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96775849 | |||||
| chr8:96776008
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-8856A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776008 | ||||||
| chr8:96776109
|
A | C | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-34-8755A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776109 | ||||||
| chr8:96776154
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-8710A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776154 | ||||||
| chr8:96776338
|
T | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-8526T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776338 | ||||||
| chr8:96776364
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-8500A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776364 | ||||||
| chr8:96776447
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-8417A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776447 | ||||||
| chr8:96776522
|
A | G | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-34-8342A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776522 | ||||||
| chr8:96776628
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-8236A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776628 | ||||||
| chr8:96776737
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-8127A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776737 | ||||||
| chr8:96776754
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-8110A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96776754 | ||||||
| chr8:96777468
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-34-7396G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777468 | ||||||
| chr8:96777476
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-7388A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777476 | ||||||
| chr8:96777723
|
A | AAT | 2 | a0001c0002t0001g0065a0002c0003t0001g0089 | 2 | NA19009.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-34-7104_-34-7103d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777723 | |||||
| chr8:96777723
|
A | AATAT | 4 | a0001c0002t0001g0069a0001c0002t0001g0096a0001c0002t0001g0097others(1): Show | 4 | HG01081.hp2 NA18979.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-7106_-34-7103d others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777723 | |||||
| chr8:96777723
|
A | AATATATA others(3): Show |
2 | a0001c0002t0001g0095a0003c0005t0001g0068 | 2 | HG02622.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-34-7112_-34-7103d others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777723 | |||||
| chr8:96777723
|
AAT | A | 3 | a0001c0002t0002g0050a0001c0002t0002g0085a0002c0003t0001g0052 | 3 | HG01261.hp1 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-34-7104_-34-7103d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777723 | |||||
| chr8:96777723
|
AATATAT | A | 4 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | HG03225.hp1 NA18747.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-7108_-34-7103d others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777723 | |||||
| chr8:96777742
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-34-7120_-34-7101d others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777742 | |||||
| chr8:96777742
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-34-7120_-34-7100d others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777742 | |||||
| chr8:96777742
|
ATATATAT others(16): Show |
A | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-34-7120_-34-7098d others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777742 | |||||
| chr8:96777744
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-34-7118_-34-7100d others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777744 | |||||
| chr8:96777744
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0002g0103a0001c0001t0004g0083 | 2 | HG01981.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-34-7118_-34-7099d others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777744 | |||||
| chr8:96777744
|
ATATATAT others(14): Show |
A | 28 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-34-7118_-34-7098d others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777744 | |||||
| chr8:96777744
|
ATATATAT others(15): Show |
A | 5 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0035others(2): Show | 5 | HG00733.hp1 HG01255.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-7118_-34-7097d others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777744 | |||||
| chr8:96777744
|
ATATATAT others(25): Show |
A | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004 | 3 | HG02257.hp2 HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-34-7118_-34-7087d others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777744 | |||||
| chr8:96777744
|
ATATATAT others(26): Show |
A | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-34-7118_-34-7086d others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777744 | |||||
| chr8:96777746
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0046a0001c0002t0001g0040 | 2 | HG01261.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-34-7116_-34-7098d others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777746 | |||||
| chr8:96777746
|
ATATATAT others(13): Show |
A | 3 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0002t0001g0084 | 3 | HG02970.hp2 HG03017.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-34-7116_-34-7097d others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777746 | |||||
| chr8:96777746
|
ATATATAT others(14): Show |
A | 10 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0056others(7): Show | 10 | HG01517.hp1 HG01975.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-7116_-34-7096d others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777746 | |||||
| chr8:96777746
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-7116_-34-7093d others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777746 | |||||
| chr8:96777748
|
ATATATAT others(10): Show |
A | 1 | a0003c0005t0001g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-34-7114_-34-7098d others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777748 | |||||
| chr8:96777748
|
ATATATAT others(11): Show |
A | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-34-7114_-34-7097d others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777748 | |||||
| chr8:96777750
|
ATATATAT others(21): Show |
A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-7112_-34-7085d others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777750 | |||||
| chr8:96777753
|
TATATA | T | 5 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0119others(2): Show | 5 | HG02257.hp1 HG03579.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-7110_-34-7106d others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777753 | ||||||
| chr8:96777754
|
ATATATAT others(3): Show |
A | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-34-7108_-34-7099d others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777754 | |||||
| chr8:96777754
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-34-7108_-34-7097d others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777754 | |||||
| chr8:96777755
|
TATA | T | 2 | a0001c0004t0001g0107a0002c0003t0001g0087 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-34-7108_-34-7106d others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777755 | ||||||
| chr8:96777756
|
ATATATTT others(3): Show |
A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-7106_-34-7097d others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777756 | |||||
| chr8:96777758
|
A | T | 2 | a0001c0002t0001g0094a0002c0003t0001g0052 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-34-7106A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777758 | ||||||
| chr8:96777760
|
A | ATATATAT others(11): Show |
1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-7103_-34-7102i others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777760 | |||||
| chr8:96777760
|
A | T | 11 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(8): Show | 11 | HG02257.hp1 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34-7104A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777760 | ||||||
| chr8:96777760
|
AT | A | 4 | a0001c0002t0001g0025a0001c0004t0001g0114a0002c0003t0001g0015others(1): Show | 4 | HG02004.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-7070delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777760 | |||||
| chr8:96777760
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-7083_-34-7070d others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96777760 | |||||
| chr8:96777761
|
T | TA | 4 | a0001c0002t0001g0049a0001c0002t0001g0058a0001c0002t0001g0081others(1): Show | 4 | HG02273.hp1 HG02970.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-7103_-34-7102i others(3): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777761 | ||||||
| chr8:96777761
|
T | TATATATA others(6): Show |
1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34-7103_-34-7102i others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777761 | ||||||
| chr8:96777762
|
T | A | 8 | a0001c0002t0001g0065a0001c0002t0001g0069a0001c0002t0001g0095others(5): Show | 8 | HG01081.hp2 HG01943.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-7102T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777762 | ||||||
| chr8:96777763
|
T | A | 9 | a0001c0002t0001g0049a0001c0002t0001g0058a0001c0002t0001g0081others(6): Show | 9 | HG02004.hp2 HG02273.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-7101T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777763 | ||||||
| chr8:96777764
|
T | A | 4 | a0001c0002t0001g0065a0001c0002t0001g0069a0001c0002t0002g0082others(1): Show | 4 | HG01081.hp2 HG01943.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-7100T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777764 | ||||||
| chr8:96777765
|
T | A | 3 | a0001c0002t0001g0058a0001c0002t0003g0001a0006c0010t0001g0045 | 3 | HG02004.hp2 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-34-7099T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777765 | ||||||
| chr8:96777766
|
T | A | 4 | a0001c0002t0001g0060a0001c0002t0001g0065a0001c0002t0001g0069others(1): Show | 4 | HG01081.hp2 HG02040.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-7098T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777766 | ||||||
| chr8:96777767
|
T | A | 2 | a0001c0002t0001g0058a0006c0010t0001g0045 | 2 | HG02004.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-34-7097T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777767 | ||||||
| chr8:96777768
|
T | A | 2 | a0001c0002t0001g0060a0001c0002t0001g0069 | 2 | HG01081.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-34-7096T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777768 | ||||||
| chr8:96777769
|
T | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-7095T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777769 | ||||||
| chr8:96777770
|
T | A | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-34-7094T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777770 | ||||||
| chr8:96777792
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-7072T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96777792 | ||||||
| chr8:96778280
|
A | ATTATT | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-6582_-34-6581i others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96778280 | |||||
| chr8:96778345
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-6519A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778345 | ||||||
| chr8:96778540
|
A | G | 2 | a0001c0002t0001g0121a0001c0002t0002g0039 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-34-6324A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778540 | ||||||
| chr8:96778697
|
C | T | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-6167C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778697 | ||||||
| chr8:96778882
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-34-5982T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778882 | ||||||
| chr8:96778890
|
A | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-5974A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778890 | ||||||
| chr8:96778891
|
G | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-5973G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778891 | ||||||
| chr8:96778936
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-5928G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96778936 | ||||||
| chr8:96779013
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-5851T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779013 | ||||||
| chr8:96779063
|
CA | C | 6 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0060others(3): Show | 6 | HG02040.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-5784delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96779063 | |||||
| chr8:96779077
|
A | AAAAC | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-5784_-34-5783i others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96779077 | |||||
| chr8:96779111
|
C | A | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-34-5753C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779111 | ||||||
| chr8:96779165
|
A | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-5699A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779165 | ||||||
| chr8:96779236
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-5628A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779236 | ||||||
| chr8:96779247
|
CT | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5616delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779247 | ||||||
| chr8:96779249
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5615G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779249 | ||||||
| chr8:96779253
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5611T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779253 | ||||||
| chr8:96779254
|
C | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5610C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779254 | ||||||
| chr8:96779256
|
GATGTT | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5603_-34-5599d others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96779256 | |||||
| chr8:96779259
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-5605G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779259 | ||||||
| chr8:96779350
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-5514T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779350 | ||||||
| chr8:96779386
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-34-5478G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779386 | ||||||
| chr8:96779426
|
A | G | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.-34-5438A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779426 | ||||||
| chr8:96779517
|
A | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5347A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779517 | ||||||
| chr8:96779599
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-5265T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779599 | ||||||
| chr8:96779601
|
T | A | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.-34-5263T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779601 | ||||||
| chr8:96779661
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-5203T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779661 | ||||||
| chr8:96779750
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-5114C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779750 | ||||||
| chr8:96779939
|
G | A | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-4925G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779939 | ||||||
| chr8:96779963
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-4901A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779963 | ||||||
| chr8:96779970
|
T | A | 1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-4894T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96779970 | ||||||
| chr8:96780090
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-34-4774A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96780090 | ||||||
| chr8:96780197
|
T | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-4667T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96780197 | ||||||
| chr8:96780218
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-4646A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96780218 | ||||||
| chr8:96780315
|
T | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34-4549T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96780315 | ||||||
| chr8:96780517
|
A | G | 5 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(2): Show | 5 | NA18747.hp1 NA18949.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-4347A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96780517 | ||||||
| chr8:96781103
|
C | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-3761C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96781103 | ||||||
| chr8:96781174
|
G | C | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-34-3690G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96781174 | ||||||
| chr8:96781332
|
A | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-3532A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96781332 | ||||||
| chr8:96781423
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-3441G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96781423 | ||||||
| chr8:96781606
|
G | A | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-3258G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96781606 | ||||||
| chr8:96781908
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-2956C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96781908 | ||||||
| chr8:96782024
|
G | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-2840G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782024 | ||||||
| chr8:96782064
|
T | C | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-34-2800T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782064 | ||||||
| chr8:96782361
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-2503C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782361 | ||||||
| chr8:96782380
|
C | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-34-2484C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782380 | ||||||
| chr8:96782425
|
G | A | 2 | a0001c0002t0001g0005a0001c0002t0001g0006 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-34-2439G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782425 | ||||||
| chr8:96782461
|
G | A | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-34-2403G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782461 | ||||||
| chr8:96782565
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-2299C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782565 | ||||||
| chr8:96782707
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34-2157G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782707 | ||||||
| chr8:96782784
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-2080T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782784 | ||||||
| chr8:96782903
|
A | C | 52 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-1961A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96782903 | ||||||
| chr8:96783050
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-1814C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783050 | ||||||
| chr8:96783088
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-1776T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783088 | ||||||
| chr8:96783095
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-1769C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783095 | ||||||
| chr8:96783191
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-1673G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783191 | ||||||
| chr8:96783208
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-1656A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783208 | ||||||
| chr8:96783260
|
A | AGT | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0063others(7): Show | 10 | HG00733.hp1 HG01081.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-1580_-34-1579d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96783260 | |||||
| chr8:96783260
|
A | AGTGTGTG others(9): Show |
2 | a0001c0007t0001g0038a0006c0010t0001g0045 | 2 | HG02004.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-1594_-34-1579d others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96783260 | |||||
| chr8:96783260
|
A | AGTGTGTG others(11): Show |
1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-34-1596_-34-1579d others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96783260 | |||||
| chr8:96783282
|
T | TGTGTGTG others(9): Show |
1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-1579_-34-1578i others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96783282 | |||||
| chr8:96783342
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-1522C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783342 | ||||||
| chr8:96783491
|
G | A | 52 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-1373G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783491 | ||||||
| chr8:96783637
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-1227T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783637 | ||||||
| chr8:96783739
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-34-1125C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783739 | ||||||
| chr8:96783910
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-34-954A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783910 | ||||||
| chr8:96783915
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-949A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96783915 | ||||||
| chr8:96784028
|
G | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.-34-836G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784028 | ||||||
| chr8:96784145
|
C | CTTGCATG others(8): Show |
1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-719_-34-718ins others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784145 | ||||||
| chr8:96784147
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-717C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784147 | ||||||
| chr8:96784369
|
A | G | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-34-495A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784369 | ||||||
| chr8:96784399
|
T | TG | 16 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0035others(13): Show | 16 | HG00733.hp2 HG01261.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-455dupG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 96784399 | |||||
| chr8:96784446
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-34-418G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784446 | ||||||
| chr8:96784466
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-398A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784466 | ||||||
| chr8:96784503
|
C | A | 25 | a0001c0002t0001g0018a0001c0002t0001g0071a0001c0002t0001g0072others(22): Show | 25 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-34-361C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 1/7 | chr8 | 96784503 | ||||||
| chr8:96785402
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.433+72T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96785402 | ||||||
| chr8:96785470
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+140T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96785470 | ||||||
| chr8:96785617
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+287G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96785617 | ||||||
| chr8:96785722
|
A | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.433+392A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96785722 | ||||||
| chr8:96785829
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+499C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96785829 | ||||||
| chr8:96785908
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0063others(1): Show | 4 | HG00733.hp1 HG01255.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+578G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96785908 | ||||||
| chr8:96786002
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+672T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786002 | ||||||
| chr8:96786131
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+801C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786131 | ||||||
| chr8:96786295
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+965T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786295 | ||||||
| chr8:96786491
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 15 | HG01884.hp1 HG02004.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.433+1161T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786491 | ||||||
| chr8:96786690
|
A | G | 2 | a0006c0010t0001g0045a0009c0012t0001g0090 | 2 | HG02004.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.433+1360A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786690 | ||||||
| chr8:96786757
|
A | G | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.433+1427A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786757 | ||||||
| chr8:96786800
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+1470T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96786800 | ||||||
| chr8:96787077
|
A | G | 4 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+1747A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96787077 | ||||||
| chr8:96787366
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+2036A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96787366 | ||||||
| chr8:96787525
|
C | CT | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(8): Show | 11 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.433+2225dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT | 4 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0125others(1): Show | 4 | HG02040.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+2219_433+2225d others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0031others(15): Show | 18 | HG00099.hp1 HG01081.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.433+2218_433+2225d others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT others(2): Show |
12 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0056others(9): Show | 12 | HG00099.hp2 HG00733.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.433+2217_433+2225d others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT others(3): Show |
9 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0036others(6): Show | 9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.433+2216_433+2225d others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0035a0001c0001t0002g0067 | 2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.433+2214_433+2225d others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0002g0011 | 3 | HG02809.hp2 HG02895.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.433+2213_433+2225d others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0002g0012a0001c0001t0002g0013 | 2 | HG02004.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.433+2212_433+2225d others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
CT | C | 4 | a0001c0002t0001g0006a0001c0002t0001g0120a0001c0002t0001g0123others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+2225delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.433+2216_433+2225d others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
CTTTTTTT others(5): Show |
C | 22 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(19): Show | 22 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.433+2214_433+2225d others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787525
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+2209_433+2225d others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787525 | |||||
| chr8:96787595
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+2265G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96787595 | ||||||
| chr8:96787694
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+2364G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96787694 | ||||||
| chr8:96787777
|
T | C | 1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433+2447T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96787777 | ||||||
| chr8:96787834
|
GTTGGTAT others(58): Show |
G | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.433+2506_433+2570d others(67): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787834 | |||||
| chr8:96787903
|
C | CT | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.433+2574dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96787903 | |||||
| chr8:96788000
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+2670A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96788000 | ||||||
| chr8:96788070
|
TTTTC | T | 15 | a0001c0002t0001g0018a0001c0002t0001g0071a0001c0002t0001g0072others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.433+2752_433+2755d others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96788070 | |||||
| chr8:96788163
|
C | CT | 4 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007others(1): Show | 4 | HG01261.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2845dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96788163 | |||||
| chr8:96788163
|
CT | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2845delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96788163 | |||||
| chr8:96788213
|
C | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+2883C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96788213 | ||||||
| chr8:96788648
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+3318C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96788648 | ||||||
| chr8:96788649
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+3319A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96788649 | ||||||
| chr8:96788701
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+3371T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96788701 | ||||||
| chr8:96788980
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+3650T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96788980 | ||||||
| chr8:96789170
|
T | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+3840T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789170 | ||||||
| chr8:96789370
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+4040T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789370 | ||||||
| chr8:96789574
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+4244T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789574 | ||||||
| chr8:96789630
|
T | A | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.433+4300T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789630 | ||||||
| chr8:96789670
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433+4340C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789670 | ||||||
| chr8:96789678
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+4348A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789678 | ||||||
| chr8:96789983
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+4653G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96789983 | ||||||
| chr8:96790056
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.433+4726G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96790056 | ||||||
| chr8:96790123
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+4793A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96790123 | ||||||
| chr8:96790212
|
C | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.433+4882C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96790212 | ||||||
| chr8:96790243
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+4913A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96790243 | ||||||
| chr8:96790354
|
A | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.433+5024A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96790354 | ||||||
| chr8:96790769
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+5439G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96790769 | ||||||
| chr8:96791240
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+5910A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96791240 | ||||||
| chr8:96791586
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+6256C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96791586 | ||||||
| chr8:96791685
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+6355G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96791685 | ||||||
| chr8:96791729
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+6399T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96791729 | ||||||
| chr8:96791823
|
G | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+6493G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96791823 | ||||||
| chr8:96792105
|
G | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433+6775G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792105 | ||||||
| chr8:96792177
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.433+6847A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792177 | ||||||
| chr8:96792190
|
C | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+6860C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792190 | ||||||
| chr8:96792319
|
T | C | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.433+6989T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792319 | ||||||
| chr8:96792370
|
C | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.433+7040C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792370 | ||||||
| chr8:96792462
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+7132T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792462 | ||||||
| chr8:96792482
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+7152C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792482 | ||||||
| chr8:96792602
|
G | A | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.433+7272G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792602 | ||||||
| chr8:96792807
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+7477A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792807 | ||||||
| chr8:96792908
|
G | A | 3 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045 | 3 | HG02004.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.433+7578G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792908 | ||||||
| chr8:96792913
|
A | G | 120 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.433+7583A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96792913 | ||||||
| chr8:96793032
|
GC | G | 4 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+7708delC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96793032 | |||||
| chr8:96793222
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+7892C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793222 | ||||||
| chr8:96793544
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+8214T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793544 | ||||||
| chr8:96793641
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+8311A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793641 | ||||||
| chr8:96793674
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+8344C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793674 | ||||||
| chr8:96793698
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+8368C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793698 | ||||||
| chr8:96793851
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+8521A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793851 | ||||||
| chr8:96793881
|
C | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.433+8551C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793881 | ||||||
| chr8:96793944
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+8614T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793944 | ||||||
| chr8:96793951
|
G | A | 1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.433+8621G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96793951 | ||||||
| chr8:96794026
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+8696G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794026 | ||||||
| chr8:96794206
|
A | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.433+8876A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794206 | ||||||
| chr8:96794345
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.433+9015C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794345 | ||||||
| chr8:96794346
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+9016G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794346 | ||||||
| chr8:96794353
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+9023A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794353 | ||||||
| chr8:96794370
|
C | G | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.433+9040C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794370 | ||||||
| chr8:96794420
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+9090T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794420 | ||||||
| chr8:96794662
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433+9332C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794662 | ||||||
| chr8:96794782
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+9452A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794782 | ||||||
| chr8:96794811
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.433+9481G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794811 | ||||||
| chr8:96794844
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+9514C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794844 | ||||||
| chr8:96794876
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+9546A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96794876 | ||||||
| chr8:96795177
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+9847A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96795177 | ||||||
| chr8:96795187
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.433+9857A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96795187 | ||||||
| chr8:96795405
|
A | G | 1 | a0001c0002t0001g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.433+10075A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96795405 | ||||||
| chr8:96795634
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+10304T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96795634 | ||||||
| chr8:96795716
|
AT | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+10393delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96795716 | |||||
| chr8:96795832
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+10502T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96795832 | ||||||
| chr8:96796169
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+10839T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796169 | ||||||
| chr8:96796255
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+10925A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796255 | ||||||
| chr8:96796311
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.433+10981G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796311 | ||||||
| chr8:96796312
|
C | T | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.433+10982C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796312 | ||||||
| chr8:96796318
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+10988T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796318 | ||||||
| chr8:96796336
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.433+11006T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796336 | ||||||
| chr8:96796661
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+11331A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796661 | ||||||
| chr8:96796897
|
G | C | 4 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+11567G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96796897 | ||||||
| chr8:96797220
|
G | C | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.433+11890G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797220 | ||||||
| chr8:96797281
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+11951G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797281 | ||||||
| chr8:96797417
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+12087A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797417 | ||||||
| chr8:96797470
|
G | A | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.433+12140G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797470 | ||||||
| chr8:96797494
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+12164G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797494 | ||||||
| chr8:96797512
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+12182T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797512 | ||||||
| chr8:96797725
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0024 | 3 | HG02630.hp1 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.433+12395C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797725 | ||||||
| chr8:96797817
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+12487C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797817 | ||||||
| chr8:96797877
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+12547C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797877 | ||||||
| chr8:96797914
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+12584T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797914 | ||||||
| chr8:96797918
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+12588G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96797918 | ||||||
| chr8:96798050
|
C | CA | 7 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.433+12733dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96798050 | |||||
| chr8:96798329
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+12999T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798329 | ||||||
| chr8:96798333
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.433+13003A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798333 | ||||||
| chr8:96798457
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+13127A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798457 | ||||||
| chr8:96798530
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+13200G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798530 | ||||||
| chr8:96798542
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+13212T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798542 | ||||||
| chr8:96798961
|
A | G | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.433+13631A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798961 | ||||||
| chr8:96798972
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+13642A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798972 | ||||||
| chr8:96798988
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.433+13658A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96798988 | ||||||
| chr8:96799005
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+13675T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96799005 | ||||||
| chr8:96799038
|
T | C | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.433+13708T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96799038 | ||||||
| chr8:96799442
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+14112A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96799442 | ||||||
| chr8:96799596
|
G | A | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433+14266G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96799596 | ||||||
| chr8:96799865
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+14535A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96799865 | ||||||
| chr8:96800023
|
G | A | 2 | a0002c0003t0001g0087a0002c0003t0001g0089 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.433+14693G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96800023 | ||||||
| chr8:96800602
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+15272G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96800602 | ||||||
| chr8:96800976
|
A | AT | 63 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.433+15663dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96800976 | |||||
| chr8:96800976
|
AT | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0002t0001g0092others(2): Show | 5 | HG02717.hp2 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+15663delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96800976 | |||||
| chr8:96801132
|
C | T | 5 | a0001c0001t0001g0028a0001c0002t0001g0058a0001c0007t0001g0038others(2): Show | 5 | HG02004.hp2 HG02965.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+15802C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96801132 | ||||||
| chr8:96801257
|
G | T | 6 | a0001c0002t0001g0018a0001c0002t0001g0073a0001c0002t0001g0113others(3): Show | 6 | HG02055.hp2 NA18522.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.433+15927G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96801257 | ||||||
| chr8:96801262
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+15932C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96801262 | ||||||
| chr8:96801365
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.433+16035T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96801365 | ||||||
| chr8:96801381
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+16051T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96801381 | ||||||
| chr8:96801711
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.433+16381G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96801711 | ||||||
| chr8:96801782
|
ACCTCCTC others(4): Show |
A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+16467_433+1647 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96801782 | |||||
| chr8:96802136
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+16806G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802136 | ||||||
| chr8:96802257
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.433+16927T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802257 | ||||||
| chr8:96802260
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+16930G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802260 | ||||||
| chr8:96802268
|
A | G | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.433+16938A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802268 | ||||||
| chr8:96802309
|
A | T | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.433+16979A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802309 | ||||||
| chr8:96802321
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+16991G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802321 | ||||||
| chr8:96802390
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.433+17060T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802390 | ||||||
| chr8:96802556
|
T | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG00733.hp2 HG01261.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.433+17226T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802556 | ||||||
| chr8:96802574
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+17244G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802574 | ||||||
| chr8:96802637
|
A | G | 54 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.433+17307A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802637 | ||||||
| chr8:96802726
|
T | A | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.433+17396T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802726 | ||||||
| chr8:96802983
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.433+17653A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96802983 | ||||||
| chr8:96802990
|
T | TAC | 25 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0023others(22): Show | 25 | HG01884.hp1 HG01943.hp2 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.433+17690_433+1769 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96802990 | |||||
| chr8:96802990
|
T | TACAC | 5 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0011others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.433+17688_433+1769 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96802990 | |||||
| chr8:96802990
|
TAC | T | 3 | a0001c0002t0001g0122a0001c0002t0002g0004a0006c0010t0001g0045 | 3 | HG02004.hp2 HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.433+17690_433+1769 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96802990 | |||||
| chr8:96802990
|
TACAC | T | 4 | a0001c0002t0001g0040a0001c0002t0001g0123a0001c0007t0001g0038others(1): Show | 4 | HG01261.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+17688_433+1769 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96802990 | |||||
| chr8:96803668
|
G | GATATCCC others(12): Show |
3 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045 | 3 | HG02004.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.433+18339_433+1834 others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96803668 | |||||
| chr8:96803702
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+18372C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96803702 | ||||||
| chr8:96803967
|
A | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433+18637A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96803967 | ||||||
| chr8:96804077
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.433+18747G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804077 | ||||||
| chr8:96804092
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+18762A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804092 | ||||||
| chr8:96804191
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+18861A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804191 | ||||||
| chr8:96804583
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19253T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804583 | ||||||
| chr8:96804601
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.433+19271A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804601 | ||||||
| chr8:96804639
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+19309A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804639 | ||||||
| chr8:96804686
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19356A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804686 | ||||||
| chr8:96804909
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19579T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96804909 | ||||||
| chr8:96805067
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19737T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805067 | ||||||
| chr8:96805073
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+19743T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805073 | ||||||
| chr8:96805129
|
A | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19799A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805129 | ||||||
| chr8:96805149
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19819G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805149 | ||||||
| chr8:96805173
|
C | G | 4 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045others(1): Show | 4 | HG02004.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+19843C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805173 | ||||||
| chr8:96805259
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+19929T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805259 | ||||||
| chr8:96805411
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.433+20081C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805411 | ||||||
| chr8:96805427
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433+20097C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805427 | ||||||
| chr8:96805428
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+20098G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805428 | ||||||
| chr8:96805437
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.433+20107A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805437 | ||||||
| chr8:96805462
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+20132A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805462 | ||||||
| chr8:96805729
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.433+20399C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805729 | ||||||
| chr8:96805819
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.433+20489G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96805819 | ||||||
| chr8:96806158
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+20828T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806158 | ||||||
| chr8:96806229
|
C | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+20899C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806229 | ||||||
| chr8:96806243
|
T | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433+20913T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806243 | ||||||
| chr8:96806265
|
AAAATT | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+20936_433+2094 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806265 | ||||||
| chr8:96806292
|
A | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+20962A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806292 | ||||||
| chr8:96806301
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+20971C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806301 | ||||||
| chr8:96806381
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.433+21051G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806381 | ||||||
| chr8:96806515
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+21185A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806515 | ||||||
| chr8:96806970
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+21640A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96806970 | ||||||
| chr8:96807179
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.433+21849G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807179 | ||||||
| chr8:96807222
|
G | GT | 30 | a0001c0002t0001g0018a0001c0002t0001g0071a0001c0002t0001g0072others(27): Show | 30 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.433+21902dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96807222 | |||||
| chr8:96807484
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+22154G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807484 | ||||||
| chr8:96807493
|
A | G | 21 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(18): Show | 21 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.433+22163A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807493 | ||||||
| chr8:96807592
|
A | G | 4 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0069others(1): Show | 4 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+22262A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807592 | ||||||
| chr8:96807609
|
T | C | 1 | a0001c0002t0001g0065 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.433+22279T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807609 | ||||||
| chr8:96807710
|
T | C | 1 | a0001c0002t0002g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433+22380T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807710 | ||||||
| chr8:96807720
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+22390T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807720 | ||||||
| chr8:96807966
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+22636G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96807966 | ||||||
| chr8:96808151
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+22821G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96808151 | ||||||
| chr8:96808538
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.433+23208T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96808538 | ||||||
| chr8:96808587
|
G | A | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.433+23257G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96808587 | ||||||
| chr8:96808822
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.433+23492C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96808822 | ||||||
| chr8:96809143
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433+23813G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96809143 | ||||||
| chr8:96809384
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.433+24054A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96809384 | ||||||
| chr8:96809682
|
T | A | 3 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045 | 3 | HG02004.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.433+24352T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96809682 | ||||||
| chr8:96809932
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.433+24602C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96809932 | ||||||
| chr8:96809934
|
C | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(5): Show | 8 | HG00099.hp2 HG01255.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.433+24604C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96809934 | ||||||
| chr8:96810026
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.433+24696A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810026 | ||||||
| chr8:96810501
|
G | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0123a0003c0005t0001g0007 | 3 | HG01261.hp2 HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-24472G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810501 | ||||||
| chr8:96810547
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.434-24426G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810547 | ||||||
| chr8:96810550
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-24423G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810550 | ||||||
| chr8:96810571
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.434-24402T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810571 | ||||||
| chr8:96810884
|
A | G | 53 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.434-24089A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810884 | ||||||
| chr8:96810897
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.434-24076G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96810897 | ||||||
| chr8:96811245
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.434-23728C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96811245 | ||||||
| chr8:96811255
|
TA | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-23711delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96811255 | |||||
| chr8:96811731
|
C | T | 3 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045 | 3 | HG02004.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.434-23242C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96811731 | ||||||
| chr8:96811863
|
C | T | 3 | a0001c0001t0001g0028a0001c0007t0001g0038a0006c0010t0001g0045 | 3 | HG02004.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.434-23110C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96811863 | ||||||
| chr8:96811870
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.434-23103C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96811870 | ||||||
| chr8:96811890
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-23083C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96811890 | ||||||
| chr8:96812327
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-22646T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96812327 | ||||||
| chr8:96812438
|
G | A | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-22535G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96812438 | ||||||
| chr8:96812690
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0110 | 2 | HG03516.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.434-22283G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96812690 | ||||||
| chr8:96812899
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.434-22074A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96812899 | ||||||
| chr8:96812980
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.434-21993C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96812980 | ||||||
| chr8:96813010
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-21963G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813010 | ||||||
| chr8:96813022
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103 | 3 | HG01975.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.434-21951A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813022 | ||||||
| chr8:96813189
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-21784C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813189 | ||||||
| chr8:96813245
|
T | C | 2 | a0002c0003t0001g0087a0002c0003t0001g0089 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.434-21728T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813245 | ||||||
| chr8:96813306
|
G | C | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.434-21667G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813306 | ||||||
| chr8:96813794
|
T | TA | 3 | a0001c0001t0001g0028a0001c0001t0001g0110a0009c0012t0001g0090 | 3 | HG02965.hp2 HG03516.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.434-21178dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96813794 | |||||
| chr8:96813854
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-21119C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813854 | ||||||
| chr8:96813878
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0002t0001g0040others(2): Show | 5 | HG01261.hp2 HG02004.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-21095T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813878 | ||||||
| chr8:96813903
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-21070A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96813903 | ||||||
| chr8:96814001
|
C | CACAT | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.434-20970_434-2096 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96814001 | |||||
| chr8:96814056
|
G | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.434-20917G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814056 | ||||||
| chr8:96814221
|
G | A | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-20752G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814221 | ||||||
| chr8:96814277
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.434-20696A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814277 | ||||||
| chr8:96814430
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0102others(2): Show | 5 | HG01255.hp2 HG03017.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.434-20543A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814430 | ||||||
| chr8:96814515
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434-20458T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814515 | ||||||
| chr8:96814543
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.434-20430A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814543 | ||||||
| chr8:96814654
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434-20319G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814654 | ||||||
| chr8:96814742
|
C | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-20231C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814742 | ||||||
| chr8:96814784
|
T | C | 1 | a0003c0005t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.434-20189T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814784 | ||||||
| chr8:96814842
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434-20131A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96814842 | ||||||
| chr8:96815032
|
G | A | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.434-19941G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96815032 | ||||||
| chr8:96815478
|
A | T | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-19495A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96815478 | ||||||
| chr8:96816118
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.434-18855G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96816118 | ||||||
| chr8:96816311
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-18662A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96816311 | ||||||
| chr8:96816571
|
G | T | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.434-18402G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96816571 | ||||||
| chr8:96816927
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-18046T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96816927 | ||||||
| chr8:96816976
|
C | T | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-17997C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96816976 | ||||||
| chr8:96817156
|
G | T | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-17817G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817156 | ||||||
| chr8:96817162
|
C | T | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.434-17811C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817162 | ||||||
| chr8:96817192
|
G | C | 1 | a0001c0002t0001g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.434-17781G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817192 | ||||||
| chr8:96817427
|
T | G | 1 | a0001c0001t0002g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.434-17546T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817427 | ||||||
| chr8:96817569
|
A | T | 1 | a0001c0002t0003g0001 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.434-17404A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817569 | ||||||
| chr8:96817594
|
G | A | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.434-17379G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817594 | ||||||
| chr8:96817623
|
T | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-17350T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817623 | ||||||
| chr8:96817689
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.434-17284C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817689 | ||||||
| chr8:96817807
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.434-17166G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96817807 | ||||||
| chr8:96818317
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.434-16656C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818317 | ||||||
| chr8:96818318
|
G | A | 1 | a0003c0005t0001g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.434-16655G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818318 | ||||||
| chr8:96818346
|
A | G | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-16627A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818346 | ||||||
| chr8:96818350
|
C | T | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.434-16623C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818350 | ||||||
| chr8:96818435
|
A | G | 3 | a0001c0002t0001g0120a0001c0002t0002g0039a0001c0008t0001g0116 | 3 | HG02109.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.434-16538A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818435 | ||||||
| chr8:96818484
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.434-16489C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818484 | ||||||
| chr8:96818872
|
T | C | 6 | a0001c0002t0001g0086a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | NA18979.hp1 NA18990.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.434-16101T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96818872 | ||||||
| chr8:96819086
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434-15887T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96819086 | ||||||
| chr8:96819212
|
GGA | G | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.434-15759_434-1575 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96819212 | |||||
| chr8:96820224
|
T | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-14749T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96820224 | ||||||
| chr8:96820515
|
T | C | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.434-14458T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96820515 | ||||||
| chr8:96820691
|
G | A | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.434-14282G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96820691 | ||||||
| chr8:96820939
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-14034G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96820939 | ||||||
| chr8:96820978
|
T | C | 66 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.434-13995T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96820978 | ||||||
| chr8:96821091
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.434-13882G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821091 | ||||||
| chr8:96821126
|
AT | A | 49 | a0001c0001t0001g0028a0001c0001t0001g0076a0001c0001t0002g0020others(46): Show | 49 | HG01081.hp2 HG01516.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.434-13822delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96821126 | |||||
| chr8:96821126
|
ATT | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.434-13823_434-1382 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96821126 | |||||
| chr8:96821260
|
G | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.434-13713G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821260 | ||||||
| chr8:96821264
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-13709G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821264 | ||||||
| chr8:96821524
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.434-13449T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821524 | ||||||
| chr8:96821708
|
T | C | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.434-13265T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821708 | ||||||
| chr8:96821751
|
T | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-13222T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821751 | ||||||
| chr8:96821810
|
A | C | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-13163A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821810 | ||||||
| chr8:96821871
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.434-13102A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96821871 | ||||||
| chr8:96822405
|
T | C | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.434-12568T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96822405 | ||||||
| chr8:96822449
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434-12524G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96822449 | ||||||
| chr8:96822806
|
G | A | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-12167G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96822806 | ||||||
| chr8:96822954
|
C | A | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.434-12019C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96822954 | ||||||
| chr8:96823512
|
CA | C | 5 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-11458delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96823512 | |||||
| chr8:96823688
|
TATAA | T | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-11275_434-1127 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96823688 | |||||
| chr8:96824005
|
T | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-10968T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824005 | ||||||
| chr8:96824117
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.434-10856T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824117 | ||||||
| chr8:96824172
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.434-10801C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824172 | ||||||
| chr8:96824211
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.434-10762G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824211 | ||||||
| chr8:96824349
|
A | G | 1 | a0004c0006t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.434-10624A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824349 | ||||||
| chr8:96824624
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.434-10349A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824624 | ||||||
| chr8:96824910
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-10063G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96824910 | ||||||
| chr8:96825004
|
G | A | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.434-9969G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96825004 | ||||||
| chr8:96825341
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-9632G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96825341 | ||||||
| chr8:96825419
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.434-9554A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96825419 | ||||||
| chr8:96825582
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.434-9391A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96825582 | ||||||
| chr8:96825965
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-9008A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96825965 | ||||||
| chr8:96826180
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.434-8793A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826180 | ||||||
| chr8:96826471
|
G | GTA | 4 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | NA18747.hp1 NA18962.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-8491_434-8490d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96826471 | |||||
| chr8:96826629
|
A | T | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.434-8344A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826629 | ||||||
| chr8:96826790
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-8183C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826790 | ||||||
| chr8:96826807
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434-8166G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826807 | ||||||
| chr8:96826853
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-8120C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826853 | ||||||
| chr8:96826929
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.434-8044T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826929 | ||||||
| chr8:96826991
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.434-7982G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96826991 | ||||||
| chr8:96827001
|
T | C | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.434-7972T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96827001 | ||||||
| chr8:96827151
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-7822G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96827151 | ||||||
| chr8:96827361
|
G | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-7612G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96827361 | ||||||
| chr8:96827509
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.434-7464C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96827509 | ||||||
| chr8:96827804
|
A | G | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.434-7169A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96827804 | ||||||
| chr8:96827999
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.434-6974T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96827999 | ||||||
| chr8:96828126
|
T | G | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434-6847T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96828126 | ||||||
| chr8:96828438
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-6535A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96828438 | ||||||
| chr8:96828842
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.434-6131G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96828842 | ||||||
| chr8:96828849
|
A | G | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-6124A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96828849 | ||||||
| chr8:96828935
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-6038C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96828935 | ||||||
| chr8:96829039
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-5934G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96829039 | ||||||
| chr8:96829264
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.434-5709C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96829264 | ||||||
| chr8:96829266
|
C | G | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.434-5707C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96829266 | ||||||
| chr8:96829480
|
G | C | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.434-5493G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96829480 | ||||||
| chr8:96829713
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-5260T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96829713 | ||||||
| chr8:96829941
|
T | G | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.434-5032T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96829941 | ||||||
| chr8:96830144
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.434-4829G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96830144 | ||||||
| chr8:96830261
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-4712A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96830261 | ||||||
| chr8:96830278
|
G | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.434-4695G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96830278 | ||||||
| chr8:96830494
|
T | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434-4479T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96830494 | ||||||
| chr8:96830865
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434-4108G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96830865 | ||||||
| chr8:96830866
|
C | A | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.434-4107C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96830866 | ||||||
| chr8:96831176
|
G | A | 50 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.434-3797G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96831176 | ||||||
| chr8:96831196
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-3777C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96831196 | ||||||
| chr8:96831230
|
A | ATG | 3 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0004t0001g0107 | 3 | HG03516.hp1 HG03927.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.434-3723_434-3722d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96831230 | |||||
| chr8:96831242
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.434-3731G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96831242 | ||||||
| chr8:96831294
|
T | G | 49 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.434-3679T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96831294 | ||||||
| chr8:96831554
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-3419G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96831554 | ||||||
| chr8:96831607
|
G | A | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.434-3366G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96831607 | ||||||
| chr8:96832162
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-2811T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96832162 | ||||||
| chr8:96832433
|
T | C | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.434-2540T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96832433 | ||||||
| chr8:96832456
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434-2517T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96832456 | ||||||
| chr8:96832734
|
G | T | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-2239G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96832734 | ||||||
| chr8:96833086
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1887A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833086 | ||||||
| chr8:96833321
|
A | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.434-1652A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833321 | ||||||
| chr8:96833349
|
A | G | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.434-1624A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833349 | ||||||
| chr8:96833436
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-1537C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833436 | ||||||
| chr8:96833453
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434-1520C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833453 | ||||||
| chr8:96833470
|
C | G | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434-1503C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833470 | ||||||
| chr8:96833577
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.434-1396A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833577 | ||||||
| chr8:96833982
|
T | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.434-991T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96833982 | ||||||
| chr8:96834241
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.434-732A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96834241 | ||||||
| chr8:96834348
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.434-625G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | chr8 | 96834348 | ||||||
| chr8:96834536
|
GGTT | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.434-433_434-431del others(3): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 96834536 | |||||
| chr8:96835304
|
C | A | 1 | a0001c0002t0002g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.641+124C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96835304 | ||||||
| chr8:96835304
|
C | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+124C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96835304 | ||||||
| chr8:96835380
|
C | T | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.641+200C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96835380 | ||||||
| chr8:96835546
|
C | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.641+366C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96835546 | ||||||
| chr8:96835635
|
A | C | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.641+455A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96835635 | ||||||
| chr8:96835761
|
A | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103 | 3 | HG01975.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.641+581A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96835761 | ||||||
| chr8:96836019
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.641+839G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836019 | ||||||
| chr8:96836145
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+965G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836145 | ||||||
| chr8:96836150
|
C | T | 7 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+970C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836150 | ||||||
| chr8:96836430
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.641+1250C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836430 | ||||||
| chr8:96836516
|
C | G | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.641+1336C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836516 | ||||||
| chr8:96836585
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+1405A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836585 | ||||||
| chr8:96836793
|
A | AT | 5 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0112others(2): Show | 5 | HG03516.hp1 HG03927.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+1628dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96836793 | |||||
| chr8:96836801
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.641+1621T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836801 | ||||||
| chr8:96836952
|
C | A | 1 | a0001c0002t0001g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.641+1772C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96836952 | ||||||
| chr8:96837004
|
T | G | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.641+1824T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837004 | ||||||
| chr8:96837172
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.641+1992A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837172 | ||||||
| chr8:96837178
|
TAAA | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | NA18747.hp1 NA18962.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+2001_641+2003d others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96837178 | |||||
| chr8:96837235
|
T | C | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.641+2055T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837235 | ||||||
| chr8:96837286
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+2106A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837286 | ||||||
| chr8:96837500
|
T | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.641+2320T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837500 | ||||||
| chr8:96837579
|
A | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+2399A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837579 | ||||||
| chr8:96837604
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.641+2424A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837604 | ||||||
| chr8:96837865
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.641+2685T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96837865 | ||||||
| chr8:96838204
|
T | G | 8 | a0002c0003t0001g0008a0002c0003t0001g0015a0002c0003t0001g0052others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+3024T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96838204 | ||||||
| chr8:96838784
|
C | G | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.641+3604C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96838784 | ||||||
| chr8:96838825
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+3645G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96838825 | ||||||
| chr8:96839057
|
ATAT | A | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.641+3881_641+3883d others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96839057 | |||||
| chr8:96839093
|
TTA | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.641+3931_641+3932d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96839093 | |||||
| chr8:96839311
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.641+4131T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96839311 | ||||||
| chr8:96839350
|
T | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.641+4170T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96839350 | ||||||
| chr8:96839609
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.641+4429A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96839609 | ||||||
| chr8:96839679
|
G | A | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.641+4499G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96839679 | ||||||
| chr8:96839951
|
T | A | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.641+4771T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96839951 | ||||||
| chr8:96840000
|
C | CAG | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.641+4821_641+4822d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96840000 | |||||
| chr8:96840062
|
A | G | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.641+4882A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96840062 | ||||||
| chr8:96840696
|
A | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+5516A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96840696 | ||||||
| chr8:96840866
|
T | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.641+5686T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96840866 | ||||||
| chr8:96840968
|
G | A | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.641+5788G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96840968 | ||||||
| chr8:96840979
|
C | A | 1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.641+5799C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96840979 | ||||||
| chr8:96841064
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.641+5884C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841064 | ||||||
| chr8:96841145
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.641+5965C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841145 | ||||||
| chr8:96841281
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.641+6101C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841281 | ||||||
| chr8:96841289
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+6109C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841289 | ||||||
| chr8:96841372
|
A | G | 2 | a0001c0002t0001g0123a0003c0005t0001g0007 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.641+6192A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841372 | ||||||
| chr8:96841538
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+6358C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841538 | ||||||
| chr8:96841677
|
G | A | 49 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.641+6497G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841677 | ||||||
| chr8:96841885
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.641+6705T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96841885 | ||||||
| chr8:96842275
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+7095A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96842275 | ||||||
| chr8:96842310
|
A | G | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.641+7130A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96842310 | ||||||
| chr8:96842470
|
G | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+7290G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96842470 | ||||||
| chr8:96842510
|
A | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+7330A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96842510 | ||||||
| chr8:96842518
|
G | GGA | 101 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.641+7339_641+7340i others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96842518 | |||||
| chr8:96842846
|
G | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+7666G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96842846 | ||||||
| chr8:96842979
|
A | C | 51 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0035others(48): Show | 51 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.641+7799A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96842979 | ||||||
| chr8:96843313
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(15): Show | 18 | HG00733.hp2 HG02004.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.641+8133C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96843313 | ||||||
| chr8:96843649
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.641+8469T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96843649 | ||||||
| chr8:96844041
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0002g0044 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641+8861T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844041 | ||||||
| chr8:96844080
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.641+8900C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844080 | ||||||
| chr8:96844606
|
C | T | 36 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(33): Show | 36 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.641+9426C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844606 | ||||||
| chr8:96844693
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+9513T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844693 | ||||||
| chr8:96844709
|
C | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+9529C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844709 | ||||||
| chr8:96844780
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+9600A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844780 | ||||||
| chr8:96844865
|
A | G | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.641+9685A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96844865 | ||||||
| chr8:96845306
|
A | G | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.641+10126A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96845306 | ||||||
| chr8:96845769
|
G | GGCC | 4 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(1): Show | 4 | HG02630.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+10590_641+1059 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96845769 | |||||
| chr8:96845898
|
C | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.641+10718C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96845898 | ||||||
| chr8:96846088
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.641+10908G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96846088 | ||||||
| chr8:96846332
|
T | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.641+11152T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96846332 | ||||||
| chr8:96846543
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+11363C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96846543 | ||||||
| chr8:96846728
|
G | A | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.641+11548G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96846728 | ||||||
| chr8:96847046
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.641+11866A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847046 | ||||||
| chr8:96847151
|
C | T | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(51): Show | 54 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.641+11971C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847151 | ||||||
| chr8:96847172
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+11992T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847172 | ||||||
| chr8:96847302
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+12122C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847302 | ||||||
| chr8:96847519
|
T | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.641+12339T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847519 | ||||||
| chr8:96847836
|
CT | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(6): Show | 9 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.641+12674delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96847836 | |||||
| chr8:96847893
|
C | CT | 4 | a0001c0001t0002g0044a0001c0002t0001g0084a0001c0002t0002g0039others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+12733dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96847893 | |||||
| chr8:96847893
|
CT | C | 6 | a0001c0001t0001g0108a0001c0002t0001g0071a0001c0002t0001g0072others(3): Show | 6 | HG02040.hp2 NA18747.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.641+12733delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96847893 | |||||
| chr8:96847893
|
CTT | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(33): Show | 36 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.641+12732_641+1273 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96847893 | |||||
| chr8:96847909
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.641+12729T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847909 | ||||||
| chr8:96847955
|
G | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(58): Show | 61 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.641+12775G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847955 | ||||||
| chr8:96847956
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.641+12776C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96847956 | ||||||
| chr8:96848018
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.641+12838T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848018 | ||||||
| chr8:96848293
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+13113G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848293 | ||||||
| chr8:96848327
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.641+13147A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848327 | ||||||
| chr8:96848328
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.641+13148C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848328 | ||||||
| chr8:96848418
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.641+13238G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848418 | ||||||
| chr8:96848759
|
A | T | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.641+13579A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848759 | ||||||
| chr8:96848941
|
A | G | 10 | a0002c0003t0001g0008a0002c0003t0001g0015a0002c0003t0001g0052others(7): Show | 10 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.641+13761A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848941 | ||||||
| chr8:96848978
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.641+13798T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96848978 | ||||||
| chr8:96849064
|
TTTTAACA others(9): Show |
T | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.641+13885_641+1390 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96849064 | ||||||
| chr8:96849097
|
A | G | 42 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(39): Show | 42 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.641+13917A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96849097 | ||||||
| chr8:96849299
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+14119C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96849299 | ||||||
| chr8:96850537
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+15357G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96850537 | ||||||
| chr8:96850565
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+15385T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96850565 | ||||||
| chr8:96850584
|
T | TTTTA | 38 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(35): Show | 38 | HG00099.hp2 HG00733.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.641+15443_641+1544 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96850584 | |||||
| chr8:96850584
|
T | TTTTATTT others(1): Show |
9 | a0001c0001t0001g0009a0001c0002t0001g0058a0001c0002t0001g0065others(6): Show | 9 | HG01884.hp2 HG02809.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.641+15439_641+1544 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96850584 | |||||
| chr8:96850584
|
T | TTTTATTT others(6): Show |
1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+15411_641+1541 others(17): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96850584 | |||||
| chr8:96850584
|
TTTTA | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0076a0001c0002t0001g0018others(4): Show | 7 | HG00099.hp1 HG02004.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.641+15443_641+1544 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96850584 | |||||
| chr8:96850584
|
TTTTATTT others(1): Show |
T | 3 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0069 | 3 | HG01081.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.641+15439_641+1544 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96850584 | |||||
| chr8:96850592
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.641+15412A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96850592 | ||||||
| chr8:96850694
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+15514C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96850694 | ||||||
| chr8:96850712
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0002g0011a0001c0001t0002g0013 | 3 | HG02809.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.641+15532C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96850712 | ||||||
| chr8:96850898
|
C | G | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.641+15718C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96850898 | ||||||
| chr8:96851034
|
T | A | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(57): Show | 60 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.641+15854T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851034 | ||||||
| chr8:96851091
|
AT | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.641+15912delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851091 | ||||||
| chr8:96851362
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+16182A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851362 | ||||||
| chr8:96851532
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+16352A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851532 | ||||||
| chr8:96851621
|
A | T | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.641+16441A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851621 | ||||||
| chr8:96851705
|
G | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+16525G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851705 | ||||||
| chr8:96851810
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(52): Show | 55 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.641+16630C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96851810 | ||||||
| chr8:96852141
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+16961C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96852141 | ||||||
| chr8:96852315
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+17135C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96852315 | ||||||
| chr8:96852343
|
A | C | 67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(64): Show | 67 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.641+17163A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96852343 | ||||||
| chr8:96852395
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+17215C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96852395 | ||||||
| chr8:96852532
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+17352C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96852532 | ||||||
| chr8:96852845
|
G | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.641+17665G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96852845 | ||||||
| chr8:96853177
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.641+17997G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853177 | ||||||
| chr8:96853201
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+18021C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853201 | ||||||
| chr8:96853248
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.641+18068T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853248 | ||||||
| chr8:96853255
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+18075C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853255 | ||||||
| chr8:96853262
|
G | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.641+18082G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853262 | ||||||
| chr8:96853282
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+18102G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853282 | ||||||
| chr8:96853341
|
A | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.641+18161A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853341 | ||||||
| chr8:96853517
|
T | C | 1 | a0001c0002t0001g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.641+18337T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853517 | ||||||
| chr8:96853563
|
AT | A | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.641+18397delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96853563 | |||||
| chr8:96853872
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+18692C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853872 | ||||||
| chr8:96853927
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.641+18747G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853927 | ||||||
| chr8:96853952
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+18772T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96853952 | ||||||
| chr8:96854007
|
C | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.641+18827C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854007 | ||||||
| chr8:96854059
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.641+18879G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854059 | ||||||
| chr8:96854257
|
C | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.641+19077C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854257 | ||||||
| chr8:96854338
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.641+19158C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854338 | ||||||
| chr8:96854387
|
A | C | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.641+19207A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854387 | ||||||
| chr8:96854394
|
A | G | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+19214A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854394 | ||||||
| chr8:96854485
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.641+19305T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854485 | ||||||
| chr8:96854486
|
G | C | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.641+19306G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854486 | ||||||
| chr8:96854510
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+19330G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854510 | ||||||
| chr8:96854518
|
G | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.641+19338G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854518 | ||||||
| chr8:96854530
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0001g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.641+19369_641+1937 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0031a0001c0002t0001g0066 | 2 | NA18945.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.641+19368_641+1937 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(10): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(5): Show | 8 | HG01517.hp1 HG01884.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+19363_641+1937 others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(11): Show |
11 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0036others(8): Show | 11 | HG01261.hp1 HG01261.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.641+19362_641+1937 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0002g0013a0001c0002t0001g0084a0001c0002t0002g0085others(1): Show | 4 | HG02970.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+19361_641+1937 others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0078a0001c0001t0001g0109a0001c0001t0002g0024others(1): Show | 4 | HG02630.hp1 NA18949.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+19360_641+1937 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(14): Show |
4 | a0001c0001t0001g0032a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | HG01516.hp1 HG01517.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+19359_641+1937 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0070a0001c0001t0002g0022others(1): Show | 4 | HG02572.hp1 HG04184.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+19358_641+1937 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(16): Show |
6 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0002g0029others(3): Show | 6 | HG01081.hp1 HG01981.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.641+19357_641+1937 others(27): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(17): Show |
2 | a0001c0002t0001g0060a0001c0002t0001g0106 | 2 | HG02040.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.641+19356_641+1937 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(18): Show |
2 | a0001c0002t0001g0069a0001c0002t0001g0095 | 2 | HG01081.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.641+19355_641+1937 others(29): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.641+19354_641+1937 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854530
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0104 | 2 | HG01255.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.641+19351_641+1937 others(33): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854530 | |||||
| chr8:96854547
|
A | ACAAAAC | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.641+19367_641+1936 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854547 | ||||||
| chr8:96854549
|
A | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.641+19369A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854549 | ||||||
| chr8:96854550
|
A | C | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.641+19370A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854550 | ||||||
| chr8:96854555
|
A | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+19375A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854555 | ||||||
| chr8:96854557
|
A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.641+19379_641+1938 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854557 | |||||
| chr8:96854557
|
A | AAAAAAAA others(11): Show |
7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+19379_641+1938 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854557 | |||||
| chr8:96854557
|
A | AAAACAC | 8 | a0001c0001t0001g0056a0001c0002t0001g0072a0001c0002t0001g0093others(5): Show | 8 | HG01978.hp2 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+19379_641+1938 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854557 | |||||
| chr8:96854557
|
A | AAACAC | 20 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0117others(17): Show | 20 | HG01255.hp1 HG01884.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.641+19379_641+1938 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854557 | |||||
| chr8:96854557
|
A | AACAC | 12 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(9): Show | 12 | HG00099.hp1 HG00733.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+19378_641+1937 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96854557 | |||||
| chr8:96854557
|
A | C | 6 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.641+19377A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854557 | ||||||
| chr8:96854604
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.641+19424A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854604 | ||||||
| chr8:96854854
|
G | A | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+19674G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854854 | ||||||
| chr8:96854877
|
G | A | 40 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(37): Show | 40 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.641+19697G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96854877 | ||||||
| chr8:96855416
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+20236G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855416 | ||||||
| chr8:96855481
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+20301A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855481 | ||||||
| chr8:96855789
|
A | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.641+20609A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855789 | ||||||
| chr8:96855790
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+20610G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855790 | ||||||
| chr8:96855847
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.641+20667G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855847 | ||||||
| chr8:96855862
|
T | C | 9 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(6): Show | 9 | HG00099.hp2 HG01255.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.641+20682T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855862 | ||||||
| chr8:96855968
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.641+20788C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96855968 | ||||||
| chr8:96856538
|
T | G | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+21358T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96856538 | ||||||
| chr8:96856658
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+21478T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96856658 | ||||||
| chr8:96856690
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641+21510C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96856690 | ||||||
| chr8:96856772
|
G | T | 2 | a0004c0006t0001g0074a0004c0006t0001g0075 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.641+21592G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96856772 | ||||||
| chr8:96856810
|
T | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.641+21630T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96856810 | ||||||
| chr8:96857293
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+22113C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96857293 | ||||||
| chr8:96857338
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.641+22158C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96857338 | ||||||
| chr8:96857668
|
C | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(58): Show | 61 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.642-22130C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96857668 | ||||||
| chr8:96857841
|
T | TA | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-21956dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96857841 | |||||
| chr8:96858054
|
G | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(47): Show | 50 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.642-21744G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96858054 | ||||||
| chr8:96858341
|
T | C | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-21457T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96858341 | ||||||
| chr8:96858375
|
C | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | NA18747.hp1 NA18962.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-21423C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96858375 | ||||||
| chr8:96858443
|
G | A | 37 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.642-21355G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96858443 | ||||||
| chr8:96858778
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642-21020T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96858778 | ||||||
| chr8:96859159
|
G | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.642-20639G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859159 | ||||||
| chr8:96859219
|
C | G | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.642-20579C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859219 | ||||||
| chr8:96859469
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-20329C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859469 | ||||||
| chr8:96859508
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.642-20290T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859508 | ||||||
| chr8:96859526
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642-20272C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859526 | ||||||
| chr8:96859529
|
G | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.642-20269G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859529 | ||||||
| chr8:96859561
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.642-20237C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859561 | ||||||
| chr8:96859664
|
C | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.642-20134C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859664 | ||||||
| chr8:96859776
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-20022T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96859776 | ||||||
| chr8:96860079
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-19719T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96860079 | ||||||
| chr8:96860107
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.642-19691C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96860107 | ||||||
| chr8:96860171
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642-19627G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96860171 | ||||||
| chr8:96860471
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.642-19327G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96860471 | ||||||
| chr8:96860814
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-18984C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96860814 | ||||||
| chr8:96860955
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.642-18843A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96860955 | ||||||
| chr8:96861018
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642-18780T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861018 | ||||||
| chr8:96861078
|
T | A | 16 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(13): Show | 16 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.642-18720T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861078 | ||||||
| chr8:96861108
|
C | A | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642-18690C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861108 | ||||||
| chr8:96861171
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-18627T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861171 | ||||||
| chr8:96861373
|
C | T | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.642-18425C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861373 | ||||||
| chr8:96861447
|
A | G | 42 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(39): Show | 42 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.642-18351A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861447 | ||||||
| chr8:96861507
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-18291G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861507 | ||||||
| chr8:96861576
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-18222C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861576 | ||||||
| chr8:96861698
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-18100G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96861698 | ||||||
| chr8:96862004
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.642-17794G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96862004 | ||||||
| chr8:96862284
|
T | TTG | 6 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0002g0012others(3): Show | 6 | HG02004.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-17478_642-1747 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96862284 | |||||
| chr8:96862284
|
T | TTGTG | 6 | a0001c0001t0001g0030a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.642-17480_642-1747 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96862284 | |||||
| chr8:96862284
|
T | TTGTGTG | 4 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(1): Show | 4 | HG02004.hp2 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-17482_642-1747 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96862284 | |||||
| chr8:96862284
|
T | TTGTGTGT others(3): Show |
2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642-17486_642-1747 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96862284 | |||||
| chr8:96862284
|
TTG | T | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(55): Show | 58 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.642-17478_642-1747 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96862284 | |||||
| chr8:96862540
|
T | C | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.642-17258T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96862540 | ||||||
| chr8:96862953
|
A | G | 1 | a0001c0002t0002g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.642-16845A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96862953 | ||||||
| chr8:96863087
|
C | G | 62 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 62 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.642-16711C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863087 | ||||||
| chr8:96863417
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.642-16381G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863417 | ||||||
| chr8:96863444
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-16354A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863444 | ||||||
| chr8:96863459
|
A | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.642-16339A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863459 | ||||||
| chr8:96863576
|
G | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.642-16222G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863576 | ||||||
| chr8:96863608
|
C | A | 6 | a0001c0002t0001g0025a0001c0002t0001g0055a0001c0002t0001g0059others(3): Show | 6 | HG01261.hp1 HG01975.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-16190C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863608 | ||||||
| chr8:96863743
|
G | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.642-16055G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863743 | ||||||
| chr8:96863794
|
C | T | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.642-16004C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863794 | ||||||
| chr8:96863805
|
T | C | 2 | a0005c0013t0001g0043a0009c0012t0001g0090 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.642-15993T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863805 | ||||||
| chr8:96863973
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-15825G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96863973 | ||||||
| chr8:96864169
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642-15629T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864169 | ||||||
| chr8:96864183
|
A | G | 5 | a0001c0001t0001g0028a0001c0002t0001g0092a0001c0002t0001g0093others(2): Show | 5 | HG02004.hp2 HG02630.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-15615A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864183 | ||||||
| chr8:96864255
|
A | T | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-15543A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864255 | ||||||
| chr8:96864336
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.642-15462C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864336 | ||||||
| chr8:96864617
|
C | CTTGT | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.642-15181_642-1518 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864617 | ||||||
| chr8:96864735
|
A | G | 5 | a0001c0001t0001g0028a0001c0002t0001g0092a0001c0002t0001g0093others(2): Show | 5 | HG02004.hp2 HG02630.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-15063A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864735 | ||||||
| chr8:96864756
|
T | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.642-15042T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864756 | ||||||
| chr8:96864757
|
G | A | 60 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(57): Show | 60 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.642-15041G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864757 | ||||||
| chr8:96864913
|
A | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-14885A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96864913 | ||||||
| chr8:96865061
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.642-14737T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96865061 | ||||||
| chr8:96865091
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-14707A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96865091 | ||||||
| chr8:96865094
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-14704A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96865094 | ||||||
| chr8:96865178
|
C | G | 61 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(58): Show | 61 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.642-14620C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96865178 | ||||||
| chr8:96865668
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-14130C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96865668 | ||||||
| chr8:96865989
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-13809A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96865989 | ||||||
| chr8:96866277
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-13521G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96866277 | ||||||
| chr8:96866501
|
C | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(97): Show | 100 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(97): Show |
intron_variant | MODIFIER | c.642-13297C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96866501 | ||||||
| chr8:96866752
|
T | C | 2 | a0001c0002t0001g0081a0001c0002t0002g0082 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.642-13046T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96866752 | ||||||
| chr8:96866776
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.642-13022A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96866776 | ||||||
| chr8:96866912
|
C | G | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.642-12886C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96866912 | ||||||
| chr8:96867144
|
A | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(94): Show |
intron_variant | MODIFIER | c.642-12654A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96867144 | ||||||
| chr8:96867537
|
A | G | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.642-12261A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96867537 | ||||||
| chr8:96867586
|
A | G | 6 | a0001c0001t0001g0028a0001c0002t0001g0088a0001c0002t0001g0091others(3): Show | 6 | HG02647.hp1 HG02895.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-12212A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96867586 | ||||||
| chr8:96867601
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-12197C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96867601 | ||||||
| chr8:96867912
|
C | G | 37 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.642-11886C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96867912 | ||||||
| chr8:96867920
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-11878A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96867920 | ||||||
| chr8:96868138
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-11660C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96868138 | ||||||
| chr8:96868581
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642-11217A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96868581 | ||||||
| chr8:96868627
|
A | T | 6 | a0001c0001t0001g0028a0001c0002t0001g0088a0001c0002t0001g0091others(3): Show | 6 | HG02647.hp1 HG02895.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-11171A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96868627 | ||||||
| chr8:96869247
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.642-10551C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96869247 | ||||||
| chr8:96869315
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-10483T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96869315 | ||||||
| chr8:96869564
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.642-10234C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96869564 | ||||||
| chr8:96869847
|
T | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-9951T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96869847 | ||||||
| chr8:96869870
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.642-9928A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96869870 | ||||||
| chr8:96870046
|
T | G | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.642-9752T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870046 | ||||||
| chr8:96870096
|
G | A | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-9702G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870096 | ||||||
| chr8:96870166
|
AT | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(47): Show | 50 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.642-9625delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96870166 | |||||
| chr8:96870311
|
G | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642-9487G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870311 | ||||||
| chr8:96870381
|
G | A | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-9417G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870381 | ||||||
| chr8:96870413
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-9385A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870413 | ||||||
| chr8:96870618
|
T | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-9180T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870618 | ||||||
| chr8:96870628
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-9170A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870628 | ||||||
| chr8:96870706
|
C | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.642-9092C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870706 | ||||||
| chr8:96870862
|
G | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(3): Show | 6 | HG01081.hp1 NA18747.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.642-8936G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96870862 | ||||||
| chr8:96871088
|
AG | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-8709delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96871088 | ||||||
| chr8:96871105
|
G | T | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(42): Show | 45 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.642-8693G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96871105 | ||||||
| chr8:96871166
|
C | T | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.642-8632C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96871166 | ||||||
| chr8:96871531
|
G | GT | 13 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0070others(10): Show | 13 | HG01516.hp1 HG01517.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.642-8242dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96871531 | |||||
| chr8:96871531
|
GT | G | 11 | a0001c0001t0001g0063a0001c0001t0002g0099a0001c0002t0001g0084others(8): Show | 11 | HG00733.hp1 HG01943.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.642-8242delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96871531 | |||||
| chr8:96871531
|
GTT | G | 33 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(30): Show | 33 | HG00099.hp1 HG01255.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.642-8243_642-8242d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96871531 | |||||
| chr8:96871531
|
GTTT | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(13): Show | 16 | HG00733.hp2 HG01975.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.642-8244_642-8242d others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96871531 | |||||
| chr8:96871722
|
G | T | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-8076G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96871722 | ||||||
| chr8:96871846
|
G | C | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(60): Show | 63 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.642-7952G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96871846 | ||||||
| chr8:96872065
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-7733T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96872065 | ||||||
| chr8:96872244
|
A | T | 2 | a0005c0013t0001g0043a0009c0012t0001g0090 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.642-7554A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96872244 | ||||||
| chr8:96872472
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.642-7326T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96872472 | ||||||
| chr8:96872670
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.642-7128C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96872670 | ||||||
| chr8:96873041
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.642-6757C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96873041 | ||||||
| chr8:96873191
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-6607A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96873191 | ||||||
| chr8:96873317
|
C | CT | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-6471dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96873317 | |||||
| chr8:96873504
|
A | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-6294A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96873504 | ||||||
| chr8:96874600
|
C | CT | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-5192dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 96874600 | |||||
| chr8:96874958
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-4840A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96874958 | ||||||
| chr8:96875018
|
C | A | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.642-4780C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96875018 | ||||||
| chr8:96875092
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.642-4706C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96875092 | ||||||
| chr8:96875162
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.642-4636G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96875162 | ||||||
| chr8:96875437
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-4361T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96875437 | ||||||
| chr8:96875594
|
G | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.642-4204G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96875594 | ||||||
| chr8:96876149
|
A | G | 29 | a0001c0001t0001g0017a0001c0002t0001g0002a0001c0002t0001g0003others(26): Show | 29 | HG01081.hp2 HG01261.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.642-3649A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96876149 | ||||||
| chr8:96876422
|
A | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.642-3376A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96876422 | ||||||
| chr8:96876429
|
T | A | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.642-3369T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96876429 | ||||||
| chr8:96876431
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-3367T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96876431 | ||||||
| chr8:96877010
|
A | C | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642-2788A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877010 | ||||||
| chr8:96877260
|
C | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-2538C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877260 | ||||||
| chr8:96877557
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-2241T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877557 | ||||||
| chr8:96877576
|
C | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-2222C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877576 | ||||||
| chr8:96877576
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-2222C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877576 | ||||||
| chr8:96877578
|
A | G | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-2220A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877578 | ||||||
| chr8:96877620
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.642-2178A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877620 | ||||||
| chr8:96877623
|
T | G | 4 | a0001c0002t0001g0088a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG02895.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-2175T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877623 | ||||||
| chr8:96877634
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-2164A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877634 | ||||||
| chr8:96877745
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642-2053G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877745 | ||||||
| chr8:96877925
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.642-1873C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877925 | ||||||
| chr8:96877986
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-1812G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96877986 | ||||||
| chr8:96878031
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-1767C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878031 | ||||||
| chr8:96878033
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.642-1765G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878033 | ||||||
| chr8:96878132
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642-1666A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878132 | ||||||
| chr8:96878219
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-1579G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878219 | ||||||
| chr8:96878333
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-1465C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878333 | ||||||
| chr8:96878390
|
T | A | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.642-1408T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878390 | ||||||
| chr8:96878429
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.642-1369T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878429 | ||||||
| chr8:96878702
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-1096G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878702 | ||||||
| chr8:96878761
|
G | A | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.642-1037G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878761 | ||||||
| chr8:96878879
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642-919C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878879 | ||||||
| chr8:96878910
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642-888T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878910 | ||||||
| chr8:96878915
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-883C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96878915 | ||||||
| chr8:96879003
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.642-795T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96879003 | ||||||
| chr8:96879239
|
A | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-559A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96879239 | ||||||
| chr8:96879294
|
G | C | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.642-504G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96879294 | ||||||
| chr8:96879460
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0002g0067 | 3 | HG01255.hp1 HG01516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.642-338G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 3/7 | chr8 | 96879460 | ||||||
| chr8:96880022
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+17G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880022 | ||||||
| chr8:96880120
|
G | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(60): Show | 63 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.849+115G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880120 | ||||||
| chr8:96880486
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+481A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880486 | ||||||
| chr8:96880516
|
G | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+511G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880516 | ||||||
| chr8:96880518
|
CAT | C | 5 | a0001c0001t0001g0057a0001c0001t0001g0109a0001c0002t0001g0073others(2): Show | 5 | HG00099.hp1 HG02886.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+571_849+572del others(2): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATAT | C | 8 | a0001c0001t0001g0080a0001c0001t0002g0067a0001c0001t0002g0100others(5): Show | 8 | HG01255.hp1 HG01884.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+569_849+572del others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATAT | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0056others(3): Show | 6 | HG01978.hp2 HG02273.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+567_849+572del others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(1): Show |
C | 2 | a0001c0001t0001g0063a0001c0001t0001g0117 | 2 | HG00733.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.849+565_849+572del others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0009a0001c0002t0002g0039 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.849+561_849+572del others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(7): Show |
C | 11 | a0001c0001t0001g0010a0001c0001t0002g0021a0001c0002t0001g0018others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.849+559_849+572del others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.849+557_849+572del others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(11): Show |
C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.849+555_849+572del others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(13): Show |
C | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.849+553_849+572del others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(15): Show |
C | 5 | a0001c0001t0001g0064a0001c0002t0001g0006a0001c0002t0001g0122others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+551_849+572del others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(17): Show |
C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.849+549_849+572del others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(19): Show |
C | 7 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG01255.hp2 HG01261.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.849+547_849+572del others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(21): Show |
C | 27 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(24): Show | 27 | HG00099.hp2 HG01081.hp1 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.849+545_849+572del others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(23): Show |
C | 3 | a0001c0001t0001g0110a0001c0001t0002g0044a0001c0002t0001g0069 | 3 | HG01081.hp2 HG02615.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.849+543_849+572del others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(25): Show |
C | 28 | a0001c0001t0001g0017a0001c0002t0001g0002a0001c0002t0001g0003others(25): Show | 28 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.849+541_849+572del others(32): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(27): Show |
C | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.849+539_849+572del others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(31): Show |
C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.849+535_849+572del others(38): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(33): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+533_849+572del others(40): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880518
|
CATATATA others(37): Show |
C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+529_849+572del others(44): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880518 | |||||
| chr8:96880574
|
T | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 63 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.849+569T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880574 | ||||||
| chr8:96880576
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(15): Show | 18 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+571T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880576 | ||||||
| chr8:96880576
|
T | TATATAC | 2 | a0001c0001t0001g0108a0001c0001t0002g0099 | 2 | HG02040.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.849+572_849+573ins others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880576 | |||||
| chr8:96880576
|
T | TATATATA others(11): Show |
1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+572_849+573ins others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96880576 | |||||
| chr8:96880739
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+734A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880739 | ||||||
| chr8:96880965
|
T | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+960T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96880965 | ||||||
| chr8:96881200
|
G | A | 37 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(34): Show | 37 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.849+1195G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96881200 | ||||||
| chr8:96881270
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+1265G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96881270 | ||||||
| chr8:96881389
|
A | C | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.849+1384A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96881389 | ||||||
| chr8:96881825
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.849+1820G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96881825 | ||||||
| chr8:96882248
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.849+2243A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96882248 | ||||||
| chr8:96882374
|
C | G | 2 | a0005c0013t0001g0043a0009c0012t0001g0090 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.849+2369C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96882374 | ||||||
| chr8:96882504
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+2499G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96882504 | ||||||
| chr8:96882514
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+2509C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96882514 | ||||||
| chr8:96882723
|
G | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(60): Show | 63 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.849+2718G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96882723 | ||||||
| chr8:96883047
|
G | A | 3 | a0001c0001t0002g0021a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | HG02109.hp1 HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.849+3042G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883047 | ||||||
| chr8:96883088
|
A | T | 2 | a0005c0013t0001g0043a0009c0012t0001g0090 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.849+3083A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883088 | ||||||
| chr8:96883241
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.849+3236T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883241 | ||||||
| chr8:96883553
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+3548T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883553 | ||||||
| chr8:96883622
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+3617C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883622 | ||||||
| chr8:96883702
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+3697A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883702 | ||||||
| chr8:96883808
|
T | C | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849+3803T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883808 | ||||||
| chr8:96883939
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+3934G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96883939 | ||||||
| chr8:96884336
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+4331C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96884336 | ||||||
| chr8:96884342
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+4337G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96884342 | ||||||
| chr8:96884342
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+4337G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96884342 | ||||||
| chr8:96884844
|
A | C | 6 | a0001c0001t0001g0028a0001c0002t0001g0088a0001c0002t0001g0091others(3): Show | 6 | HG02647.hp1 HG02895.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+4839A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96884844 | ||||||
| chr8:96885403
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+5398C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96885403 | ||||||
| chr8:96885465
|
A | G | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849+5460A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96885465 | ||||||
| chr8:96885723
|
T | C | 2 | a0001c0001t0001g0028a0001c0002t0001g0088 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.849+5718T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96885723 | ||||||
| chr8:96885754
|
C | T | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+5749C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96885754 | ||||||
| chr8:96885980
|
GA | G | 66 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(63): Show | 66 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.849+5985delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96885980 | |||||
| chr8:96886096
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+6091A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886096 | ||||||
| chr8:96886177
|
T | G | 2 | a0001c0001t0001g0028a0001c0002t0001g0088 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.849+6172T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886177 | ||||||
| chr8:96886251
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.849+6246C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886251 | ||||||
| chr8:96886471
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+6466T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886471 | ||||||
| chr8:96886556
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+6551G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886556 | ||||||
| chr8:96886672
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+6667A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886672 | ||||||
| chr8:96886678
|
C | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+6673C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886678 | ||||||
| chr8:96886738
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+6733C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886738 | ||||||
| chr8:96886749
|
T | A | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+6744T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886749 | ||||||
| chr8:96886791
|
G | A | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849+6786G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886791 | ||||||
| chr8:96886955
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.849+6950A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886955 | ||||||
| chr8:96886958
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+6953C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886958 | ||||||
| chr8:96886958
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.849+6953C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886958 | ||||||
| chr8:96886976
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+6971T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96886976 | ||||||
| chr8:96887093
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.849+7088C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96887093 | ||||||
| chr8:96887397
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+7392C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96887397 | ||||||
| chr8:96887491
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+7486A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96887491 | ||||||
| chr8:96887593
|
ACT | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(60): Show | 63 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.849+7596_849+7597d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96887593 | |||||
| chr8:96887812
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+7807T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96887812 | ||||||
| chr8:96888089
|
G | A | 59 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(56): Show | 59 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.849+8084G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888089 | ||||||
| chr8:96888211
|
T | G | 1 | a0001c0002t0001g0121 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.849+8206T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888211 | ||||||
| chr8:96888214
|
G | A | 18 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0049others(15): Show | 18 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.849+8209G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888214 | ||||||
| chr8:96888639
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+8634G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888639 | ||||||
| chr8:96888885
|
C | T | 83 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(80): Show | 83 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.849+8880C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888885 | ||||||
| chr8:96888960
|
A | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+8955A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888960 | ||||||
| chr8:96888975
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+8970A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96888975 | ||||||
| chr8:96889191
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.849+9186G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96889191 | ||||||
| chr8:96889691
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+9686C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96889691 | ||||||
| chr8:96890100
|
A | G | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+10095A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890100 | ||||||
| chr8:96890115
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+10110C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890115 | ||||||
| chr8:96890197
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.849+10192C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890197 | ||||||
| chr8:96890201
|
A | G | 4 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+10196A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890201 | ||||||
| chr8:96890874
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.849+10869C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890874 | ||||||
| chr8:96890953
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.849+10948A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890953 | ||||||
| chr8:96890990
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+10985C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890990 | ||||||
| chr8:96890999
|
G | A | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.849+10994G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96890999 | ||||||
| chr8:96891006
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+11001C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891006 | ||||||
| chr8:96891197
|
T | C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.849+11192T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891197 | ||||||
| chr8:96891294
|
G | A | 2 | a0002c0003t0001g0008a0002c0003t0001g0015 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+11289G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891294 | ||||||
| chr8:96891378
|
G | A | 41 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(38): Show | 41 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.849+11373G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891378 | ||||||
| chr8:96891703
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+11698G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891703 | ||||||
| chr8:96891760
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+11755C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891760 | ||||||
| chr8:96891765
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.849+11760T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96891765 | ||||||
| chr8:96892040
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.849+12035G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96892040 | ||||||
| chr8:96892196
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(75): Show | 78 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.849+12191G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96892196 | ||||||
| chr8:96892209
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.849+12204A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96892209 | ||||||
| chr8:96892523
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+12518G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96892523 | ||||||
| chr8:96892691
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.849+12686C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96892691 | ||||||
| chr8:96892764
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+12759T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96892764 | ||||||
| chr8:96893218
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+13213G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96893218 | ||||||
| chr8:96893286
|
A | G | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.849+13281A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96893286 | ||||||
| chr8:96893294
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+13289C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96893294 | ||||||
| chr8:96893571
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+13566G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96893571 | ||||||
| chr8:96893870
|
A | T | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.849+13865A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96893870 | ||||||
| chr8:96894624
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+14619A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96894624 | ||||||
| chr8:96894701
|
A | T | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.849+14696A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96894701 | ||||||
| chr8:96895049
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.849+15044C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96895049 | ||||||
| chr8:96895388
|
G | A | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.849+15383G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96895388 | ||||||
| chr8:96895445
|
G | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+15440G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96895445 | ||||||
| chr8:96895650
|
A | G | 3 | a0001c0001t0001g0034a0001c0002t0001g0088a0001c0002t0001g0091 | 3 | HG01081.hp1 HG02895.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.849+15645A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96895650 | ||||||
| chr8:96895834
|
A | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+15829A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96895834 | ||||||
| chr8:96895864
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(10): Show | 13 | HG00733.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.849+15859G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96895864 | ||||||
| chr8:96896030
|
G | A | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+16025G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896030 | ||||||
| chr8:96896113
|
C | G | 3 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+16108C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896113 | ||||||
| chr8:96896122
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+16117C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896122 | ||||||
| chr8:96896173
|
T | C | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+16168T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896173 | ||||||
| chr8:96896290
|
G | A | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.849+16285G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896290 | ||||||
| chr8:96896346
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+16341C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896346 | ||||||
| chr8:96896408
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+16403C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896408 | ||||||
| chr8:96896527
|
A | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+16522A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896527 | ||||||
| chr8:96896599
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+16594A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896599 | ||||||
| chr8:96896695
|
G | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+16690G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896695 | ||||||
| chr8:96896717
|
T | C | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.849+16712T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896717 | ||||||
| chr8:96896810
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+16805T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896810 | ||||||
| chr8:96896913
|
T | A | 3 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+16908T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96896913 | ||||||
| chr8:96897227
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+17222A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897227 | ||||||
| chr8:96897234
|
A | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+17229A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897234 | ||||||
| chr8:96897239
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+17234T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897239 | ||||||
| chr8:96897421
|
G | A | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.849+17416G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897421 | ||||||
| chr8:96897480
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.849+17475T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897480 | ||||||
| chr8:96897716
|
C | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+17711C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897716 | ||||||
| chr8:96897739
|
T | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+17734T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897739 | ||||||
| chr8:96897814
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.849+17809T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897814 | ||||||
| chr8:96897816
|
G | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+17811G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897816 | ||||||
| chr8:96897830
|
G | A | 2 | a0001c0002t0001g0055a0001c0002t0001g0059 | 2 | HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.849+17825G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897830 | ||||||
| chr8:96897859
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+17854C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96897859 | ||||||
| chr8:96898051
|
CGTT | C | 61 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(58): Show | 61 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.849+18050_849+1805 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96898051 | |||||
| chr8:96898354
|
C | T | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.849+18349C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96898354 | ||||||
| chr8:96898467
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+18462G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96898467 | ||||||
| chr8:96898542
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.849+18537G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96898542 | ||||||
| chr8:96898776
|
T | TA | 63 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 63 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.849+18788dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96898776 | |||||
| chr8:96898776
|
T | TAA | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+18787_849+1878 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96898776 | |||||
| chr8:96898776
|
TA | T | 27 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(24): Show | 27 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.849+18788delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96898776 | |||||
| chr8:96898776
|
TAA | T | 12 | a0001c0001t0002g0021a0001c0002t0001g0073a0001c0002t0001g0088others(9): Show | 12 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+18787_849+1878 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96898776 | |||||
| chr8:96898777
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+18772A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96898777 | ||||||
| chr8:96898838
|
G | GT | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(9): Show | 12 | HG00733.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+18834dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96898838 | |||||
| chr8:96898842
|
C | T | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.849+18837C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96898842 | ||||||
| chr8:96898859
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.849+18854A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96898859 | ||||||
| chr8:96899392
|
G | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+19387G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96899392 | ||||||
| chr8:96899511
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+19506C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96899511 | ||||||
| chr8:96899516
|
C | T | 3 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+19511C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96899516 | ||||||
| chr8:96899579
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+19574C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96899579 | ||||||
| chr8:96899585
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+19580G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96899585 | ||||||
| chr8:96899587
|
G | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+19582G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96899587 | ||||||
| chr8:96899743
|
C | CACTAGGG others(55): Show |
1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.849+19739_849+1980 others(66): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96899743 | |||||
| chr8:96900030
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+20025C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96900030 | ||||||
| chr8:96900226
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.849+20221C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96900226 | ||||||
| chr8:96900424
|
A | G | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.849+20419A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96900424 | ||||||
| chr8:96900579
|
T | G | 1 | a0001c0002t0001g0058 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.849+20574T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96900579 | ||||||
| chr8:96900634
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+20629G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96900634 | ||||||
| chr8:96900658
|
T | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+20653T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96900658 | ||||||
| chr8:96901069
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+21064C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96901069 | ||||||
| chr8:96901290
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+21285C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96901290 | ||||||
| chr8:96901733
|
T | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(22): Show | 25 | HG00733.hp2 HG02004.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.849+21728T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96901733 | ||||||
| chr8:96901978
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+21973G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96901978 | ||||||
| chr8:96902002
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.849+21997A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902002 | ||||||
| chr8:96902091
|
A | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(9): Show | 12 | HG00733.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+22086A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902091 | ||||||
| chr8:96902253
|
G | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+22248G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902253 | ||||||
| chr8:96902422
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849+22417T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902422 | ||||||
| chr8:96902452
|
A | C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+22447A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902452 | ||||||
| chr8:96902546
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.849+22541G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902546 | ||||||
| chr8:96902573
|
C | G | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+22568C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902573 | ||||||
| chr8:96902595
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+22590G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902595 | ||||||
| chr8:96902665
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+22660G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902665 | ||||||
| chr8:96902743
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.849+22738C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902743 | ||||||
| chr8:96902770
|
G | A | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849+22765G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902770 | ||||||
| chr8:96902803
|
A | C | 8 | a0001c0002t0001g0025a0001c0002t0001g0055a0001c0002t0001g0059others(5): Show | 8 | HG01261.hp1 HG01943.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+22798A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902803 | ||||||
| chr8:96902905
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.849+22900G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96902905 | ||||||
| chr8:96903080
|
G | C | 1 | a0001c0002t0001g0058 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.849+23075G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96903080 | ||||||
| chr8:96903433
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+23428A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96903433 | ||||||
| chr8:96903695
|
C | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077 | 3 | NA18945.hp2 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.849+23690C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96903695 | ||||||
| chr8:96903707
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+23702A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96903707 | ||||||
| chr8:96904027
|
A | C | 61 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(58): Show | 61 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.849+24022A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96904027 | ||||||
| chr8:96904098
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.849+24093A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96904098 | ||||||
| chr8:96904160
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.849+24155T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96904160 | ||||||
| chr8:96904228
|
CCT | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(97): Show | 100 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(97): Show |
intron_variant | MODIFIER | c.849+24227_849+2422 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96904228 | |||||
| chr8:96904267
|
A | C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.849+24262A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96904267 | ||||||
| chr8:96904536
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+24531G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96904536 | ||||||
| chr8:96905385
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.849+25380A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96905385 | ||||||
| chr8:96905760
|
CA | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0110others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+25778delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96905760 | |||||
| chr8:96906071
|
GC | G | 22 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0002t0001g0002others(19): Show | 22 | HG01081.hp2 HG01255.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.849+26070delC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96906071 | |||||
| chr8:96906081
|
A | G | 2 | a0001c0002t0001g0055a0001c0002t0001g0059 | 2 | HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.849+26076A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906081 | ||||||
| chr8:96906276
|
G | T | 38 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0046others(35): Show | 38 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.849+26271G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906276 | ||||||
| chr8:96906327
|
T | C | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.849+26322T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906327 | ||||||
| chr8:96906469
|
A | C | 3 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+26464A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906469 | ||||||
| chr8:96906642
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.849+26637A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906642 | ||||||
| chr8:96906776
|
C | T | 1 | a0002c0003t0001g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.849+26771C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906776 | ||||||
| chr8:96906913
|
T | C | 3 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+26908T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96906913 | ||||||
| chr8:96907052
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+27047A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907052 | ||||||
| chr8:96907285
|
G | A | 22 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0002t0001g0002others(19): Show | 22 | HG01081.hp2 HG01255.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.849+27280G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907285 | ||||||
| chr8:96907391
|
C | G | 3 | a0001c0001t0001g0028a0005c0013t0001g0043a0009c0012t0001g0090 | 3 | HG02965.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.849+27386C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907391 | ||||||
| chr8:96907518
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.849+27513C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907518 | ||||||
| chr8:96907702
|
C | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.849+27697C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907702 | ||||||
| chr8:96907875
|
A | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+27870A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907875 | ||||||
| chr8:96907929
|
A | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(40): Show | 43 | HG00733.hp2 HG01081.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+27924A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96907929 | ||||||
| chr8:96908107
|
C | CGT | 32 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0042others(29): Show | 32 | HG00733.hp1 HG00733.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.849+28137_849+2813 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
C | CGTGT | 4 | a0001c0001t0001g0041a0002c0003t0001g0052a0002c0003t0001g0053others(1): Show | 4 | HG00099.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+28135_849+2813 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
C | CGTGTGT | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0005c0013t0001g0043others(1): Show | 4 | HG01943.hp1 HG02273.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+28133_849+2813 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
CGT | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(3): Show | 6 | HG02055.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+28137_849+2813 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
CGTGT | C | 21 | a0001c0001t0001g0104a0001c0001t0002g0020a0001c0002t0001g0002others(18): Show | 21 | HG01081.hp2 HG01255.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.849+28135_849+2813 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
CGTGTGT | C | 45 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(42): Show | 45 | HG01081.hp1 HG01261.hp1 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+28133_849+2813 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
CGTGTGTG others(1): Show |
C | 5 | a0001c0001t0001g0026a0001c0002t0001g0123a0001c0007t0001g0038others(2): Show | 5 | HG00099.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+28131_849+2813 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.849+28129_849+2813 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908107
|
CGTGTGTG others(5): Show |
C | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004others(1): Show | 4 | HG02004.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+28127_849+2813 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908107 | |||||
| chr8:96908703
|
G | A | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+28698G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96908703 | ||||||
| chr8:96908747
|
G | GCACA | 5 | a0001c0001t0001g0028a0001c0002t0002g0039a0002c0003t0001g0054others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+28770_849+2877 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCACACA | 65 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.849+28768_849+2877 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCACACAC others(1): Show |
15 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00733.hp2 HG01261.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.849+28766_849+2877 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCACACAC others(3): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(5): Show | 8 | HG00733.hp1 HG02647.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+28764_849+2877 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCACACAC others(5): Show |
2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.849+28762_849+2877 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCGCA | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.849+28743_849+2874 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCGCACAC others(1): Show |
17 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0002t0001g0049others(14): Show | 17 | HG01081.hp2 HG01255.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.849+28743_849+2874 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCGCGCGC others(9): Show |
2 | a0001c0002t0001g0005a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.849+28743_849+2874 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908747
|
G | GCGCGCGC others(13): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0122 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.849+28743_849+2874 others(24): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908747 | |||||
| chr8:96908749
|
A | G | 2 | a0001c0002t0001g0084a0001c0002t0001g0101 | 2 | HG02970.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.849+28744A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96908749 | ||||||
| chr8:96908777
|
A | ACACACAC others(3): Show |
1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+28773_849+2877 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96908777 | |||||
| chr8:96908777
|
A | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0002t0001g0002others(17): Show | 20 | HG01081.hp2 HG01255.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.849+28772A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96908777 | ||||||
| chr8:96908898
|
C | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.849+28893C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96908898 | ||||||
| chr8:96909011
|
T | A | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.849+29006T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909011 | ||||||
| chr8:96909353
|
T | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(16): Show | 19 | HG00733.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.849+29348T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909353 | ||||||
| chr8:96909621
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.849+29616G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909621 | ||||||
| chr8:96909624
|
A | G | 1 | a0001c0002t0002g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.849+29619A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909624 | ||||||
| chr8:96909784
|
C | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp2 HG00733.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.849+29779C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909784 | ||||||
| chr8:96909823
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0063others(1): Show | 4 | HG00733.hp1 HG01255.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+29818G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909823 | ||||||
| chr8:96909917
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0122others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+29912C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96909917 | ||||||
| chr8:96910154
|
G | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(41): Show | 44 | HG00099.hp2 HG01081.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.849+30149G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96910154 | ||||||
| chr8:96910520
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849+30515T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96910520 | ||||||
| chr8:96910524
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.849+30519A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96910524 | ||||||
| chr8:96910554
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.849+30549G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96910554 | ||||||
| chr8:96910665
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+30660T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96910665 | ||||||
| chr8:96910949
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+30944T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96910949 | ||||||
| chr8:96911121
|
A | G | 3 | a0001c0002t0001g0091a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+31116A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96911121 | ||||||
| chr8:96911203
|
T | TACAAA | 8 | a0001c0002t0001g0025a0001c0002t0001g0055a0001c0002t0001g0059others(5): Show | 8 | HG01261.hp1 HG01943.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+31212_849+3121 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96911203 | |||||
| chr8:96911572
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+31567T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96911572 | ||||||
| chr8:96911960
|
G | A | 3 | a0001c0001t0002g0044a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | HG02615.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+31955G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96911960 | ||||||
| chr8:96911963
|
A | G | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.849+31958A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96911963 | ||||||
| chr8:96912396
|
A | G | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.849+32391A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96912396 | ||||||
| chr8:96912438
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.849+32433T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96912438 | ||||||
| chr8:96912568
|
G | A | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+32563G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96912568 | ||||||
| chr8:96912711
|
C | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+32706C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96912711 | ||||||
| chr8:96912908
|
C | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0056others(10): Show | 13 | HG00733.hp1 HG01516.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.849+32903C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96912908 | ||||||
| chr8:96912978
|
G | A | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+32973G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96912978 | ||||||
| chr8:96913426
|
A | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103 | 3 | HG01975.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.849+33421A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96913426 | ||||||
| chr8:96913637
|
G | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+33632G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96913637 | ||||||
| chr8:96914036
|
CAA | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004 | 3 | HG02257.hp2 HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.849+34034_849+3403 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96914036 | |||||
| chr8:96914124
|
T | C | 7 | a0001c0001t0002g0021a0001c0002t0001g0092a0001c0002t0001g0093others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+34119T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96914124 | ||||||
| chr8:96914169
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.849+34164G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96914169 | ||||||
| chr8:96914184
|
T | G | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+34179T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96914184 | ||||||
| chr8:96914568
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+34563A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96914568 | ||||||
| chr8:96914615
|
G | T | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+34610G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96914615 | ||||||
| chr8:96914688
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+34683G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96914688 | ||||||
| chr8:96915015
|
A | T | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.849+35010A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96915015 | ||||||
| chr8:96915242
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.849+35237G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96915242 | ||||||
| chr8:96915685
|
T | G | 11 | a0001c0001t0001g0027a0001c0002t0001g0025a0001c0002t0001g0055others(8): Show | 11 | HG00099.hp1 HG01261.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.849+35680T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96915685 | ||||||
| chr8:96916209
|
G | T | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.849+36204G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96916209 | ||||||
| chr8:96916478
|
A | C | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+36473A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96916478 | ||||||
| chr8:96916695
|
G | A | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+36690G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96916695 | ||||||
| chr8:96917105
|
T | G | 39 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0033others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.849+37100T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96917105 | ||||||
| chr8:96917383
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+37378C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96917383 | ||||||
| chr8:96917665
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.849+37660A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96917665 | ||||||
| chr8:96918162
|
G | C | 41 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(38): Show | 41 | HG00099.hp2 HG00733.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.849+38157G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918162 | ||||||
| chr8:96918210
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.849+38205T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918210 | ||||||
| chr8:96918311
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+38306T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918311 | ||||||
| chr8:96918523
|
T | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004 | 3 | HG02257.hp2 HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.849+38518T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918523 | ||||||
| chr8:96918594
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.849+38589C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918594 | ||||||
| chr8:96918699
|
C | G | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.849+38694C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918699 | ||||||
| chr8:96918911
|
C | T | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+38906C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96918911 | ||||||
| chr8:96919129
|
C | CT | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+39133dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96919129 | |||||
| chr8:96919210
|
C | T | 3 | a0001c0001t0002g0044a0001c0002t0001g0040a0002c0003t0001g0087 | 3 | HG01261.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.849+39205C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919210 | ||||||
| chr8:96919267
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+39262A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919267 | ||||||
| chr8:96919293
|
G | A | 37 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0033others(34): Show | 37 | HG00099.hp2 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.849+39288G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919293 | ||||||
| chr8:96919338
|
C | T | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+39333C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919338 | ||||||
| chr8:96919743
|
T | C | 37 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0033others(34): Show | 37 | HG00099.hp2 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.849+39738T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919743 | ||||||
| chr8:96919751
|
A | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+39746A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919751 | ||||||
| chr8:96919816
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.849+39811T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919816 | ||||||
| chr8:96919816
|
T | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(90): Show | 93 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.849+39811T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96919816 | ||||||
| chr8:96920093
|
G | A | 71 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0028others(68): Show | 71 | HG00099.hp2 HG00733.hp1 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.849+40088G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920093 | ||||||
| chr8:96920143
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.849+40138C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920143 | ||||||
| chr8:96920159
|
G | C | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.849+40154G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920159 | ||||||
| chr8:96920206
|
G | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+40201G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920206 | ||||||
| chr8:96920372
|
T | A | 7 | a0001c0001t0002g0021a0001c0002t0001g0092a0001c0002t0001g0093others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+40367T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920372 | ||||||
| chr8:96920381
|
G | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+40376G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920381 | ||||||
| chr8:96920478
|
G | C | 37 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0033others(34): Show | 37 | HG00099.hp2 HG00733.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.849+40473G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920478 | ||||||
| chr8:96920612
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.849+40607C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920612 | ||||||
| chr8:96920803
|
T | G | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0004 | 3 | HG02257.hp2 HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.849+40798T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920803 | ||||||
| chr8:96920905
|
G | C | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.849+40900G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920905 | ||||||
| chr8:96920937
|
C | T | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.849+40932C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96920937 | ||||||
| chr8:96921701
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.849+41696T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96921701 | ||||||
| chr8:96922071
|
T | TTTTTAAA others(6): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0008t0001g0116 | 3 | HG02647.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.849+42077_849+4208 others(17): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96922071 | |||||
| chr8:96922282
|
C | T | 38 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(35): Show | 38 | HG00099.hp2 HG00733.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.849+42277C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96922282 | ||||||
| chr8:96922929
|
TAGTC | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(41): Show | 44 | HG00733.hp2 HG01081.hp2 HG01516.hp1 others(41): Show |
intron_variant | MODIFIER | c.849+42929_849+4293 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96922929 | |||||
| chr8:96923060
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-42875A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96923060 | ||||||
| chr8:96923497
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.850-42438C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96923497 | ||||||
| chr8:96923666
|
C | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-42269C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96923666 | ||||||
| chr8:96923695
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.850-42240T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96923695 | ||||||
| chr8:96924526
|
A | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-41409A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96924526 | ||||||
| chr8:96924905
|
A | G | 2 | a0001c0002t0001g0079a0001c0002t0001g0124 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.850-41030A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96924905 | ||||||
| chr8:96924936
|
G | A | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.850-40999G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96924936 | ||||||
| chr8:96925011
|
T | C | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-40924T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96925011 | ||||||
| chr8:96925386
|
C | CT | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-40534dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96925386 | |||||
| chr8:96925629
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.850-40306C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96925629 | ||||||
| chr8:96925694
|
C | CT | 30 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-40227dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96925694 | |||||
| chr8:96926061
|
T | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-39874T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926061 | ||||||
| chr8:96926110
|
C | T | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-39825C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926110 | ||||||
| chr8:96926485
|
A | T | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.850-39450A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926485 | ||||||
| chr8:96926540
|
T | TTCTTCCT others(17): Show |
1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850-39377_850-3935 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926540 | |||||
| chr8:96926570
|
C | CTCTTCT | 2 | a0001c0002t0001g0081a0001c0002t0002g0082 | 2 | HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.850-39360_850-3935 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
C | CTCTTCTT others(5): Show |
3 | a0001c0001t0002g0044a0001c0002t0001g0040a0001c0002t0001g0123 | 3 | HG01261.hp2 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.850-39360_850-3935 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
C | CTCTTCTT others(8): Show |
3 | a0001c0002t0001g0005a0001c0002t0001g0084a0002c0003t0001g0087 | 3 | HG02280.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-39360_850-3935 others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
C | CTCTTCTT others(11): Show |
1 | a0002c0003t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.850-39360_850-3935 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
C | CTCTTCTT others(14): Show |
1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.850-39360_850-3935 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
C | CTCTTCTT others(29): Show |
1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.850-39360_850-3935 others(40): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
C | CTCTTCTT others(38): Show |
1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.850-39360_850-3935 others(49): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926570
|
CTCTTCCT others(2): Show |
C | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103 | 3 | HG01975.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.850-39359_850-3935 others(13): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926570 | |||||
| chr8:96926576
|
C | CTCT | 4 | a0001c0001t0001g0056a0001c0002t0001g0025a0001c0002t0001g0072others(1): Show | 4 | HG01261.hp1 HG01978.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-39313_850-3931 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(20): Show |
2 | a0001c0002t0001g0098a0004c0006t0001g0075 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(31): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(17): Show |
1 | a0001c0002t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-39354_850-3935 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(23): Show |
2 | a0001c0002t0001g0049a0001c0002t0001g0101 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(38): Show |
2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(49): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(11): Show |
1 | a0001c0002t0001g0121 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850-39354_850-3935 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(14): Show |
1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.850-39354_850-3935 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(17): Show |
3 | a0001c0002t0001g0058a0001c0002t0001g0065a0006c0010t0001g0045 | 3 | HG02004.hp2 NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(20): Show |
3 | a0001c0002t0001g0066a0001c0002t0001g0086a0001c0002t0001g0095 | 3 | NA18945.hp1 NA18990.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(31): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(23): Show |
2 | a0001c0002t0001g0097a0001c0002t0001g0106 | 2 | NA18979.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(26): Show |
1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.850-39354_850-3935 others(37): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(29): Show |
1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-39354_850-3935 others(40): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(5): Show |
3 | a0001c0001t0002g0021a0001c0002t0001g0069a0001c0002t0002g0004 | 3 | HG01081.hp2 HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(8): Show |
1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850-39354_850-3935 others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(11): Show |
4 | a0001c0001t0001g0023a0001c0002t0001g0088a0001c0002t0003g0001others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-39354_850-3935 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(14): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0002t0001g0096others(1): Show | 4 | HG00733.hp2 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-39354_850-3935 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(17): Show |
1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.850-39354_850-3935 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCCT others(23): Show |
3 | a0001c0001t0001g0034a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG01081.hp1 HG02004.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.850-39354_850-3935 others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCT | 2 | a0001c0001t0001g0047a0001c0001t0001g0112 | 2 | HG01943.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.850-39316_850-3931 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(2): Show |
6 | a0001c0001t0001g0078a0001c0002t0001g0055a0001c0002t0001g0059others(3): Show | 6 | HG01975.hp1 HG01978.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-39319_850-3931 others(13): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(5): Show |
9 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0061others(6): Show | 9 | HG01981.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-39322_850-3931 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(8): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0046others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-39325_850-3931 others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(11): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0002g0029others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-39328_850-3931 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(14): Show |
2 | a0001c0001t0001g0027a0001c0002t0001g0079 | 2 | HG01517.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.850-39331_850-3931 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(17): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0105a0001c0001t0002g0022others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-39334_850-3931 others(28): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(20): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0024a0005c0013t0001g0043 | 3 | HG02630.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.850-39337_850-3931 others(31): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(23): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0124others(1): Show | 4 | HG03195.hp1 HG04184.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-39340_850-3931 others(34): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(29): Show |
2 | a0001c0001t0002g0013a0001c0001t0004g0083 | 2 | HG03453.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.850-39346_850-3931 others(40): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | CTCTTCTT others(35): Show |
1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.850-39352_850-3931 others(46): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926576
|
C | T | 14 | a0001c0001t0001g0110a0001c0001t0002g0044a0001c0002t0001g0005others(11): Show | 14 | HG01261.hp2 HG01943.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.850-39359C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926576 | ||||||
| chr8:96926576
|
CTCT | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0001t0001g0102others(3): Show | 6 | HG00733.hp1 HG01255.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-39313_850-3931 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926576 | |||||
| chr8:96926582
|
T | C | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.850-39353T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926582 | ||||||
| chr8:96926588
|
T | C | 1 | a0001c0002t0001g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850-39347T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926588 | ||||||
| chr8:96926624
|
T | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.850-39311T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926624 | ||||||
| chr8:96926624
|
T | TTCTTCTT others(14): Show |
1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.850-39311_850-3931 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926624 | ||||||
| chr8:96926625
|
C | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(41): Show | 44 | HG00733.hp2 HG01081.hp2 HG01516.hp1 others(41): Show |
intron_variant | MODIFIER | c.850-39310C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926625 | ||||||
| chr8:96926628
|
C | T | 7 | a0001c0001t0002g0021a0001c0002t0001g0092a0001c0002t0001g0093others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-39307C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926628 | ||||||
| chr8:96926634
|
C | T | 7 | a0001c0001t0002g0021a0001c0002t0001g0092a0001c0002t0001g0093others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-39301C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926634 | ||||||
| chr8:96926643
|
T | TCTTCTTC others(5): Show |
1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-39287_850-3928 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96926643 | |||||
| chr8:96926745
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-39190G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96926745 | ||||||
| chr8:96927117
|
A | T | 32 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(29): Show | 32 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.850-38818A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96927117 | ||||||
| chr8:96927216
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.850-38719A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96927216 | ||||||
| chr8:96927326
|
C | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-38609C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96927326 | ||||||
| chr8:96927470
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-38465A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96927470 | ||||||
| chr8:96927532
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-38403G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96927532 | ||||||
| chr8:96927701
|
A | G | 5 | a0001c0002t0001g0084a0001c0002t0001g0091a0001c0004t0001g0107others(2): Show | 5 | HG02965.hp2 HG02970.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-38234A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96927701 | ||||||
| chr8:96928011
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.850-37924G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928011 | ||||||
| chr8:96928150
|
T | A | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.850-37785T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928150 | ||||||
| chr8:96928327
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-37608A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928327 | ||||||
| chr8:96928361
|
A | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-37574A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928361 | ||||||
| chr8:96928434
|
C | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-37501C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928434 | ||||||
| chr8:96928493
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.850-37442G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928493 | ||||||
| chr8:96928796
|
C | T | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.850-37139C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928796 | ||||||
| chr8:96928997
|
A | G | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-36938A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96928997 | ||||||
| chr8:96929019
|
A | T | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-36916A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929019 | ||||||
| chr8:96929098
|
C | T | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-36837C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929098 | ||||||
| chr8:96929288
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.850-36647C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929288 | ||||||
| chr8:96929475
|
C | G | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-36460C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929475 | ||||||
| chr8:96929503
|
T | C | 32 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(29): Show | 32 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.850-36432T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929503 | ||||||
| chr8:96929509
|
A | G | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-36426A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929509 | ||||||
| chr8:96929844
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-36091A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96929844 | ||||||
| chr8:96929955
|
T | TA | 2 | a0001c0001t0001g0026a0001c0002t0001g0111 | 2 | HG00099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.850-35979dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96929955 | |||||
| chr8:96930002
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-35933G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96930002 | ||||||
| chr8:96930068
|
A | G | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-35867A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96930068 | ||||||
| chr8:96930389
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.850-35546T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96930389 | ||||||
| chr8:96930636
|
C | T | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.850-35299C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96930636 | ||||||
| chr8:96930742
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-35193T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96930742 | ||||||
| chr8:96931002
|
T | C | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-34933T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931002 | ||||||
| chr8:96931017
|
C | A | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-34918C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931017 | ||||||
| chr8:96931083
|
A | G | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-34852A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931083 | ||||||
| chr8:96931095
|
A | G | 30 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-34840A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931095 | ||||||
| chr8:96931358
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-34577G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931358 | ||||||
| chr8:96931370
|
C | T | 30 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-34565C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931370 | ||||||
| chr8:96931372
|
T | C | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-34563T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931372 | ||||||
| chr8:96931434
|
G | GT | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-34494dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96931434 | |||||
| chr8:96931607
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.850-34328T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931607 | ||||||
| chr8:96931704
|
T | C | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-34231T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931704 | ||||||
| chr8:96931746
|
T | C | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-34189T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931746 | ||||||
| chr8:96931905
|
A | G | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(96): Show | 99 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(96): Show |
intron_variant | MODIFIER | c.850-34030A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96931905 | ||||||
| chr8:96931955
|
AG | A | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-33977delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96931955 | |||||
| chr8:96932175
|
A | AAAGG | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-33737_850-3373 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96932175 | |||||
| chr8:96932332
|
G | A | 29 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0002t0001g0002others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-33603G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96932332 | ||||||
| chr8:96932404
|
C | G | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-33531C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96932404 | ||||||
| chr8:96932468
|
A | G | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(38): Show | 41 | HG00099.hp1 HG01081.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.850-33467A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96932468 | ||||||
| chr8:96932513
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.850-33422C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96932513 | ||||||
| chr8:96932639
|
C | T | 1 | a0001c0002t0001g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.850-33296C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96932639 | ||||||
| chr8:96932935
|
T | G | 30 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-33000T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96932935 | ||||||
| chr8:96933167
|
CT | C | 30 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-32764delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96933167 | |||||
| chr8:96933317
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-32618C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96933317 | ||||||
| chr8:96933412
|
A | G | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-32523A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96933412 | ||||||
| chr8:96933516
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-32419T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96933516 | ||||||
| chr8:96933821
|
AATGGCTT | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-32113_850-3210 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96933821 | ||||||
| chr8:96933941
|
C | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-31994C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96933941 | ||||||
| chr8:96934014
|
G | C | 1 | a0003c0005t0001g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850-31921G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934014 | ||||||
| chr8:96934187
|
G | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-31748G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934187 | ||||||
| chr8:96934245
|
A | G | 30 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.850-31690A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934245 | ||||||
| chr8:96934294
|
T | A | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.850-31641T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934294 | ||||||
| chr8:96934320
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.850-31615G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934320 | ||||||
| chr8:96934405
|
G | T | 9 | a0001c0001t0002g0021a0001c0002t0001g0084a0001c0002t0001g0092others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-31530G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934405 | ||||||
| chr8:96934490
|
G | A | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-31445G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934490 | ||||||
| chr8:96934601
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.850-31334G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934601 | ||||||
| chr8:96934946
|
A | G | 2 | a0001c0001t0002g0020a0005c0013t0001g0043 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.850-30989A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934946 | ||||||
| chr8:96934958
|
T | A | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-30977T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96934958 | ||||||
| chr8:96935098
|
G | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-30837G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96935098 | ||||||
| chr8:96935484
|
G | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(7): Show | 10 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-30451G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96935484 | ||||||
| chr8:96935740
|
G | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-30195G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96935740 | ||||||
| chr8:96935860
|
T | C | 5 | a0001c0001t0001g0033a0001c0002t0001g0071a0001c0002t0001g0072others(2): Show | 5 | NA18747.hp1 NA18962.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-30075T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96935860 | ||||||
| chr8:96936067
|
A | AT | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-29863dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96936067 | |||||
| chr8:96936353
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.850-29582T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96936353 | ||||||
| chr8:96936424
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.850-29511C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96936424 | ||||||
| chr8:96936546
|
A | C | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-29389A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96936546 | ||||||
| chr8:96936833
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850-29102G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96936833 | ||||||
| chr8:96937059
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.850-28876T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96937059 | ||||||
| chr8:96937139
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850-28796C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96937139 | ||||||
| chr8:96937448
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.850-28487G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96937448 | ||||||
| chr8:96937660
|
T | C | 1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-28275T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96937660 | ||||||
| chr8:96937927
|
G | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(82): Show | 85 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.850-28008G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96937927 | ||||||
| chr8:96937955
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850-27980T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96937955 | ||||||
| chr8:96938115
|
C | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-27820C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938115 | ||||||
| chr8:96938254
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(7): Show | 10 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-27681G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938254 | ||||||
| chr8:96938505
|
A | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(82): Show | 85 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.850-27430A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938505 | ||||||
| chr8:96938530
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.850-27405C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938530 | ||||||
| chr8:96938531
|
A | G | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(54): Show | 57 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.850-27404A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938531 | ||||||
| chr8:96938594
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-27341T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938594 | ||||||
| chr8:96938618
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(40): Show | 43 | HG00733.hp2 HG01081.hp2 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.850-27317G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938618 | ||||||
| chr8:96938652
|
G | T | 4 | a0001c0001t0002g0021a0001c0002t0001g0120a0001c0002t0001g0121others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-27283G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938652 | ||||||
| chr8:96938691
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.850-27244C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938691 | ||||||
| chr8:96938754
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-27181T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938754 | ||||||
| chr8:96938757
|
A | C | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.850-27178A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96938757 | ||||||
| chr8:96939044
|
T | A | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850-26891T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96939044 | ||||||
| chr8:96939353
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-26582G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96939353 | ||||||
| chr8:96939849
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-26086G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96939849 | ||||||
| chr8:96939885
|
A | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(82): Show | 85 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.850-26050A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96939885 | ||||||
| chr8:96940009
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-25926C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940009 | ||||||
| chr8:96940060
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850-25875G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940060 | ||||||
| chr8:96940153
|
G | A | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-25782G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940153 | ||||||
| chr8:96940292
|
G | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.850-25643G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940292 | ||||||
| chr8:96940308
|
A | G | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-25627A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940308 | ||||||
| chr8:96940737
|
T | C | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(48): Show | 51 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.850-25198T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940737 | ||||||
| chr8:96940864
|
G | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-25071G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940864 | ||||||
| chr8:96940950
|
C | G | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-24985C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96940950 | ||||||
| chr8:96941535
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.850-24400T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96941535 | ||||||
| chr8:96941823
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-24112C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96941823 | ||||||
| chr8:96942222
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.850-23713A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96942222 | ||||||
| chr8:96942770
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-23165C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96942770 | ||||||
| chr8:96942935
|
C | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-23000C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96942935 | ||||||
| chr8:96943014
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-22921T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96943014 | ||||||
| chr8:96943424
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-22511T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96943424 | ||||||
| chr8:96943728
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-22207T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96943728 | ||||||
| chr8:96943826
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.850-22109C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96943826 | ||||||
| chr8:96944078
|
T | G | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.850-21857T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96944078 | ||||||
| chr8:96944406
|
A | G | 2 | a0001c0002t0002g0085a0002c0003t0001g0008 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.850-21529A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96944406 | ||||||
| chr8:96944515
|
TA | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(17): Show | 20 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.850-21413delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96944515 | |||||
| chr8:96945243
|
G | A | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.850-20692G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96945243 | ||||||
| chr8:96945604
|
G | A | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.850-20331G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96945604 | ||||||
| chr8:96945683
|
TATAAA | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-20247_850-2024 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96945683 | |||||
| chr8:96945943
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0019 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.850-19992A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96945943 | ||||||
| chr8:96945980
|
C | G | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.850-19955C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96945980 | ||||||
| chr8:96946455
|
A | AT | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-19473dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96946455 | |||||
| chr8:96946588
|
T | TC | 11 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0002g0011others(8): Show | 11 | HG01884.hp2 HG01981.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-19341dupC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96946588 | |||||
| chr8:96946959
|
C | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-18976C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96946959 | ||||||
| chr8:96947405
|
CCTA | C | 3 | a0001c0001t0002g0021a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | HG02109.hp1 HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.850-18526_850-1852 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96947405 | |||||
| chr8:96947573
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-18362G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96947573 | ||||||
| chr8:96947797
|
C | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-18138C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96947797 | ||||||
| chr8:96948007
|
C | A | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.850-17928C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96948007 | ||||||
| chr8:96948008
|
A | C | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.850-17927A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96948008 | ||||||
| chr8:96948667
|
T | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-17268T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96948667 | ||||||
| chr8:96948747
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850-17188T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96948747 | ||||||
| chr8:96949019
|
T | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(82): Show | 85 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.850-16916T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96949019 | ||||||
| chr8:96949256
|
ATT | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(58): Show | 61 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.850-16668_850-1666 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96949256 | |||||
| chr8:96949256
|
ATTT | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-16669_850-1666 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96949256 | |||||
| chr8:96949695
|
A | C | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.850-16240A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96949695 | ||||||
| chr8:96949902
|
T | G | 31 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.850-16033T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96949902 | ||||||
| chr8:96949918
|
A | G | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.850-16017A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96949918 | ||||||
| chr8:96950207
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.850-15728T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96950207 | ||||||
| chr8:96950440
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.850-15495A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96950440 | ||||||
| chr8:96951069
|
A | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(3): Show | 6 | HG01081.hp1 NA18747.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-14866A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96951069 | ||||||
| chr8:96951076
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.850-14859A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96951076 | ||||||
| chr8:96951126
|
C | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(25): Show | 28 | HG01081.hp1 HG01884.hp1 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-14809C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96951126 | ||||||
| chr8:96951163
|
A | C | 8 | a0001c0001t0001g0033a0001c0002t0001g0071a0001c0002t0001g0072others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-14772A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96951163 | ||||||
| chr8:96951583
|
T | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-14352T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96951583 | ||||||
| chr8:96951673
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.850-14262G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96951673 | ||||||
| chr8:96951853
|
G | GT | 42 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(39): Show | 42 | HG00099.hp1 HG01081.hp1 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.850-14072dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96951853 | |||||
| chr8:96952351
|
TAA | T | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-13582_850-1358 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96952351 | |||||
| chr8:96952439
|
T | C | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-13496T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96952439 | ||||||
| chr8:96952583
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-13352A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96952583 | ||||||
| chr8:96952627
|
A | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-13308A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96952627 | ||||||
| chr8:96952802
|
TAAA | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-13129_850-1312 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96952802 | |||||
| chr8:96953265
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-12670G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96953265 | ||||||
| chr8:96953362
|
G | A | 1 | a0001c0002t0001g0025 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.850-12573G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96953362 | ||||||
| chr8:96953402
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0002g0067 | 3 | HG01255.hp1 HG01516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.850-12533A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96953402 | ||||||
| chr8:96953560
|
T | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.850-12375T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96953560 | ||||||
| chr8:96953579
|
T | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-12356T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96953579 | ||||||
| chr8:96953710
|
A | G | 1 | a0001c0002t0001g0081 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.850-12225A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96953710 | ||||||
| chr8:96954026
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.850-11909A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954026 | ||||||
| chr8:96954317
|
A | G | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-11618A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954317 | ||||||
| chr8:96954363
|
A | T | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.850-11572A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954363 | ||||||
| chr8:96954483
|
A | T | 7 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0002g0085others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-11452A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954483 | ||||||
| chr8:96954846
|
G | C | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.850-11089G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954846 | ||||||
| chr8:96954986
|
C | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-10949C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954986 | ||||||
| chr8:96954989
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-10946G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96954989 | ||||||
| chr8:96955156
|
C | A | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-10779C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96955156 | ||||||
| chr8:96955233
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-10702C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96955233 | ||||||
| chr8:96956234
|
C | T | 10 | a0001c0001t0002g0044a0001c0002t0001g0005a0001c0002t0001g0006others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-9701C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96956234 | ||||||
| chr8:96956350
|
G | T | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-9585G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96956350 | ||||||
| chr8:96956576
|
A | G | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.850-9359A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96956576 | ||||||
| chr8:96956976
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-8959T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96956976 | ||||||
| chr8:96956979
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-8956A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96956979 | ||||||
| chr8:96957016
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.850-8919A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96957016 | ||||||
| chr8:96957036
|
G | A | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-8899G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96957036 | ||||||
| chr8:96957294
|
A | C | 1 | a0001c0002t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.850-8641A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96957294 | ||||||
| chr8:96957426
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.850-8509T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96957426 | ||||||
| chr8:96957810
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.850-8125A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96957810 | ||||||
| chr8:96957838
|
C | CT | 13 | a0001c0001t0002g0044a0001c0002t0001g0005a0001c0002t0001g0006others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-8085dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96957838 | |||||
| chr8:96957907
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.850-8028C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96957907 | ||||||
| chr8:96958008
|
A | AT | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.850-7916dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96958008 | |||||
| chr8:96958200
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-7735G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958200 | ||||||
| chr8:96958277
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-7658A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958277 | ||||||
| chr8:96958377
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0103 | 3 | HG01975.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.850-7558C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958377 | ||||||
| chr8:96958398
|
T | G | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-7537T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958398 | ||||||
| chr8:96958451
|
T | TAAGAG | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.850-7480_850-7479i others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96958451 | |||||
| chr8:96958655
|
G | A | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.850-7280G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958655 | ||||||
| chr8:96958707
|
T | G | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.850-7228T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958707 | ||||||
| chr8:96958862
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.850-7073T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958862 | ||||||
| chr8:96958891
|
C | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-7044C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958891 | ||||||
| chr8:96958908
|
C | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-7027C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96958908 | ||||||
| chr8:96958912
|
G | GA | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0028others(15): Show | 18 | HG00733.hp2 HG01261.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.850-7008dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96958912 | |||||
| chr8:96958912
|
G | GAA | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(38): Show | 41 | HG00099.hp1 HG01081.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.850-7009_850-7008d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96958912 | |||||
| chr8:96959028
|
A | G | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.850-6907A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959028 | ||||||
| chr8:96959074
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.850-6861C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959074 | ||||||
| chr8:96959410
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-6525G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959410 | ||||||
| chr8:96959794
|
G | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-6141G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959794 | ||||||
| chr8:96959852
|
G | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-6083G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959852 | ||||||
| chr8:96959891
|
C | CA | 32 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(29): Show | 32 | HG01081.hp1 HG01884.hp1 HG01978.hp2 others(29): Show |
intron_variant | MODIFIER | c.850-6025dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96959891 | |||||
| chr8:96959891
|
C | CAA | 6 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0013others(3): Show | 6 | HG03453.hp2 HG03486.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-6026_850-6025d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96959891 | |||||
| chr8:96959891
|
CA | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(32): Show | 35 | HG00733.hp2 HG01081.hp2 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-6025delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96959891 | |||||
| chr8:96959910
|
A | C | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.850-6025A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959910 | ||||||
| chr8:96959913
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-6022A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96959913 | ||||||
| chr8:96960003
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.850-5932T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96960003 | ||||||
| chr8:96960114
|
G | A | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.850-5821G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96960114 | ||||||
| chr8:96960336
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.850-5599T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96960336 | ||||||
| chr8:96960793
|
ATCT | A | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.850-5138_850-5136d others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96960793 | |||||
| chr8:96961195
|
C | G | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.850-4740C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96961195 | ||||||
| chr8:96961970
|
A | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-3965A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96961970 | ||||||
| chr8:96962054
|
C | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-3881C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96962054 | ||||||
| chr8:96962331
|
G | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.850-3604G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96962331 | ||||||
| chr8:96962407
|
G | T | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-3528G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96962407 | ||||||
| chr8:96962515
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-3420G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96962515 | ||||||
| chr8:96962687
|
T | G | 1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850-3248T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96962687 | ||||||
| chr8:96962821
|
G | A | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-3114G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96962821 | ||||||
| chr8:96962894
|
GT | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(9): Show | 12 | HG01884.hp1 HG02004.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.850-3032delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96962894 | |||||
| chr8:96963003
|
C | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-2932C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963003 | ||||||
| chr8:96963026
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-2909A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963026 | ||||||
| chr8:96963357
|
A | T | 34 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(31): Show | 34 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.850-2578A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963357 | ||||||
| chr8:96963432
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.850-2503G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963432 | ||||||
| chr8:96963460
|
G | A | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.850-2475G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963460 | ||||||
| chr8:96963667
|
C | T | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.850-2268C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963667 | ||||||
| chr8:96963689
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850-2246G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963689 | ||||||
| chr8:96963770
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850-2165T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96963770 | ||||||
| chr8:96964075
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.850-1860T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96964075 | ||||||
| chr8:96964084
|
TTTTC | T | 2 | a0001c0002t0001g0123a0001c0007t0001g0038 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.850-1843_850-1840d others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964084 | |||||
| chr8:96964088
|
CTTTCT | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-1843_850-1839d others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964088 | |||||
| chr8:96964092
|
C | CT | 36 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(33): Show | 36 | HG00099.hp1 HG01081.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.850-1830dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964092 | |||||
| chr8:96964173
|
T | TAC | 9 | a0001c0001t0001g0017a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-1718_850-1717d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
T | TACAC | 13 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(10): Show | 13 | HG00733.hp2 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.850-1720_850-1717d others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
T | TACACAC | 11 | a0001c0001t0002g0021a0001c0002t0001g0049a0001c0002t0001g0058others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-1722_850-1717d others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
T | TACACACA others(3): Show |
1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.850-1726_850-1717d others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
TAC | T | 14 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(11): Show | 14 | HG01081.hp1 HG01255.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.850-1718_850-1717d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
TACAC | T | 52 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(49): Show | 52 | HG00099.hp1 HG00733.hp1 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.850-1720_850-1717d others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
TACACAC | T | 7 | a0001c0001t0001g0028a0001c0001t0004g0083a0001c0002t0001g0005others(4): Show | 7 | HG02280.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-1722_850-1717d others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
TACACACA others(1): Show |
T | 3 | a0003c0005t0001g0007a0003c0005t0001g0068a0008c0011t0002g0037 | 3 | HG02622.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.850-1724_850-1717d others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964173
|
TACACACA others(13): Show |
T | 4 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(1): Show | 4 | HG00099.hp2 HG04184.hp2 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-1736_850-1717d others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96964173 | |||||
| chr8:96964179
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.850-1756C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96964179 | ||||||
| chr8:96964314
|
T | C | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.850-1621T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96964314 | ||||||
| chr8:96964558
|
C | T | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.850-1377C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96964558 | ||||||
| chr8:96965372
|
CT | C | 111 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(108): Show |
intron_variant | MODIFIER | c.850-544delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 96965372 | |||||
| chr8:96965418
|
G | A | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-517G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96965418 | ||||||
| chr8:96965621
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.850-314G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96965621 | ||||||
| chr8:96965658
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-277C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 4/7 | chr8 | 96965658 | ||||||
| chr8:96966077
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0125a0001c0001t0002g0022 | 3 | HG01884.hp1 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.961+31G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96966077 | ||||||
| chr8:96966193
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+147T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96966193 | ||||||
| chr8:96966987
|
T | G | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.961+941T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96966987 | ||||||
| chr8:96967158
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.961+1112A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96967158 | ||||||
| chr8:96967242
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.961+1196T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96967242 | ||||||
| chr8:96967493
|
G | T | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.961+1447G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96967493 | ||||||
| chr8:96967932
|
T | A | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.961+1886T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96967932 | ||||||
| chr8:96967933
|
A | T | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.961+1887A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96967933 | ||||||
| chr8:96968049
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.961+2003A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968049 | ||||||
| chr8:96968309
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.961+2263G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968309 | ||||||
| chr8:96968507
|
G | T | 1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.961+2461G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968507 | ||||||
| chr8:96968653
|
T | C | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+2607T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968653 | ||||||
| chr8:96968762
|
G | C | 1 | a0001c0002t0001g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.961+2716G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968762 | ||||||
| chr8:96968774
|
C | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.961+2728C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968774 | ||||||
| chr8:96968881
|
C | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.961+2835C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96968881 | ||||||
| chr8:96969290
|
G | A | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.961+3244G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96969290 | ||||||
| chr8:96969445
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961+3399A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96969445 | ||||||
| chr8:96969488
|
TA | T | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.961+3445delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96969488 | |||||
| chr8:96969508
|
G | C | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+3462G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96969508 | ||||||
| chr8:96969625
|
C | T | 1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.961+3579C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96969625 | ||||||
| chr8:96970565
|
C | CT | 5 | a0001c0001t0001g0056a0001c0002t0001g0025a0001c0002t0001g0115others(2): Show | 5 | HG01978.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+4535dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96970565 | |||||
| chr8:96970628
|
A | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.961+4582A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96970628 | ||||||
| chr8:96970708
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+4662C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96970708 | ||||||
| chr8:96970744
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.961+4698T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96970744 | ||||||
| chr8:96970843
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0020others(1): Show | 4 | HG02886.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.961+4797G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96970843 | ||||||
| chr8:96970853
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0002g0020others(1): Show | 4 | HG02886.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.961+4807G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96970853 | ||||||
| chr8:96971092
|
C | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+5046C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96971092 | ||||||
| chr8:96971384
|
C | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.961+5338C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96971384 | ||||||
| chr8:96971674
|
G | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.961+5628G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96971674 | ||||||
| chr8:96971831
|
G | A | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+5785G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96971831 | ||||||
| chr8:96971912
|
G | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.961+5866G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96971912 | ||||||
| chr8:96971922
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.961+5876A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96971922 | ||||||
| chr8:96972000
|
C | A | 1 | a0001c0002t0001g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.961+5954C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972000 | ||||||
| chr8:96972030
|
A | G | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.961+5984A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972030 | ||||||
| chr8:96972181
|
C | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+6135C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972181 | ||||||
| chr8:96972226
|
G | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+6180G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972226 | ||||||
| chr8:96972628
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.961+6582G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972628 | ||||||
| chr8:96972658
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.961+6612C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972658 | ||||||
| chr8:96972726
|
T | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.961+6680T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972726 | ||||||
| chr8:96972873
|
G | C | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.961+6827G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96972873 | ||||||
| chr8:96973013
|
C | A | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.961+6967C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973013 | ||||||
| chr8:96973014
|
A | G | 39 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0047others(36): Show | 39 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.961+6968A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973014 | ||||||
| chr8:96973047
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+7001G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973047 | ||||||
| chr8:96973162
|
T | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+7116T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973162 | ||||||
| chr8:96973440
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.961+7394A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973440 | ||||||
| chr8:96973493
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+7447C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973493 | ||||||
| chr8:96973779
|
T | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(11): Show | 14 | HG01884.hp1 HG02004.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.961+7733T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96973779 | ||||||
| chr8:96974075
|
G | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0108 | 3 | HG02040.hp2 NA19005.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.961+8029G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974075 | ||||||
| chr8:96974177
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.961+8131G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974177 | ||||||
| chr8:96974232
|
G | GA | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+8192dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96974232 | |||||
| chr8:96974391
|
A | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.961+8345A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974391 | ||||||
| chr8:96974800
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.961+8754A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974800 | ||||||
| chr8:96974829
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.961+8783C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974829 | ||||||
| chr8:96974876
|
G | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+8830G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974876 | ||||||
| chr8:96974889
|
A | T | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.961+8843A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974889 | ||||||
| chr8:96974974
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(17): Show | 20 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.961+8928C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96974974 | ||||||
| chr8:96975080
|
A | G | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.961+9034A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96975080 | ||||||
| chr8:96975311
|
G | GAACAGAC others(4): Show |
89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.961+9270_961+9271i others(13): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96975311 | |||||
| chr8:96975384
|
T | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(17): Show | 20 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.961+9338T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96975384 | ||||||
| chr8:96975522
|
C | CA | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.961+9486dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96975522 | |||||
| chr8:96975531
|
A | G | 4 | a0001c0001t0001g0028a0001c0002t0001g0115a0001c0002t0002g0004others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+9485A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96975531 | ||||||
| chr8:96975941
|
C | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(37): Show | 40 | HG00099.hp1 HG01081.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.961+9895C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96975941 | ||||||
| chr8:96975959
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.961+9913A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96975959 | ||||||
| chr8:96975986
|
T | C | 115 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.961+9940T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96975986 | ||||||
| chr8:96976247
|
C | CA | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0077others(5): Show | 8 | HG00099.hp1 HG01517.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+10226dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96976247 | |||||
| chr8:96976247
|
CA | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(30): Show | 33 | HG00733.hp1 HG01081.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.961+10226delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96976247 | |||||
| chr8:96976247
|
CAA | C | 27 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0047others(24): Show | 27 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.961+10225_961+1022 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96976247 | |||||
| chr8:96976247
|
CAAA | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(23): Show | 26 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.961+10224_961+1022 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96976247 | |||||
| chr8:96976247
|
CAAAA | C | 8 | a0001c0001t0002g0021a0001c0002t0001g0018a0001c0002t0001g0092others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+10223_961+1022 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96976247 | |||||
| chr8:96976247
|
CAAAAA | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.961+10222_961+1022 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96976247 | |||||
| chr8:96976340
|
A | G | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.961+10294A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96976340 | ||||||
| chr8:96976452
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+10406A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96976452 | ||||||
| chr8:96976532
|
G | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.961+10486G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96976532 | ||||||
| chr8:96976667
|
A | G | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+10621A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96976667 | ||||||
| chr8:96977324
|
CA | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(75): Show | 78 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.961+11293delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96977324 | |||||
| chr8:96977324
|
CAA | C | 5 | a0001c0001t0001g0028a0001c0002t0001g0084a0003c0005t0001g0007others(2): Show | 5 | HG02622.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.961+11292_961+1129 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96977324 | |||||
| chr8:96977983
|
A | T | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.961+11937A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96977983 | ||||||
| chr8:96977990
|
A | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.961+11944A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96977990 | ||||||
| chr8:96977998
|
T | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+11952T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96977998 | ||||||
| chr8:96978085
|
ATCT | A | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.961+12043_961+1204 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96978085 | |||||
| chr8:96978526
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+12480G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96978526 | ||||||
| chr8:96978541
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.961+12495A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96978541 | ||||||
| chr8:96979050
|
T | TA | 38 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(35): Show | 38 | HG00099.hp1 HG01261.hp1 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.961+13016dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96979050 | |||||
| chr8:96979050
|
T | TAA | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(2): Show | 5 | HG01081.hp1 NA18747.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.961+13015_961+1301 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96979050 | |||||
| chr8:96979050
|
TA | T | 33 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0002g0021others(30): Show | 33 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.961+13016delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96979050 | |||||
| chr8:96979157
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+13111C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96979157 | ||||||
| chr8:96979573
|
A | G | 6 | a0001c0002t0001g0086a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | NA18979.hp1 NA18990.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.961+13527A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96979573 | ||||||
| chr8:96979690
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.961+13644A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96979690 | ||||||
| chr8:96979851
|
G | A | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+13805G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96979851 | ||||||
| chr8:96979909
|
G | A | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.961+13863G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96979909 | ||||||
| chr8:96980061
|
A | G | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.961+14015A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96980061 | ||||||
| chr8:96980779
|
G | C | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.961+14733G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96980779 | ||||||
| chr8:96980813
|
G | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961+14767G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96980813 | ||||||
| chr8:96981099
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+15053A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96981099 | ||||||
| chr8:96981289
|
C | A | 3 | a0001c0002t0001g0115a0001c0002t0002g0004a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.961+15243C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96981289 | ||||||
| chr8:96981540
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.961+15494G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96981540 | ||||||
| chr8:96981717
|
T | C | 2 | a0001c0002t0001g0055a0001c0002t0001g0059 | 2 | HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.961+15671T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96981717 | ||||||
| chr8:96982145
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.961+16099T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96982145 | ||||||
| chr8:96982446
|
C | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.961+16400C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96982446 | ||||||
| chr8:96983192
|
C | G | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.961+17146C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96983192 | ||||||
| chr8:96983430
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.961+17384G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96983430 | ||||||
| chr8:96983705
|
G | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(20): Show | 23 | HG01081.hp1 HG02004.hp1 HG02273.hp2 others(20): Show |
intron_variant | MODIFIER | c.961+17659G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96983705 | ||||||
| chr8:96983828
|
CT | C | 7 | a0001c0001t0001g0014a0001c0002t0001g0071a0001c0002t0001g0072others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.961+17796delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96983828 | |||||
| chr8:96984188
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+18142A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96984188 | ||||||
| chr8:96984361
|
G | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0021others(24): Show | 27 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.961+18315G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96984361 | ||||||
| chr8:96984930
|
C | T | 10 | a0001c0001t0002g0044a0001c0002t0001g0005a0001c0002t0001g0006others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.961+18884C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96984930 | ||||||
| chr8:96985014
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.961+18968T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96985014 | ||||||
| chr8:96985269
|
GT | G | 55 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(52): Show | 55 | HG00733.hp2 HG01081.hp1 HG01261.hp1 others(52): Show |
intron_variant | MODIFIER | c.961+19234delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96985269 | |||||
| chr8:96985728
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+19682G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96985728 | ||||||
| chr8:96986041
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+19995C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96986041 | ||||||
| chr8:96986350
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.961+20304T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96986350 | ||||||
| chr8:96986514
|
C | A | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.961+20468C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96986514 | ||||||
| chr8:96986909
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.961+20863T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96986909 | ||||||
| chr8:96986924
|
C | A | 1 | a0001c0002t0001g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.961+20878C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96986924 | ||||||
| chr8:96987051
|
G | A | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(39): Show | 42 | HG00733.hp2 HG01081.hp1 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.961+21005G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987051 | ||||||
| chr8:96987096
|
G | A | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.961+21050G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987096 | ||||||
| chr8:96987192
|
T | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(29): Show | 32 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.961+21146T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987192 | ||||||
| chr8:96987297
|
A | G | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.961+21251A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987297 | ||||||
| chr8:96987396
|
A | G | 2 | a0001c0002t0001g0091a0001c0004t0001g0114 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.961+21350A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987396 | ||||||
| chr8:96987429
|
A | G | 4 | a0001c0001t0001g0014a0001c0002t0001g0115a0001c0002t0002g0004others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+21383A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987429 | ||||||
| chr8:96987513
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.961+21467A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987513 | ||||||
| chr8:96987603
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.961+21557C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987603 | ||||||
| chr8:96987923
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.961+21877C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96987923 | ||||||
| chr8:96988029
|
C | A | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.961+21983C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96988029 | ||||||
| chr8:96988196
|
C | A | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.961+22150C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96988196 | ||||||
| chr8:96988799
|
G | A | 115 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.961+22753G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96988799 | ||||||
| chr8:96988807
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+22761T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96988807 | ||||||
| chr8:96989282
|
A | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.961+23236A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96989282 | ||||||
| chr8:96989362
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+23316A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96989362 | ||||||
| chr8:96989466
|
C | T | 25 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(22): Show | 25 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.961+23420C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96989466 | ||||||
| chr8:96989539
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.961+23493G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96989539 | ||||||
| chr8:96990009
|
A | C | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.961+23963A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990009 | ||||||
| chr8:96990053
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.961+24007A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990053 | ||||||
| chr8:96990109
|
G | A | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+24063G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990109 | ||||||
| chr8:96990319
|
T | G | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+24273T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990319 | ||||||
| chr8:96990632
|
T | G | 1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.961+24586T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990632 | ||||||
| chr8:96990653
|
A | G | 1 | a0001c0002t0002g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.961+24607A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990653 | ||||||
| chr8:96990819
|
T | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0027others(32): Show | 35 | HG01081.hp1 HG01261.hp1 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.961+24773T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990819 | ||||||
| chr8:96990887
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.961+24841C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990887 | ||||||
| chr8:96990971
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.961+24925A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96990971 | ||||||
| chr8:96991323
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.961+25277G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96991323 | ||||||
| chr8:96991430
|
C | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+25384C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96991430 | ||||||
| chr8:96991551
|
GTCATAAT others(5): Show |
G | 3 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068 | 3 | HG02622.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.961+25507_961+2551 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991551 | |||||
| chr8:96991553
|
CATA | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0002g0100others(6): Show | 9 | HG00099.hp1 HG01516.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.961+25555_961+2555 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991553 | |||||
| chr8:96991553
|
CATAATA | C | 17 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0002t0001g0002others(14): Show | 17 | HG01516.hp1 HG01517.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.961+25552_961+2555 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991553 | |||||
| chr8:96991553
|
CATAATAA others(2): Show |
C | 37 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(34): Show | 37 | HG00099.hp2 HG00733.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.961+25549_961+2555 others(13): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991553 | |||||
| chr8:96991553
|
CATAATAA others(5): Show |
C | 15 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0061others(12): Show | 15 | HG01261.hp1 HG01261.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.961+25546_961+2555 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991553 | |||||
| chr8:96991553
|
CATAATAA others(8): Show |
C | 4 | a0001c0001t0001g0036a0001c0001t0001g0046a0001c0002t0002g0004others(1): Show | 4 | HG02257.hp2 HG02273.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+25543_961+2555 others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991553 | |||||
| chr8:96991553
|
CATAATAA others(11): Show |
C | 23 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(20): Show | 23 | HG01081.hp1 HG02004.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.961+25540_961+2555 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96991553 | |||||
| chr8:96991877
|
T | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(40): Show | 43 | HG00733.hp2 HG01081.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.961+25831T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96991877 | ||||||
| chr8:96992132
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.961+26086T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96992132 | ||||||
| chr8:96992267
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+26221G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96992267 | ||||||
| chr8:96992503
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961+26457T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96992503 | ||||||
| chr8:96992639
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.961+26593G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96992639 | ||||||
| chr8:96992934
|
C | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.961+26888C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96992934 | ||||||
| chr8:96992999
|
A | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.961+26953A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96992999 | ||||||
| chr8:96993174
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0002g0050 | 2 | HG01261.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.961+27128G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96993174 | ||||||
| chr8:96993575
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(7): Show | 10 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.961+27529T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96993575 | ||||||
| chr8:96994111
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.961+28065G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96994111 | ||||||
| chr8:96994275
|
G | A | 2 | a0001c0002t0001g0018a0001c0002t0001g0040 | 2 | HG01261.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.961+28229G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96994275 | ||||||
| chr8:96994330
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.961+28284A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96994330 | ||||||
| chr8:96994821
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.961+28775C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96994821 | ||||||
| chr8:96995583
|
AAGGTCTG others(5): Show |
A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.961+29540_961+2955 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96995583 | |||||
| chr8:96995589
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+29543T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96995589 | ||||||
| chr8:96995670
|
A | T | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(79): Show | 82 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.961+29624A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96995670 | ||||||
| chr8:96995671
|
A | T | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.961+29625A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96995671 | ||||||
| chr8:96995684
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.961+29638T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96995684 | ||||||
| chr8:96996150
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+30104T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96996150 | ||||||
| chr8:96996520
|
G | T | 5 | a0001c0001t0001g0014a0001c0002t0001g0084a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+30474G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96996520 | ||||||
| chr8:96996791
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(81): Show | 84 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(81): Show |
intron_variant | MODIFIER | c.961+30745C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96996791 | ||||||
| chr8:96996890
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.961+30844T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96996890 | ||||||
| chr8:96996963
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.961+30917A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96996963 | ||||||
| chr8:96997135
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.961+31089A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96997135 | ||||||
| chr8:96997270
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.961+31224G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96997270 | ||||||
| chr8:96997578
|
A | G | 3 | a0001c0002t0001g0123a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.961+31532A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96997578 | ||||||
| chr8:96998225
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-31178G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96998225 | ||||||
| chr8:96998390
|
A | G | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.962-31013A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96998390 | ||||||
| chr8:96998445
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-30958G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96998445 | ||||||
| chr8:96998862
|
G | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-30541G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96998862 | ||||||
| chr8:96999115
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-30288C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96999115 | ||||||
| chr8:96999230
|
C | CT | 5 | a0001c0001t0001g0047a0001c0002t0001g0091a0001c0004t0001g0107others(2): Show | 5 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-30160dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 96999230 | |||||
| chr8:96999392
|
G | A | 5 | a0001c0001t0001g0047a0001c0002t0001g0091a0001c0004t0001g0107others(2): Show | 5 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-30011G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96999392 | ||||||
| chr8:96999456
|
A | G | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-29947A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96999456 | ||||||
| chr8:96999563
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.962-29840C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96999563 | ||||||
| chr8:96999772
|
T | G | 4 | a0001c0001t0002g0067a0001c0002t0001g0081a0001c0002t0002g0082others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-29631T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 96999772 | ||||||
| chr8:97000419
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.962-28984C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97000419 | ||||||
| chr8:97001276
|
G | A | 25 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(22): Show | 25 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.962-28127G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97001276 | ||||||
| chr8:97001456
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.962-27947G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97001456 | ||||||
| chr8:97001624
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.962-27779C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97001624 | ||||||
| chr8:97001721
|
C | CT | 6 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-27659dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97001721 | |||||
| chr8:97001721
|
CT | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0002g0100others(4): Show | 7 | HG01943.hp1 HG01975.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.962-27659delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97001721 | |||||
| chr8:97001721
|
CTT | C | 62 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 62 | HG01081.hp1 HG01081.hp2 HG01261.hp1 others(59): Show |
intron_variant | MODIFIER | c.962-27660_962-2765 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97001721 | |||||
| chr8:97002021
|
T | C | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(81): Show | 84 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(81): Show |
intron_variant | MODIFIER | c.962-27382T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97002021 | ||||||
| chr8:97002050
|
G | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | NA18747.hp1 NA18945.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.962-27353G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97002050 | ||||||
| chr8:97002122
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-27281C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97002122 | ||||||
| chr8:97002959
|
T | C | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(44): Show | 47 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.962-26444T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97002959 | ||||||
| chr8:97003364
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.962-26039T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97003364 | ||||||
| chr8:97003438
|
CTT | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-25963_962-2596 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97003438 | |||||
| chr8:97003767
|
G | T | 8 | a0001c0002t0001g0025a0001c0002t0001g0055a0001c0002t0001g0059others(5): Show | 8 | HG00099.hp1 HG01261.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.962-25636G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97003767 | ||||||
| chr8:97004360
|
G | C | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(44): Show | 47 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.962-25043G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97004360 | ||||||
| chr8:97004692
|
A | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(36): Show | 39 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.962-24711A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97004692 | ||||||
| chr8:97004750
|
T | C | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-24653T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97004750 | ||||||
| chr8:97004791
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-24612G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97004791 | ||||||
| chr8:97005486
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(6): Show | 9 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.962-23917G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97005486 | ||||||
| chr8:97005500
|
G | A | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.962-23903G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97005500 | ||||||
| chr8:97005533
|
C | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-23870C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97005533 | ||||||
| chr8:97005645
|
A | C | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.962-23758A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97005645 | ||||||
| chr8:97005761
|
G | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.962-23642G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97005761 | ||||||
| chr8:97005802
|
G | C | 3 | a0001c0002t0001g0084a0001c0002t0001g0115a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.962-23601G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97005802 | ||||||
| chr8:97006036
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0077others(7): Show | 10 | HG01261.hp1 HG01517.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.962-23367G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97006036 | ||||||
| chr8:97006156
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-23247T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97006156 | ||||||
| chr8:97006350
|
C | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-23053C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97006350 | ||||||
| chr8:97006477
|
A | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-22926A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97006477 | ||||||
| chr8:97006606
|
A | G | 40 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(37): Show | 40 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(37): Show |
intron_variant | MODIFIER | c.962-22797A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97006606 | ||||||
| chr8:97007236
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.962-22167A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97007236 | ||||||
| chr8:97007524
|
A | G | 2 | a0001c0001t0001g0026a0001c0002t0001g0111 | 2 | HG00099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.962-21879A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97007524 | ||||||
| chr8:97007910
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-21493C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97007910 | ||||||
| chr8:97008052
|
G | A | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.962-21351G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97008052 | ||||||
| chr8:97008139
|
TA | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.962-21253delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97008139 | |||||
| chr8:97008234
|
C | A | 3 | a0001c0002t0001g0084a0001c0002t0001g0115a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.962-21169C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97008234 | ||||||
| chr8:97008768
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-20635T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97008768 | ||||||
| chr8:97008884
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.962-20519G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97008884 | ||||||
| chr8:97009634
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-19769G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97009634 | ||||||
| chr8:97009735
|
A | C | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-19668A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97009735 | ||||||
| chr8:97009960
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.962-19443C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97009960 | ||||||
| chr8:97010201
|
C | A | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.962-19202C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97010201 | ||||||
| chr8:97010204
|
C | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(44): Show | 47 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.962-19199C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97010204 | ||||||
| chr8:97011236
|
A | G | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.962-18167A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011236 | ||||||
| chr8:97011484
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.962-17919T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011484 | ||||||
| chr8:97011741
|
C | A | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.962-17662C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011741 | ||||||
| chr8:97011781
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(32): Show | 35 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.962-17622T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011781 | ||||||
| chr8:97011806
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.962-17597C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011806 | ||||||
| chr8:97011888
|
T | C | 3 | a0001c0002t0001g0081a0001c0002t0002g0082a0007c0009t0001g0062 | 3 | HG00099.hp1 HG01943.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.962-17515T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011888 | ||||||
| chr8:97011944
|
C | T | 3 | a0001c0002t0001g0084a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | HG02970.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-17459C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011944 | ||||||
| chr8:97011974
|
T | A | 2 | a0002c0003t0001g0015a0004c0006t0001g0074 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.962-17429T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97011974 | ||||||
| chr8:97012067
|
C | G | 5 | a0001c0001t0001g0014a0001c0002t0001g0084a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.962-17336C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97012067 | ||||||
| chr8:97012257
|
A | G | 5 | a0001c0001t0001g0014a0001c0002t0001g0084a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.962-17146A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97012257 | ||||||
| chr8:97012434
|
T | C | 5 | a0001c0001t0001g0047a0001c0002t0001g0091a0001c0004t0001g0107others(2): Show | 5 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-16969T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97012434 | ||||||
| chr8:97012713
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0019a0005c0013t0001g0043 | 3 | HG02886.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.962-16690C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97012713 | ||||||
| chr8:97013027
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(45): Show | 48 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.962-16376G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013027 | ||||||
| chr8:97013164
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.962-16239C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013164 | ||||||
| chr8:97013229
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(45): Show | 48 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.962-16174G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013229 | ||||||
| chr8:97013390
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-16013G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013390 | ||||||
| chr8:97013426
|
A | G | 6 | a0001c0002t0001g0086a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | NA18979.hp1 NA18990.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-15977A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013426 | ||||||
| chr8:97013457
|
A | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.962-15946A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013457 | ||||||
| chr8:97013627
|
A | G | 11 | a0001c0002t0001g0049a0001c0002t0001g0058a0001c0002t0001g0065others(8): Show | 11 | NA18945.hp1 NA18979.hp1 NA18990.hp1 others(8): Show |
intron_variant | MODIFIER | c.962-15776A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013627 | ||||||
| chr8:97013631
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.962-15772C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013631 | ||||||
| chr8:97013638
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.962-15765C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97013638 | ||||||
| chr8:97014080
|
A | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.962-15323A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014080 | ||||||
| chr8:97014140
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.962-15263G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014140 | ||||||
| chr8:97014272
|
T | C | 1 | a0001c0002t0002g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.962-15131T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014272 | ||||||
| chr8:97014421
|
C | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-14982C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014421 | ||||||
| chr8:97014544
|
A | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-14859A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014544 | ||||||
| chr8:97014669
|
C | A | 5 | a0001c0001t0001g0033a0001c0002t0001g0071a0001c0002t0001g0072others(2): Show | 5 | NA18747.hp1 NA18962.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-14734C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014669 | ||||||
| chr8:97014900
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.962-14503C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014900 | ||||||
| chr8:97014943
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.962-14460G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97014943 | ||||||
| chr8:97015077
|
A | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.962-14326A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97015077 | ||||||
| chr8:97015202
|
G | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0055a0001c0002t0002g0050others(1): Show | 4 | HG01261.hp1 HG01978.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-14201G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97015202 | ||||||
| chr8:97015510
|
T | C | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.962-13893T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97015510 | ||||||
| chr8:97015768
|
C | G | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.962-13635C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97015768 | ||||||
| chr8:97015880
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-13523A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97015880 | ||||||
| chr8:97016093
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.962-13310A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97016093 | ||||||
| chr8:97016240
|
G | T | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.962-13163G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97016240 | ||||||
| chr8:97016275
|
G | A | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.962-13128G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97016275 | ||||||
| chr8:97016664
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-12739T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97016664 | ||||||
| chr8:97016961
|
C | CTT | 4 | a0001c0001t0001g0014a0001c0002t0001g0115a0001c0002t0002g0004others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-12439_962-1243 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97016961 | |||||
| chr8:97016972
|
C | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.962-12431C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97016972 | ||||||
| chr8:97017082
|
C | A | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-12321C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017082 | ||||||
| chr8:97017521
|
A | C | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.962-11882A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017521 | ||||||
| chr8:97017584
|
A | G | 3 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.962-11819A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017584 | ||||||
| chr8:97017599
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.962-11804G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017599 | ||||||
| chr8:97017869
|
C | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-11534C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017869 | ||||||
| chr8:97017903
|
T | A | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.962-11500T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017903 | ||||||
| chr8:97017934
|
T | C | 125 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(122): Show |
intron_variant | MODIFIER | c.962-11469T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97017934 | ||||||
| chr8:97018026
|
C | A | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.962-11377C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018026 | ||||||
| chr8:97018083
|
T | C | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-11320T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018083 | ||||||
| chr8:97018324
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.962-11079C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018324 | ||||||
| chr8:97018482
|
C | A | 3 | a0001c0002t0001g0084a0001c0002t0001g0115a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.962-10921C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018482 | ||||||
| chr8:97018551
|
A | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-10852A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018551 | ||||||
| chr8:97018561
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-10842G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018561 | ||||||
| chr8:97018886
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-10517T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97018886 | ||||||
| chr8:97019120
|
G | A | 5 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(2): Show | 5 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-10283G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019120 | ||||||
| chr8:97019273
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.962-10130C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019273 | ||||||
| chr8:97019522
|
G | T | 3 | a0001c0002t0001g0084a0001c0002t0001g0115a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.962-9881G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019522 | ||||||
| chr8:97019554
|
T | C | 5 | a0001c0001t0001g0047a0001c0002t0001g0091a0001c0004t0001g0107others(2): Show | 5 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-9849T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019554 | ||||||
| chr8:97019583
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-9820A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019583 | ||||||
| chr8:97019583
|
A | T | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.962-9820A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019583 | ||||||
| chr8:97019837
|
G | C | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-9566G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019837 | ||||||
| chr8:97019922
|
CAT | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-9478_962-9477d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97019922 | |||||
| chr8:97019990
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(32): Show | 35 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.962-9413T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97019990 | ||||||
| chr8:97020058
|
A | G | 1 | a0001c0002t0001g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.962-9345A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020058 | ||||||
| chr8:97020071
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.962-9332G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020071 | ||||||
| chr8:97020140
|
T | C | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.962-9263T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020140 | ||||||
| chr8:97020141
|
T | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.962-9262T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020141 | ||||||
| chr8:97020213
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-9190G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020213 | ||||||
| chr8:97020227
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.962-9176C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020227 | ||||||
| chr8:97020339
|
C | G | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-9064C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020339 | ||||||
| chr8:97020565
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.962-8838G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97020565 | ||||||
| chr8:97021052
|
G | A | 5 | a0001c0001t0001g0014a0001c0002t0001g0084a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.962-8351G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021052 | ||||||
| chr8:97021125
|
A | G | 1 | a0002c0003t0001g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.962-8278A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021125 | ||||||
| chr8:97021166
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.962-8237C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021166 | ||||||
| chr8:97021183
|
T | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-8220T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021183 | ||||||
| chr8:97021303
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-8100G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021303 | ||||||
| chr8:97021462
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-7941A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021462 | ||||||
| chr8:97021566
|
T | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.962-7837T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021566 | ||||||
| chr8:97021579
|
A | G | 1 | a0001c0002t0001g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.962-7824A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021579 | ||||||
| chr8:97021654
|
A | C | 28 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.962-7749A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021654 | ||||||
| chr8:97021676
|
A | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-7727A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97021676 | ||||||
| chr8:97022142
|
C | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-7261C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022142 | ||||||
| chr8:97022411
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-6992C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022411 | ||||||
| chr8:97022441
|
C | G | 5 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-6962C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022441 | ||||||
| chr8:97022489
|
A | G | 4 | a0001c0001t0001g0014a0001c0002t0001g0115a0001c0002t0002g0004others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-6914A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022489 | ||||||
| chr8:97022874
|
A | G | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.962-6529A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022874 | ||||||
| chr8:97022965
|
A | ATATATAT others(26): Show |
9 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0080others(6): Show | 9 | HG01975.hp2 HG01981.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.962-6425_962-6393d others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97022965 | |||||
| chr8:97022976
|
CTGTATAT others(6): Show |
C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-6425_962-6413d others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97022976 | |||||
| chr8:97022978
|
G | GTATACAG others(26): Show |
1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.962-6421_962-6420i others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97022978 | |||||
| chr8:97022978
|
G | GTATATAG others(26): Show |
1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.962-6396_962-6364d others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97022978 | |||||
| chr8:97022978
|
G | GTATATAG others(26): Show |
2 | a0001c0002t0002g0085a0002c0003t0001g0008 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.962-6407_962-6406i others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97022978 | |||||
| chr8:97022981
|
T | TATAGTAT others(8): Show |
1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.962-6420_962-6406d others(17): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97022981 | |||||
| chr8:97022996
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-6407C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022996 | ||||||
| chr8:97022997
|
AGTATATA others(47): Show |
A | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.962-6405_962-6352d others(56): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97022997 | ||||||
| chr8:97023011
|
A | G | 1 | a0001c0002t0001g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.962-6392A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023011 | ||||||
| chr8:97023016
|
T | C | 14 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0080others(11): Show | 14 | HG01884.hp2 HG01975.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.962-6387T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023016 | ||||||
| chr8:97023016
|
T | TAGTATAT others(26): Show |
31 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.962-6364_962-6363i others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023016 | |||||
| chr8:97023016
|
T | TAGTATAT others(26): Show |
2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.962-6374_962-6373i others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023016 | |||||
| chr8:97023020
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.962-6362_962-6352d others(13): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023020 | |||||
| chr8:97023030
|
A | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6373A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023030 | ||||||
| chr8:97023031
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6372G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023031 | ||||||
| chr8:97023033
|
A | ATATATAT others(2): Show |
2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6364_962-6363i others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023033 | |||||
| chr8:97023042
|
G | GTA | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6354_962-6353d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023042 | |||||
| chr8:97023052
|
T | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6351T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023052 | ||||||
| chr8:97023053
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.962-6350G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023053 | ||||||
| chr8:97023057
|
A | ATATACTG | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6342_962-6341i others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023057 | |||||
| chr8:97023062
|
G | T | 3 | a0001c0001t0001g0077a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA18979.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6341G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023062 | ||||||
| chr8:97023112
|
C | CTA | 43 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.962-6280_962-6279d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 97023112 | |||||
| chr8:97023380
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-6023C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023380 | ||||||
| chr8:97023687
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.962-5716C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023687 | ||||||
| chr8:97023758
|
A | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.962-5645A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023758 | ||||||
| chr8:97023895
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-5508C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97023895 | ||||||
| chr8:97024632
|
G | A | 2 | a0001c0001t0001g0014a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.962-4771G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97024632 | ||||||
| chr8:97025495
|
C | T | 26 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(23): Show | 26 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.962-3908C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97025495 | ||||||
| chr8:97025855
|
C | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(37): Show | 40 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(37): Show |
intron_variant | MODIFIER | c.962-3548C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97025855 | ||||||
| chr8:97026240
|
A | G | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.962-3163A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026240 | ||||||
| chr8:97026446
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-2957G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026446 | ||||||
| chr8:97026509
|
T | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-2894T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026509 | ||||||
| chr8:97026517
|
A | C | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-2886A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026517 | ||||||
| chr8:97026523
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.962-2880C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026523 | ||||||
| chr8:97026606
|
C | T | 1 | a0001c0002t0001g0071 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.962-2797C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026606 | ||||||
| chr8:97026964
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.962-2439G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97026964 | ||||||
| chr8:97027274
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.962-2129G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97027274 | ||||||
| chr8:97027777
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(2): Show | 5 | HG00733.hp2 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-1626A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97027777 | ||||||
| chr8:97028169
|
T | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-1234T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028169 | ||||||
| chr8:97028197
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.962-1206A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028197 | ||||||
| chr8:97028226
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-1177C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028226 | ||||||
| chr8:97028282
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-1121G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028282 | ||||||
| chr8:97028354
|
G | C | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.962-1049G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028354 | ||||||
| chr8:97028403
|
G | T | 1 | a0001c0002t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.962-1000G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028403 | ||||||
| chr8:97028599
|
G | A | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.962-804G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028599 | ||||||
| chr8:97028632
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.962-771C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97028632 | ||||||
| chr8:97029043
|
A | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0002t0001g0115others(7): Show | 10 | HG01943.hp1 HG02004.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.962-360A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 5/7 | chr8 | 97029043 | ||||||
| chr8:97029588
|
G | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+94G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97029588 | ||||||
| chr8:97029898
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+404A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97029898 | ||||||
| chr8:97030516
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1053+1022T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97030516 | ||||||
| chr8:97030697
|
C | T | 30 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.1053+1203C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97030697 | ||||||
| chr8:97030888
|
G | A | 18 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(15): Show | 18 | HG00733.hp1 HG01081.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.1053+1394G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97030888 | ||||||
| chr8:97031188
|
C | CT | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.1053+1710dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97031188 | |||||
| chr8:97031188
|
C | CTT | 4 | a0001c0002t0001g0084a0001c0002t0003g0001a0001c0004t0001g0107others(1): Show | 4 | HG02970.hp2 NA18522.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+1709_1053+171 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97031188 | |||||
| chr8:97031261
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1053+1767A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97031261 | ||||||
| chr8:97031273
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+1779G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97031273 | ||||||
| chr8:97031590
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+2096A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97031590 | ||||||
| chr8:97031653
|
G | A | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+2159G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97031653 | ||||||
| chr8:97031751
|
C | T | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1053+2257C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97031751 | ||||||
| chr8:97031949
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053+2455A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97031949 | ||||||
| chr8:97032256
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1053+2762G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97032256 | ||||||
| chr8:97032515
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+3021G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97032515 | ||||||
| chr8:97032736
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1053+3242G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97032736 | ||||||
| chr8:97032798
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+3304A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97032798 | ||||||
| chr8:97032978
|
T | G | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+3484T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97032978 | ||||||
| chr8:97033044
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1053+3550G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97033044 | ||||||
| chr8:97033103
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1053+3609G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97033103 | ||||||
| chr8:97033441
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+3947C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97033441 | ||||||
| chr8:97033562
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053+4068T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97033562 | ||||||
| chr8:97034025
|
A | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+4531A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97034025 | ||||||
| chr8:97034106
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1053+4612G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97034106 | ||||||
| chr8:97034712
|
T | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+5218T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97034712 | ||||||
| chr8:97035246
|
A | G | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+5752A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035246 | ||||||
| chr8:97035418
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+5924T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035418 | ||||||
| chr8:97035576
|
A | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(36): Show | 39 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.1053+6082A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035576 | ||||||
| chr8:97035697
|
TTTGTA | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1053+6208_1053+621 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97035697 | |||||
| chr8:97035722
|
A | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+6228A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035722 | ||||||
| chr8:97035746
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+6252C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035746 | ||||||
| chr8:97035793
|
C | T | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1053+6299C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035793 | ||||||
| chr8:97035794
|
G | A | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+6300G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97035794 | ||||||
| chr8:97036042
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+6548A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97036042 | ||||||
| chr8:97036088
|
T | C | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1053+6594T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97036088 | ||||||
| chr8:97036360
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(41): Show | 44 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(41): Show |
intron_variant | MODIFIER | c.1053+6866C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97036360 | ||||||
| chr8:97036400
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+6906G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97036400 | ||||||
| chr8:97037112
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1053+7618A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97037112 | ||||||
| chr8:97037407
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1053+7913G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97037407 | ||||||
| chr8:97037479
|
G | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+7985G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97037479 | ||||||
| chr8:97038054
|
C | T | 19 | a0001c0001t0001g0110a0001c0002t0001g0002a0001c0002t0001g0003others(16): Show | 19 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1053+8560C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97038054 | ||||||
| chr8:97038106
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1053+8612T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97038106 | ||||||
| chr8:97038127
|
G | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+8633G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97038127 | ||||||
| chr8:97038283
|
C | T | 40 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0034others(37): Show | 40 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1053+8789C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97038283 | ||||||
| chr8:97038353
|
CTTCTGGC others(9): Show |
C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+8865_1053+888 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97038353 | |||||
| chr8:97038635
|
G | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+9141G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97038635 | ||||||
| chr8:97038825
|
CA | C | 40 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(37): Show | 40 | HG00099.hp2 HG01081.hp2 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.1053+9355delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97038825 | |||||
| chr8:97038825
|
CAA | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0034others(27): Show | 30 | HG00733.hp1 HG00733.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1053+9354_1053+935 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97038825 | |||||
| chr8:97038825
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+9345_1053+935 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97038825 | |||||
| chr8:97038868
|
T | C | 1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1053+9374T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97038868 | ||||||
| chr8:97039191
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1053+9697G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039191 | ||||||
| chr8:97039196
|
T | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+9702T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039196 | ||||||
| chr8:97039206
|
G | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(41): Show | 44 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(41): Show |
intron_variant | MODIFIER | c.1053+9712G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039206 | ||||||
| chr8:97039243
|
G | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+9749G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039243 | ||||||
| chr8:97039295
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1053+9801G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039295 | ||||||
| chr8:97039306
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1053+9812T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039306 | ||||||
| chr8:97039439
|
T | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+9945T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039439 | ||||||
| chr8:97039460
|
C | CT | 4 | a0001c0001t0001g0047a0001c0001t0002g0044a0002c0003t0001g0087others(1): Show | 4 | HG01943.hp1 HG02004.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+9976dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97039460 | |||||
| chr8:97039536
|
G | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+10042G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039536 | ||||||
| chr8:97039753
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1053+10259G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039753 | ||||||
| chr8:97039880
|
C | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+10386C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039880 | ||||||
| chr8:97039923
|
A | G | 3 | a0001c0002t0001g0123a0001c0007t0001g0038a0001c0008t0001g0116 | 3 | HG02647.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1053+10429A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039923 | ||||||
| chr8:97039935
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+10441A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97039935 | ||||||
| chr8:97040047
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+10553G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040047 | ||||||
| chr8:97040053
|
G | A | 1 | a0001c0002t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1053+10559G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040053 | ||||||
| chr8:97040085
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053+10591T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040085 | ||||||
| chr8:97040195
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+10701T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040195 | ||||||
| chr8:97040233
|
C | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1053+10739C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040233 | ||||||
| chr8:97040496
|
T | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+11002T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040496 | ||||||
| chr8:97040799
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0002g0044others(4): Show | 7 | HG01943.hp1 HG02004.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1053+11305C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040799 | ||||||
| chr8:97040896
|
A | G | 29 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1053+11402A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040896 | ||||||
| chr8:97040964
|
C | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+11470C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97040964 | ||||||
| chr8:97041049
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1053+11555C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041049 | ||||||
| chr8:97041064
|
T | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+11570T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041064 | ||||||
| chr8:97041066
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0113 | 2 | NA18747.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1053+11572G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041066 | ||||||
| chr8:97041082
|
A | C | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1053+11588A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041082 | ||||||
| chr8:97041091
|
T | C | 2 | a0001c0002t0001g0073a0001c0002t0001g0113 | 2 | NA18747.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1053+11597T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041091 | ||||||
| chr8:97041122
|
G | A | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+11628G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041122 | ||||||
| chr8:97041162
|
A | T | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1053+11668A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041162 | ||||||
| chr8:97041240
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1053+11746A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041240 | ||||||
| chr8:97041356
|
G | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(8): Show | 11 | HG00733.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1053+11862G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041356 | ||||||
| chr8:97041520
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1053+12026T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041520 | ||||||
| chr8:97041693
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1053+12199G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041693 | ||||||
| chr8:97041798
|
C | T | 1 | a0001c0007t0001g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1053+12304C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041798 | ||||||
| chr8:97041799
|
G | A | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1053+12305G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041799 | ||||||
| chr8:97041805
|
T | C | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+12311T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041805 | ||||||
| chr8:97041816
|
T | G | 2 | a0001c0001t0001g0014a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1053+12322T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041816 | ||||||
| chr8:97041947
|
T | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+12453T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97041947 | ||||||
| chr8:97042008
|
T | A | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1053+12514T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042008 | ||||||
| chr8:97042023
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1053+12529T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042023 | ||||||
| chr8:97042111
|
G | C | 1 | a0001c0001t0002g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1053+12617G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042111 | ||||||
| chr8:97042160
|
A | G | 33 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0110others(30): Show | 33 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.1053+12666A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042160 | ||||||
| chr8:97042163
|
G | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+12669G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042163 | ||||||
| chr8:97042191
|
A | G | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1053+12697A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042191 | ||||||
| chr8:97042210
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+12716T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042210 | ||||||
| chr8:97042236
|
T | G | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+12742T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042236 | ||||||
| chr8:97042271
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+12777G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042271 | ||||||
| chr8:97042274
|
A | G | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+12780A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042274 | ||||||
| chr8:97042275
|
A | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+12781A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042275 | ||||||
| chr8:97042287
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+12793T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042287 | ||||||
| chr8:97042321
|
C | T | 1 | a0001c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1053+12827C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042321 | ||||||
| chr8:97042322
|
G | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1053+12828G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042322 | ||||||
| chr8:97042485
|
T | C | 1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1053+12991T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042485 | ||||||
| chr8:97042489
|
G | T | 1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1053+12995G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042489 | ||||||
| chr8:97042498
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+13004C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042498 | ||||||
| chr8:97042500
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1053+13006A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042500 | ||||||
| chr8:97042546
|
C | G | 37 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0047others(34): Show | 37 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.1053+13052C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042546 | ||||||
| chr8:97042574
|
T | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+13080T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042574 | ||||||
| chr8:97042735
|
C | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0029others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1053+13241C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042735 | ||||||
| chr8:97042778
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1053+13284C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042778 | ||||||
| chr8:97042900
|
T | G | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1053+13406T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042900 | ||||||
| chr8:97042922
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1053+13428T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042922 | ||||||
| chr8:97042927
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1053+13433C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042927 | ||||||
| chr8:97042928
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(42): Show | 45 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1053+13434G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97042928 | ||||||
| chr8:97043183
|
A | G | 1 | a0001c0002t0001g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1053+13689A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043183 | ||||||
| chr8:97043283
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1053+13789G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043283 | ||||||
| chr8:97043301
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+13807A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043301 | ||||||
| chr8:97043446
|
C | CCAGTCTG others(318): Show |
1 | a0001c0001t0001g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1053+13967_1053+13 others(331): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97043446 | |||||
| chr8:97043446
|
C | CCAGTCTG others(320): Show |
1 | a0006c0010t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1053+13967_1053+13 others(333): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97043446 | |||||
| chr8:97043511
|
C | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+14017C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043511 | ||||||
| chr8:97043513
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053+14019A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043513 | ||||||
| chr8:97043551
|
A | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+14057A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043551 | ||||||
| chr8:97043554
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+14060G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043554 | ||||||
| chr8:97043626
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(43): Show | 46 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1053+14132G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043626 | ||||||
| chr8:97043773
|
T | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+14279T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043773 | ||||||
| chr8:97043787
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+14293C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97043787 | ||||||
| chr8:97044535
|
C | G | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+15041C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044535 | ||||||
| chr8:97044549
|
C | G | 1 | a0001c0002t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1053+15055C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044549 | ||||||
| chr8:97044560
|
T | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+15066T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044560 | ||||||
| chr8:97044753
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+15259C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044753 | ||||||
| chr8:97044754
|
G | A | 1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1053+15260G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044754 | ||||||
| chr8:97044789
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+15295C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044789 | ||||||
| chr8:97044814
|
C | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+15320C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044814 | ||||||
| chr8:97044897
|
G | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+15403G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044897 | ||||||
| chr8:97044920
|
G | T | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1053+15426G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044920 | ||||||
| chr8:97044933
|
G | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+15439G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044933 | ||||||
| chr8:97044986
|
C | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0029others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1053+15492C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97044986 | ||||||
| chr8:97045214
|
G | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0124 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1053+15720G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045214 | ||||||
| chr8:97045253
|
C | CAA | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+15760_1053+15 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97045253 | |||||
| chr8:97045297
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1053+15803C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045297 | ||||||
| chr8:97045297
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1053+15803C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045297 | ||||||
| chr8:97045304
|
T | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1053+15810T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045304 | ||||||
| chr8:97045344
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+15850C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045344 | ||||||
| chr8:97045349
|
C | T | 5 | a0001c0001t0001g0047a0001c0002t0001g0084a0001c0004t0001g0107others(2): Show | 5 | HG01943.hp1 HG02004.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+15855C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045349 | ||||||
| chr8:97045368
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1053+15874C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045368 | ||||||
| chr8:97045440
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1053+15946C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045440 | ||||||
| chr8:97045478
|
C | T | 4 | a0001c0001t0001g0028a0003c0005t0001g0007a0003c0005t0001g0068others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+15984C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045478 | ||||||
| chr8:97045502
|
C | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0055a0001c0002t0002g0050others(1): Show | 4 | HG01261.hp1 HG01978.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+16008C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045502 | ||||||
| chr8:97045525
|
G | A | 1 | a0002c0003t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1053+16031G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045525 | ||||||
| chr8:97045577
|
C | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0002t0001g0025others(6): Show | 9 | HG01261.hp1 HG01517.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1053+16083C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045577 | ||||||
| chr8:97045890
|
C | G | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+16396C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045890 | ||||||
| chr8:97045891
|
G | A | 2 | a0001c0002t0001g0115a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1053+16397G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045891 | ||||||
| chr8:97045920
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1053+16426G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045920 | ||||||
| chr8:97045946
|
A | G | 29 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0029others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1053+16452A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97045946 | ||||||
| chr8:97046254
|
G | A | 1 | a0003c0005t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1053+16760G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046254 | ||||||
| chr8:97046401
|
G | T | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053+16907G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046401 | ||||||
| chr8:97046484
|
C | G | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053+16990C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046484 | ||||||
| chr8:97046577
|
G | A | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1053+17083G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046577 | ||||||
| chr8:97046818
|
A | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(42): Show | 45 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(42): Show |
intron_variant | MODIFIER | c.1053+17324A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046818 | ||||||
| chr8:97046943
|
C | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(43): Show | 46 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1053+17449C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046943 | ||||||
| chr8:97046986
|
TG | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1053+17493delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046986 | ||||||
| chr8:97046987
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+17493G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97046987 | ||||||
| chr8:97047133
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1053+17639C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047133 | ||||||
| chr8:97047175
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(32): Show | 35 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.1053+17681T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047175 | ||||||
| chr8:97047501
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+18007C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047501 | ||||||
| chr8:97047606
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1053+18112G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047606 | ||||||
| chr8:97047686
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1053+18192T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047686 | ||||||
| chr8:97047721
|
T | C | 50 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1053+18227T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047721 | ||||||
| chr8:97047754
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054-18255G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047754 | ||||||
| chr8:97047808
|
A | G | 4 | a0001c0001t0002g0021a0001c0002t0001g0121a0001c0002t0002g0085others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-18201A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047808 | ||||||
| chr8:97047831
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054-18178T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047831 | ||||||
| chr8:97047906
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1054-18103A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97047906 | ||||||
| chr8:97048228
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1054-17781G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97048228 | ||||||
| chr8:97048233
|
G | A | 18 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(15): Show | 18 | HG00733.hp1 HG01081.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054-17776G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97048233 | ||||||
| chr8:97048267
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-17742T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97048267 | ||||||
| chr8:97048712
|
G | C | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-17297G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97048712 | ||||||
| chr8:97048948
|
G | A | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1054-17061G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97048948 | ||||||
| chr8:97049116
|
G | A | 28 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0029others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.1054-16893G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97049116 | ||||||
| chr8:97049118
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1054-16891G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97049118 | ||||||
| chr8:97049136
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1054-16873C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97049136 | ||||||
| chr8:97049211
|
T | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-16798T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97049211 | ||||||
| chr8:97049521
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1054-16488C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97049521 | ||||||
| chr8:97049931
|
C | G | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1054-16078C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97049931 | ||||||
| chr8:97050608
|
T | C | 31 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.1054-15401T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97050608 | ||||||
| chr8:97050646
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1054-15363C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97050646 | ||||||
| chr8:97050679
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(43): Show | 46 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1054-15330C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97050679 | ||||||
| chr8:97051343
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-14666A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97051343 | ||||||
| chr8:97051505
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1054-14504A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97051505 | ||||||
| chr8:97052012
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-13997A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97052012 | ||||||
| chr8:97052028
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-13981C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97052028 | ||||||
| chr8:97052196
|
A | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-13813A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97052196 | ||||||
| chr8:97052210
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1054-13799A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97052210 | ||||||
| chr8:97053487
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077 | 3 | NA18945.hp2 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1054-12522G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97053487 | ||||||
| chr8:97053674
|
G | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1054-12335G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97053674 | ||||||
| chr8:97053690
|
G | C | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1054-12319G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97053690 | ||||||
| chr8:97053951
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(45): Show | 48 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.1054-12058C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97053951 | ||||||
| chr8:97053960
|
A | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(38): Show | 41 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(38): Show |
intron_variant | MODIFIER | c.1054-12049A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97053960 | ||||||
| chr8:97054032
|
T | C | 2 | a0001c0001t0002g0021a0001c0002t0001g0121 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1054-11977T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054032 | ||||||
| chr8:97054043
|
C | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(38): Show | 41 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(38): Show |
intron_variant | MODIFIER | c.1054-11966C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054043 | ||||||
| chr8:97054071
|
T | C | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1054-11938T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054071 | ||||||
| chr8:97054133
|
A | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-11876A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054133 | ||||||
| chr8:97054222
|
G | C | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1054-11787G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054222 | ||||||
| chr8:97054289
|
A | G | 2 | a0001c0002t0001g0120a0002c0003t0001g0053 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1054-11720A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054289 | ||||||
| chr8:97054450
|
T | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(35): Show | 38 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.1054-11559T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054450 | ||||||
| chr8:97054575
|
G | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(35): Show | 38 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.1054-11434G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054575 | ||||||
| chr8:97054617
|
CA | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(17): Show | 20 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.1054-11391delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054617 | ||||||
| chr8:97054740
|
G | A | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-11269G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97054740 | ||||||
| chr8:97055049
|
TC | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(39): Show | 42 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(39): Show |
intron_variant | MODIFIER | c.1054-10955delC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97055049 | |||||
| chr8:97055215
|
T | C | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1054-10794T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055215 | ||||||
| chr8:97055553
|
C | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-10456C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055553 | ||||||
| chr8:97055582
|
C | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(39): Show | 42 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(39): Show |
intron_variant | MODIFIER | c.1054-10427C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055582 | ||||||
| chr8:97055588
|
G | C | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1054-10421G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055588 | ||||||
| chr8:97055638
|
G | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-10371G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055638 | ||||||
| chr8:97055882
|
C | T | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1054-10127C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055882 | ||||||
| chr8:97055912
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1054-10097C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055912 | ||||||
| chr8:97055920
|
C | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(32): Show | 35 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.1054-10089C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055920 | ||||||
| chr8:97055959
|
G | A | 10 | a0001c0001t0002g0021a0001c0002t0001g0005a0001c0002t0001g0006others(7): Show | 10 | HG01261.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1054-10050G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97055959 | ||||||
| chr8:97056101
|
A | AAC | 7 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(4): Show | 7 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054-9878_1054-987 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97056101 | |||||
| chr8:97056101
|
A | AACAC | 2 | a0001c0001t0001g0016a0001c0001t0001g0019 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1054-9880_1054-987 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97056101 | |||||
| chr8:97056101
|
AAC | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(33): Show | 36 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.1054-9878_1054-987 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97056101 | |||||
| chr8:97056101
|
AACAC | A | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1054-9880_1054-987 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97056101 | |||||
| chr8:97056109
|
C | T | 2 | a0001c0002t0001g0084a0001c0002t0001g0120 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1054-9900C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97056109 | ||||||
| chr8:97056111
|
C | T | 36 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(33): Show | 36 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.1054-9898C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97056111 | ||||||
| chr8:97056410
|
A | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0002g0029others(26): Show | 29 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.1054-9599A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97056410 | ||||||
| chr8:97056759
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1054-9250T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97056759 | ||||||
| chr8:97056813
|
C | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-9196C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97056813 | ||||||
| chr8:97057161
|
G | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(34): Show | 37 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.1054-8848G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057161 | ||||||
| chr8:97057185
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1054-8824C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057185 | ||||||
| chr8:97057202
|
C | T | 1 | a0001c0002t0003g0001 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1054-8807C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057202 | ||||||
| chr8:97057317
|
G | A | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-8692G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057317 | ||||||
| chr8:97057331
|
T | A | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1054-8678T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057331 | ||||||
| chr8:97057386
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-8623G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057386 | ||||||
| chr8:97057513
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1054-8496A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057513 | ||||||
| chr8:97057527
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-8482T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057527 | ||||||
| chr8:97057863
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1054-8146C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97057863 | ||||||
| chr8:97058136
|
T | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-7873T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97058136 | ||||||
| chr8:97058189
|
A | G | 1 | a0001c0004t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1054-7820A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97058189 | ||||||
| chr8:97058278
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1054-7731T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97058278 | ||||||
| chr8:97058317
|
C | T | 2 | a0001c0002t0001g0084a0001c0002t0001g0093 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1054-7692C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97058317 | ||||||
| chr8:97059242
|
G | A | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1054-6767G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97059242 | ||||||
| chr8:97059318
|
A | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-6691A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97059318 | ||||||
| chr8:97059321
|
T | A | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-6688T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97059321 | ||||||
| chr8:97059579
|
C | G | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1054-6430C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97059579 | ||||||
| chr8:97059848
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1054-6161G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97059848 | ||||||
| chr8:97060047
|
TG | T | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1054-5960delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97060047 | |||||
| chr8:97060370
|
T | C | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-5639T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97060370 | ||||||
| chr8:97060505
|
T | C | 2 | a0001c0001t0001g0014a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1054-5504T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97060505 | ||||||
| chr8:97060526
|
A | T | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1054-5483A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97060526 | ||||||
| chr8:97060800
|
CTGAG | C | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1054-5206_1054-520 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97060800 | |||||
| chr8:97060870
|
C | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(5): Show | 8 | HG02273.hp2 HG03017.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054-5139C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97060870 | ||||||
| chr8:97061008
|
A | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1054-5001A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061008 | ||||||
| chr8:97061094
|
A | T | 3 | a0001c0001t0001g0010a0001c0002t0001g0115a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1054-4915A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061094 | ||||||
| chr8:97061268
|
TGTTTTC | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-4740_1054-473 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061268 | ||||||
| chr8:97061358
|
AAAAAGTT others(19): Show |
A | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1054-4650_1054-462 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061358 | ||||||
| chr8:97061575
|
T | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-4434T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061575 | ||||||
| chr8:97061923
|
G | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054-4086G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061923 | ||||||
| chr8:97061996
|
C | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-4013C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97061996 | ||||||
| chr8:97062143
|
CACTT | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0002t0001g0002others(23): Show | 26 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1054-3864_1054-386 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97062143 | |||||
| chr8:97062151
|
G | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-3858G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97062151 | ||||||
| chr8:97062356
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-3653C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97062356 | ||||||
| chr8:97062629
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-3380A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97062629 | ||||||
| chr8:97062887
|
A | C | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1054-3122A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97062887 | ||||||
| chr8:97062938
|
C | T | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-3071C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97062938 | ||||||
| chr8:97063052
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-2957G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063052 | ||||||
| chr8:97063268
|
C | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(36): Show | 39 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.1054-2741C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063268 | ||||||
| chr8:97063322
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1054-2687G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063322 | ||||||
| chr8:97063332
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-2677T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063332 | ||||||
| chr8:97063385
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054-2624C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063385 | ||||||
| chr8:97063414
|
T | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(40): Show | 43 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(40): Show |
intron_variant | MODIFIER | c.1054-2595T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063414 | ||||||
| chr8:97063537
|
A | T | 43 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(40): Show | 43 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(40): Show |
intron_variant | MODIFIER | c.1054-2472A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063537 | ||||||
| chr8:97063558
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-2451A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063558 | ||||||
| chr8:97063656
|
A | G | 31 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.1054-2353A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063656 | ||||||
| chr8:97063864
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1054-2145C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063864 | ||||||
| chr8:97063865
|
G | A | 18 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(15): Show | 18 | HG00733.hp1 HG01081.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054-2144G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063865 | ||||||
| chr8:97063897
|
C | T | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-2112C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063897 | ||||||
| chr8:97063903
|
G | T | 1 | a0001c0001t0001g0031 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1054-2106G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97063903 | ||||||
| chr8:97064056
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0108 | 3 | HG02040.hp2 NA19005.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1054-1953G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064056 | ||||||
| chr8:97064117
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1054-1892G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064117 | ||||||
| chr8:97064206
|
A | G | 52 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1054-1803A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064206 | ||||||
| chr8:97064372
|
T | C | 4 | a0001c0001t0001g0047a0001c0004t0001g0107a0001c0004t0001g0114others(1): Show | 4 | HG01943.hp1 HG02004.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054-1637T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064372 | ||||||
| chr8:97064457
|
A | C | 2 | a0001c0001t0001g0014a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1054-1552A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064457 | ||||||
| chr8:97064636
|
C | T | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1054-1373C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064636 | ||||||
| chr8:97064707
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-1302G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064707 | ||||||
| chr8:97064752
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1054-1257T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064752 | ||||||
| chr8:97064844
|
T | C | 1 | a0001c0002t0001g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1054-1165T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064844 | ||||||
| chr8:97064888
|
T | A | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1054-1121T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064888 | ||||||
| chr8:97064917
|
G | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1054-1092G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97064917 | ||||||
| chr8:97065032
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-977T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97065032 | ||||||
| chr8:97065211
|
T | TA | 38 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(35): Show | 38 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.1054-795dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 97065211 | |||||
| chr8:97065836
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054-173G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 6/7 | chr8 | 97065836 | ||||||
| chr8:97066359
|
T | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+149T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066359 | ||||||
| chr8:97066865
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+655G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066865 | ||||||
| chr8:97066866
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1255+656G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066866 | ||||||
| chr8:97066873
|
G | A | 3 | a0001c0001t0001g0014a0001c0002t0001g0123a0001c0002t0002g0004 | 3 | HG02257.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1255+663G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066873 | ||||||
| chr8:97066910
|
AAC | A | 4 | a0001c0002t0001g0092a0001c0002t0001g0094a0001c0002t0001g0120others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+702_1255+703d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066910 | |||||
| chr8:97066913
|
A | T | 1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1255+703A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066913 | ||||||
| chr8:97066914
|
G | T | 1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1255+704G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066914 | ||||||
| chr8:97066916
|
C | CT | 30 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0046others(27): Show | 30 | HG01081.hp2 HG01943.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1255+735dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066916 | |||||
| chr8:97066916
|
C | CTT | 6 | a0001c0001t0001g0014a0001c0002t0001g0002a0001c0002t0001g0003others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+734_1255+735d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066916 | |||||
| chr8:97066916
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1255+706C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97066916 | ||||||
| chr8:97066916
|
CTT | C | 9 | a0001c0001t0001g0070a0001c0001t0001g0108a0001c0001t0001g0117others(6): Show | 9 | HG02040.hp2 HG02922.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255+734_1255+735d others(4): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066916 | |||||
| chr8:97066916
|
CTTT | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(37): Show | 40 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1255+733_1255+735d others(5): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066916 | |||||
| chr8:97066916
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1255+724_1255+735d others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066916 | |||||
| chr8:97066916
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255+720_1255+735d others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97066916 | |||||
| chr8:97067047
|
C | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+837C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97067047 | ||||||
| chr8:97067109
|
C | T | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(54): Show | 57 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1255+899C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97067109 | ||||||
| chr8:97067261
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+1051A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97067261 | ||||||
| chr8:97067407
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+1197C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97067407 | ||||||
| chr8:97067909
|
T | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1255+1699T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97067909 | ||||||
| chr8:97067997
|
A | C | 18 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0048others(15): Show | 18 | HG00733.hp1 HG01081.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.1255+1787A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97067997 | ||||||
| chr8:97068188
|
G | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0013 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1255+1978G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97068188 | ||||||
| chr8:97068740
|
A | G | 50 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(47): Show | 50 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1255+2530A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97068740 | ||||||
| chr8:97068770
|
G | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.1255+2560G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97068770 | ||||||
| chr8:97068863
|
C | G | 50 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(47): Show | 50 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1255+2653C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97068863 | ||||||
| chr8:97069186
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.1255+2976G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069186 | ||||||
| chr8:97069235
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1255+3025T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069235 | ||||||
| chr8:97069342
|
T | A | 5 | a0001c0001t0001g0047a0001c0002t0001g0084a0001c0004t0001g0107others(2): Show | 5 | HG01943.hp1 HG02004.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+3132T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069342 | ||||||
| chr8:97069433
|
T | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+3223T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069433 | ||||||
| chr8:97069459
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+3249C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069459 | ||||||
| chr8:97069471
|
A | C | 30 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.1255+3261A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069471 | ||||||
| chr8:97069475
|
A | G | 3 | a0001c0001t0001g0014a0001c0002t0001g0123a0001c0002t0002g0004 | 3 | HG02257.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1255+3265A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069475 | ||||||
| chr8:97069726
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+3516C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069726 | ||||||
| chr8:97069752
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1255+3542G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97069752 | ||||||
| chr8:97070186
|
C | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0125others(7): Show | 10 | HG02004.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1255+3976C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97070186 | ||||||
| chr8:97070500
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1255+4290T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97070500 | ||||||
| chr8:97070594
|
T | C | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1255+4384T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97070594 | ||||||
| chr8:97071088
|
A | G | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1255+4878A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97071088 | ||||||
| chr8:97071504
|
A | C | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1255+5294A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97071504 | ||||||
| chr8:97071528
|
C | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0114 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1255+5318C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97071528 | ||||||
| chr8:97071854
|
C | T | 50 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(47): Show | 50 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1255+5644C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97071854 | ||||||
| chr8:97071878
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1255+5668G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97071878 | ||||||
| chr8:97071932
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1255+5722G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97071932 | ||||||
| chr8:97072163
|
T | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+5953T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97072163 | ||||||
| chr8:97072489
|
G | A | 2 | a0001c0001t0001g0028a0008c0011t0002g0037 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1255+6279G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97072489 | ||||||
| chr8:97072961
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0112 | 2 | HG02273.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1255+6751T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97072961 | ||||||
| chr8:97073037
|
A | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1255+6827A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073037 | ||||||
| chr8:97073143
|
C | A | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1255+6933C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073143 | ||||||
| chr8:97073229
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+7019T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073229 | ||||||
| chr8:97073234
|
A | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1255+7024A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073234 | ||||||
| chr8:97073307
|
C | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+7097C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073307 | ||||||
| chr8:97073473
|
A | G | 3 | a0001c0001t0001g0028a0001c0002t0001g0084a0008c0011t0002g0037 | 3 | HG02970.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1255+7263A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073473 | ||||||
| chr8:97073565
|
T | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1255+7355T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073565 | ||||||
| chr8:97073620
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1255+7410G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97073620 | ||||||
| chr8:97074520
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1255+8310C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074520 | ||||||
| chr8:97074635
|
G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077others(2): Show | 5 | NA18747.hp2 NA18945.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255+8425G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074635 | ||||||
| chr8:97074664
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0002g0029others(1): Show | 4 | HG01517.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+8454G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074664 | ||||||
| chr8:97074685
|
C | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(44): Show | 47 | HG00733.hp1 HG00733.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1255+8475C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074685 | ||||||
| chr8:97074696
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1255+8486G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074696 | ||||||
| chr8:97074974
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1255+8764T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074974 | ||||||
| chr8:97074984
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0002g0029others(1): Show | 4 | HG01517.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+8774G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97074984 | ||||||
| chr8:97075071
|
C | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+8861C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97075071 | ||||||
| chr8:97075110
|
C | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(30): Show | 33 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.1255+8900C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97075110 | ||||||
| chr8:97075486
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1255+9276G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97075486 | ||||||
| chr8:97075611
|
GA | G | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(57): Show | 60 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1255+9405delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97075611 | |||||
| chr8:97076576
|
T | C | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1255+10366T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97076576 | ||||||
| chr8:97077569
|
T | G | 1 | a0001c0001t0002g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1255+11359T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97077569 | ||||||
| chr8:97077834
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0002g0029others(1): Show | 4 | HG01517.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+11624A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97077834 | ||||||
| chr8:97077909
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1255+11699C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97077909 | ||||||
| chr8:97078354
|
G | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1255+12144G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97078354 | ||||||
| chr8:97078358
|
G | A | 48 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(45): Show | 48 | HG00733.hp1 HG00733.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1255+12148G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97078358 | ||||||
| chr8:97078763
|
T | TTC | 9 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0002t0001g0006others(6): Show | 9 | HG00733.hp1 HG01261.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255+12596_1255+12 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
T | TTCTC | 9 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0078others(6): Show | 9 | HG01081.hp1 HG01255.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255+12594_1255+12 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
T | TTCTCTC | 8 | a0001c0001t0001g0070a0001c0001t0001g0102a0001c0001t0001g0108others(5): Show | 8 | HG01981.hp1 HG02040.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255+12592_1255+12 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
T | TTCTCTCT others(1): Show |
3 | a0001c0001t0001g0056a0001c0001t0001g0109a0001c0002t0001g0113 | 3 | HG01978.hp2 NA18962.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1255+12590_1255+12 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
T | TTCTCTCT others(5): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0057 | 2 | HG03927.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1255+12586_1255+12 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTC | T | 22 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0036others(19): Show | 22 | HG01975.hp1 HG01978.hp1 HG02273.hp2 others(19): Show |
intron_variant | MODIFIER | c.1255+12596_1255+12 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTCTC | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0027others(8): Show | 11 | HG00733.hp2 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1255+12594_1255+12 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTCTCTC | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(24): Show | 27 | HG01081.hp2 HG02004.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.1255+12592_1255+12 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTCTCTCT others(1): Show |
T | 5 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0079others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255+12590_1255+12 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTCTCTCT others(3): Show |
T | 5 | a0001c0001t0001g0047a0001c0002t0001g0088a0003c0005t0001g0007others(2): Show | 5 | HG01943.hp1 HG02004.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255+12588_1255+12 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTCTCTCT others(5): Show |
T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+12586_1255+12 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078763
|
TTCTCTCT others(9): Show |
T | 8 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1255+12582_1255+12 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97078763 | |||||
| chr8:97078807
|
C | CTCT | 3 | a0001c0001t0002g0021a0001c0002t0001g0121a0001c0002t0001g0122 | 3 | HG02055.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1255+12597_1255+12 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97078807 | ||||||
| chr8:97078952
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1255+12742T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97078952 | ||||||
| chr8:97079049
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+12839C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079049 | ||||||
| chr8:97079143
|
T | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+12933T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079143 | ||||||
| chr8:97079345
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1255+13135G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079345 | ||||||
| chr8:97079450
|
A | C | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1255+13240A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079450 | ||||||
| chr8:97079836
|
G | T | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1255+13626G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079836 | ||||||
| chr8:97079963
|
A | C | 1 | a0001c0002t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1255+13753A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079963 | ||||||
| chr8:97079969
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1255+13759T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97079969 | ||||||
| chr8:97080309
|
G | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1255+14099G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080309 | ||||||
| chr8:97080341
|
GACATTTC others(12): Show |
G | 51 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(48): Show | 51 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255+14140_1255+14 others(25): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97080341 | |||||
| chr8:97080360
|
A | G | 46 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(43): Show | 46 | HG00099.hp2 HG01081.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.1255+14150A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080360 | ||||||
| chr8:97080484
|
A | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(32): Show | 35 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.1255+14274A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080484 | ||||||
| chr8:97080501
|
T | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(48): Show | 51 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255+14291T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080501 | ||||||
| chr8:97080608
|
G | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0079others(3): Show | 6 | HG00099.hp2 HG03195.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+14398G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080608 | ||||||
| chr8:97080698
|
G | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0110others(25): Show | 28 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.1255+14488G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080698 | ||||||
| chr8:97080802
|
C | T | 1 | a0001c0002t0001g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1255+14592C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080802 | ||||||
| chr8:97080823
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1255+14613G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080823 | ||||||
| chr8:97080902
|
A | G | 2 | a0001c0001t0001g0026a0001c0002t0001g0111 | 2 | HG00099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1255+14692A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97080902 | ||||||
| chr8:97080907
|
C | CCCTTCTT others(13): Show |
51 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(48): Show | 51 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255+14724_1255+14 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97080907 | |||||
| chr8:97081041
|
A | G | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1255+14831A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081041 | ||||||
| chr8:97081098
|
AT | A | 2 | a0001c0001t0001g0061a0001c0002t0001g0059 | 2 | HG01975.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1255+14889delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081098 | ||||||
| chr8:97081214
|
C | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(27): Show |
intron_variant | MODIFIER | c.1255+15004C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081214 | ||||||
| chr8:97081613
|
A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+15403A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081613 | ||||||
| chr8:97081707
|
A | T | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1255+15497A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081707 | ||||||
| chr8:97081807
|
G | A | 1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255+15597G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081807 | ||||||
| chr8:97081972
|
G | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+15762G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97081972 | ||||||
| chr8:97082090
|
A | G | 52 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(49): Show | 52 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1255+15880A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97082090 | ||||||
| chr8:97082352
|
T | C | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1255+16142T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97082352 | ||||||
| chr8:97082383
|
C | CA | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0079others(3): Show | 6 | HG00099.hp2 HG03195.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+16174dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97082383 | |||||
| chr8:97082401
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+16191C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97082401 | ||||||
| chr8:97082694
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+16484C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97082694 | ||||||
| chr8:97082807
|
T | C | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255+16597T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97082807 | ||||||
| chr8:97083763
|
C | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(49): Show | 52 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1255+17553C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97083763 | ||||||
| chr8:97083875
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255+17665A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97083875 | ||||||
| chr8:97084341
|
T | C | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255+18131T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084341 | ||||||
| chr8:97084627
|
A | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255+18417A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084627 | ||||||
| chr8:97084663
|
T | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1255+18453T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084663 | ||||||
| chr8:97084675
|
G | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(27): Show | 30 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(27): Show |
intron_variant | MODIFIER | c.1255+18465G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084675 | ||||||
| chr8:97084690
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255+18480G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084690 | ||||||
| chr8:97084803
|
G | A | 1 | a0003c0005t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1255+18593G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084803 | ||||||
| chr8:97084812
|
C | CTG | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0109others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+18626_1255+18 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084812 | |||||
| chr8:97084812
|
C | CTGTG | 15 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0002g0021others(12): Show | 15 | HG01261.hp2 HG01517.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255+18624_1255+18 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084812 | |||||
| chr8:97084812
|
C | CTGTGTG | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+18622_1255+18 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084812 | |||||
| chr8:97084812
|
C | CTGTGTGT others(3): Show |
23 | a0001c0001t0001g0017a0001c0002t0001g0002a0001c0002t0001g0003others(20): Show | 23 | HG01081.hp2 HG01516.hp1 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.1255+18618_1255+18 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084812 | |||||
| chr8:97084812
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0110a0001c0002t0001g0049 | 2 | HG03927.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1255+18616_1255+18 others(18): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084812 | |||||
| chr8:97084812
|
C | CTGTGTGT others(7): Show |
1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1255+18614_1255+18 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084812 | |||||
| chr8:97084836
|
GTC | G | 3 | a0001c0001t0001g0080a0001c0004t0001g0107a0001c0004t0001g0114 | 3 | NA18522.hp2 NA19012.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1255+18632_1255+18 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97084836 | |||||
| chr8:97084838
|
C | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(48): Show | 51 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255+18628C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97084838 | ||||||
| chr8:97085305
|
T | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(30): Show | 33 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.1255+19095T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97085305 | ||||||
| chr8:97085396
|
A | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(30): Show | 33 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.1255+19186A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97085396 | ||||||
| chr8:97085397
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1255+19187C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97085397 | ||||||
| chr8:97085770
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1255+19560C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97085770 | ||||||
| chr8:97085897
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1255+19687C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97085897 | ||||||
| chr8:97085983
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1255+19773G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97085983 | ||||||
| chr8:97086289
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+20079G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97086289 | ||||||
| chr8:97086405
|
C | T | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1255+20195C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97086405 | ||||||
| chr8:97087188
|
A | C | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1255+20978A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97087188 | ||||||
| chr8:97087206
|
C | A | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1255+20996C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97087206 | ||||||
| chr8:97087290
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1255+21080G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97087290 | ||||||
| chr8:97087405
|
T | TG | 34 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(31): Show | 34 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(31): Show |
intron_variant | MODIFIER | c.1255+21201dupG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97087405 | |||||
| chr8:97087510
|
TA | T | 34 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(31): Show | 34 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(31): Show |
intron_variant | MODIFIER | c.1255+21302delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97087510 | |||||
| chr8:97087516
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1255+21306T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97087516 | ||||||
| chr8:97087699
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1255+21489A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97087699 | ||||||
| chr8:97088453
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1255+22243T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97088453 | ||||||
| chr8:97088602
|
AATTGAT | A | 2 | a0001c0001t0001g0026a0001c0002t0001g0111 | 2 | HG00099.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1255+22396_1255+22 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97088602 | |||||
| chr8:97088606
|
G | T | 1 | a0002c0003t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1255+22396G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97088606 | ||||||
| chr8:97089015
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1255+22805G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97089015 | ||||||
| chr8:97089243
|
C | CA | 75 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0023others(72): Show | 75 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.1255+23049dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97089243 | |||||
| chr8:97089243
|
C | CAA | 12 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0027others(9): Show | 12 | HG01517.hp1 HG01975.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1255+23048_1255+23 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97089243 | |||||
| chr8:97089258
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+23048A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97089258 | ||||||
| chr8:97089277
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+23067G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97089277 | ||||||
| chr8:97089405
|
A | G | 31 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1255+23195A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97089405 | ||||||
| chr8:97089732
|
A | C | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1255+23522A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97089732 | ||||||
| chr8:97090139
|
T | G | 3 | a0001c0001t0001g0010a0001c0002t0001g0115a0001c0002t0002g0039 | 3 | HG02109.hp2 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1255+23929T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97090139 | ||||||
| chr8:97090611
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1255+24401A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97090611 | ||||||
| chr8:97091037
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+24827G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091037 | ||||||
| chr8:97091098
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1255+24888G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091098 | ||||||
| chr8:97091168
|
C | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(30): Show | 33 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.1255+24958C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091168 | ||||||
| chr8:97091169
|
C | T | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1255+24959C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091169 | ||||||
| chr8:97091370
|
A | G | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0079others(3): Show | 6 | HG00099.hp2 HG03195.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+25160A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091370 | ||||||
| chr8:97091486
|
C | G | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1255+25276C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091486 | ||||||
| chr8:97091528
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+25318T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091528 | ||||||
| chr8:97091538
|
G | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0002g0029others(1): Show | 4 | HG01517.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+25328G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091538 | ||||||
| chr8:97091554
|
A | C | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1255+25344A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091554 | ||||||
| chr8:97091673
|
A | G | 2 | a0001c0001t0001g0014a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1255+25463A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091673 | ||||||
| chr8:97091854
|
A | AGATG | 17 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 17 | HG00733.hp1 HG01081.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1255+25670_1255+25 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97091854 | |||||
| chr8:97091863
|
G | A | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1255+25653G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97091863 | ||||||
| chr8:97091884
|
C | CAG | 2 | a0001c0002t0001g0025a0001c0002t0002g0050 | 2 | HG01261.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1255+25691_1255+25 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97091884 | |||||
| chr8:97092404
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1255+26194A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97092404 | ||||||
| chr8:97092405
|
A | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(33): Show | 36 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255+26195A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97092405 | ||||||
| chr8:97092861
|
G | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+26651G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97092861 | ||||||
| chr8:97093529
|
T | C | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.1255+27319T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97093529 | ||||||
| chr8:97093645
|
T | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+27435T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97093645 | ||||||
| chr8:97093865
|
T | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(33): Show | 36 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255+27655T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97093865 | ||||||
| chr8:97093869
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1255+27659C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97093869 | ||||||
| chr8:97093903
|
A | G | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1255+27693A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97093903 | ||||||
| chr8:97093935
|
A | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+27725A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97093935 | ||||||
| chr8:97094083
|
T | TC | 39 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(36): Show | 39 | HG00099.hp1 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1255+27874dupC | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97094083 | |||||
| chr8:97094086
|
CT | C | 2 | a0001c0001t0002g0044a0002c0003t0001g0087 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1255+27879delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97094086 | |||||
| chr8:97094217
|
A | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(33): Show | 36 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255+28007A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97094217 | ||||||
| chr8:97094435
|
C | A | 1 | a0001c0002t0001g0049 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1255+28225C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97094435 | ||||||
| chr8:97094440
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1255+28230G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97094440 | ||||||
| chr8:97094615
|
A | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0079others(3): Show | 6 | HG00099.hp2 HG03195.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+28405A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97094615 | ||||||
| chr8:97094756
|
A | AAT | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0079others(3): Show | 6 | HG00099.hp2 HG03195.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+28560_1255+28 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97094756 | |||||
| chr8:97095061
|
C | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(48): Show | 51 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255+28851C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095061 | ||||||
| chr8:97095222
|
G | A | 34 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0047others(31): Show | 34 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(31): Show |
intron_variant | MODIFIER | c.1255+29012G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095222 | ||||||
| chr8:97095377
|
T | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+29167T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095377 | ||||||
| chr8:97095485
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255+29275C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095485 | ||||||
| chr8:97095487
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+29277T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095487 | ||||||
| chr8:97095526
|
T | C | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1255+29316T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095526 | ||||||
| chr8:97095809
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1255+29599T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095809 | ||||||
| chr8:97095835
|
TG | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+29626delG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095835 | ||||||
| chr8:97095891
|
C | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+29681C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97095891 | ||||||
| chr8:97096054
|
G | GGAT | 23 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(20): Show | 23 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1255+29869_1255+29 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97096054 | |||||
| chr8:97096295
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255+30085A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096295 | ||||||
| chr8:97096514
|
A | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+30304A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096514 | ||||||
| chr8:97096778
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1255+30568T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096778 | ||||||
| chr8:97096795
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1255+30585G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096795 | ||||||
| chr8:97096842
|
A | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1255+30632A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096842 | ||||||
| chr8:97096923
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1255+30713G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096923 | ||||||
| chr8:97096943
|
T | C | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+30733T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97096943 | ||||||
| chr8:97097045
|
T | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(33): Show | 36 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255+30835T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97097045 | ||||||
| chr8:97097805
|
G | GGA | 34 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(31): Show | 34 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(31): Show |
intron_variant | MODIFIER | c.1255+31612_1255+31 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97097805 | |||||
| chr8:97097822
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1255+31612G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97097822 | ||||||
| chr8:97097873
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1255+31663T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97097873 | ||||||
| chr8:97098235
|
T | G | 52 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(49): Show | 52 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1255+32025T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97098235 | ||||||
| chr8:97099115
|
C | CT | 31 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(28): Show | 31 | HG00099.hp2 HG00733.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255+32932dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099115 | |||||
| chr8:97099115
|
C | CTCTCTCT others(10): Show |
2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+32906_1255+32 others(23): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099115 | |||||
| chr8:97099115
|
C | CTT | 17 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0056others(14): Show | 17 | HG00733.hp1 HG01081.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1255+32931_1255+32 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099115 | |||||
| chr8:97099115
|
C | CTTT | 34 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0048others(31): Show | 34 | HG00099.hp1 HG01081.hp2 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.1255+32930_1255+32 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099115 | |||||
| chr8:97099115
|
C | CTTTT | 5 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0084others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+32929_1255+32 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099115 | |||||
| chr8:97099115
|
CT | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077others(7): Show | 10 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1255+32932delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099115 | |||||
| chr8:97099299
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+33089T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099299 | ||||||
| chr8:97099354
|
C | T | 1 | a0001c0002t0001g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1255+33144C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099354 | ||||||
| chr8:97099369
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+33159G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099369 | ||||||
| chr8:97099416
|
C | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1255+33206C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099416 | ||||||
| chr8:97099489
|
T | C | 1 | a0001c0002t0002g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1255+33279T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099489 | ||||||
| chr8:97099550
|
GT | G | 25 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0047others(22): Show | 25 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.1255+33352delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97099550 | |||||
| chr8:97099720
|
G | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+33510G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099720 | ||||||
| chr8:97099784
|
G | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(46): Show | 49 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1255+33574G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099784 | ||||||
| chr8:97099854
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0002g0044a0001c0002t0001g0115others(2): Show | 5 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255+33644C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97099854 | ||||||
| chr8:97100184
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1255+33974G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97100184 | ||||||
| chr8:97100403
|
A | G | 31 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1255+34193A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97100403 | ||||||
| chr8:97100440
|
T | C | 2 | a0001c0001t0001g0014a0001c0002t0002g0004 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1255+34230T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97100440 | ||||||
| chr8:97100805
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+34595C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97100805 | ||||||
| chr8:97100856
|
T | C | 49 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(46): Show | 49 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1255+34646T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97100856 | ||||||
| chr8:97101572
|
CTT | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(8): Show | 11 | HG00733.hp2 HG01884.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1255+35380_1255+35 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101572 | |||||
| chr8:97101572
|
CTTT | C | 82 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1255+35379_1255+35 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101572 | |||||
| chr8:97101913
|
GCTCT | G | 71 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0027others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.1255+35729_1255+35 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101913 | |||||
| chr8:97101913
|
GCTCTCTC others(3): Show |
G | 1 | a0001c0002t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255+35723_1255+35 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101913 | |||||
| chr8:97101935
|
T | C | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1255+35725T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97101935 | ||||||
| chr8:97101935
|
TCTCTCTC others(1): Show |
T | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+35729_1255+35 others(14): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101935 | |||||
| chr8:97101937
|
TCTCTCC | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+35731_1255+35 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101937 | |||||
| chr8:97101939
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0070others(12): Show | 15 | HG01261.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255+35729T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97101939 | ||||||
| chr8:97101945
|
T | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+35735T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97101945 | ||||||
| chr8:97101947
|
C | CCTCT | 3 | a0001c0001t0002g0044a0001c0002t0001g0115a0002c0003t0001g0087 | 3 | HG02615.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1255+35740_1255+35 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101947 | |||||
| chr8:97101949
|
TCC | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0004t0001g0107others(1): Show | 4 | NA18522.hp2 NA18949.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255+35741_1255+35 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97101949 | |||||
| chr8:97101951
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(7): Show | 10 | HG01261.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1255+35741C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97101951 | ||||||
| chr8:97101955
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+35745T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97101955 | ||||||
| chr8:97102082
|
G | C | 1 | a0002c0003t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1255+35872G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97102082 | ||||||
| chr8:97102425
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+36215G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97102425 | ||||||
| chr8:97103006
|
C | G | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1255+36796C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97103006 | ||||||
| chr8:97103105
|
A | G | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1255+36895A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97103105 | ||||||
| chr8:97103690
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0028others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255+37480A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97103690 | ||||||
| chr8:97103891
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0033others(46): Show | 49 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1255+37681C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97103891 | ||||||
| chr8:97104036
|
T | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0028others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255+37826T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97104036 | ||||||
| chr8:97104807
|
T | G | 2 | a0001c0002t0001g0025a0001c0002t0002g0050 | 2 | HG01261.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1256-38213T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97104807 | ||||||
| chr8:97104824
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1256-38196G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97104824 | ||||||
| chr8:97104912
|
G | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0002t0001g0079others(5): Show | 8 | HG00099.hp2 HG01943.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-38108G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97104912 | ||||||
| chr8:97105037
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-37983G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97105037 | ||||||
| chr8:97105079
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0002g0044others(3): Show | 6 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-37941G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97105079 | ||||||
| chr8:97105085
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-37935A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97105085 | ||||||
| chr8:97105174
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0041others(1): Show | 4 | HG00733.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-37846G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97105174 | ||||||
| chr8:97105275
|
T | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-37745T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97105275 | ||||||
| chr8:97105430
|
A | G | 1 | a0001c0002t0002g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1256-37590A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97105430 | ||||||
| chr8:97106010
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-37010A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106010 | ||||||
| chr8:97106144
|
T | C | 4 | a0001c0001t0001g0033a0001c0002t0001g0071a0001c0002t0001g0072others(1): Show | 4 | HG02922.hp2 NA18989.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256-36876T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106144 | ||||||
| chr8:97106307
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1256-36713G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106307 | ||||||
| chr8:97106460
|
C | A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-36560C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106460 | ||||||
| chr8:97106498
|
G | T | 95 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1256-36522G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106498 | ||||||
| chr8:97106532
|
A | C | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1256-36488A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106532 | ||||||
| chr8:97106613
|
T | G | 2 | a0001c0002t0001g0005a0002c0003t0001g0118 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1256-36407T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106613 | ||||||
| chr8:97106833
|
C | G | 95 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1256-36187C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97106833 | ||||||
| chr8:97107126
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1256-35894T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97107126 | ||||||
| chr8:97107755
|
G | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0002t0001g0079others(4): Show | 7 | HG00099.hp2 HG01943.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-35265G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97107755 | ||||||
| chr8:97108130
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-34890T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108130 | ||||||
| chr8:97108163
|
T | C | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1256-34857T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108163 | ||||||
| chr8:97108265
|
T | A | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-34755T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108265 | ||||||
| chr8:97108278
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-34742G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108278 | ||||||
| chr8:97108352
|
T | A | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1256-34668T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108352 | ||||||
| chr8:97108360
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-34660G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108360 | ||||||
| chr8:97108575
|
C | T | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-34445C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108575 | ||||||
| chr8:97108672
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1256-34348G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97108672 | ||||||
| chr8:97109188
|
C | A | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-33832C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97109188 | ||||||
| chr8:97109285
|
A | G | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-33735A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97109285 | ||||||
| chr8:97109400
|
G | A | 2 | a0001c0007t0001g0038a0001c0008t0001g0116 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1256-33620G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97109400 | ||||||
| chr8:97109414
|
T | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(27): Show | 30 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256-33606T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97109414 | ||||||
| chr8:97109531
|
C | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-33489C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97109531 | ||||||
| chr8:97109762
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1256-33258G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97109762 | ||||||
| chr8:97110274
|
T | C | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.1256-32746T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110274 | ||||||
| chr8:97110469
|
A | G | 30 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(27): Show | 30 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256-32551A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110469 | ||||||
| chr8:97110494
|
A | G | 37 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0026others(34): Show | 37 | HG00099.hp2 HG01261.hp1 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.1256-32526A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110494 | ||||||
| chr8:97110575
|
T | G | 4 | a0001c0001t0002g0021a0001c0002t0001g0121a0001c0002t0002g0085others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-32445T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110575 | ||||||
| chr8:97110665
|
A | G | 1 | a0002c0003t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1256-32355A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110665 | ||||||
| chr8:97110796
|
T | C | 2 | a0001c0002t0001g0084a0009c0012t0001g0090 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-32224T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110796 | ||||||
| chr8:97110799
|
G | A | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1256-32221G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110799 | ||||||
| chr8:97110996
|
A | G | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-32024A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97110996 | ||||||
| chr8:97111493
|
G | A | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-31527G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97111493 | ||||||
| chr8:97111512
|
G | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1256-31508G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97111512 | ||||||
| chr8:97111845
|
T | C | 2 | a0003c0005t0001g0007a0003c0005t0001g0068 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1256-31175T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97111845 | ||||||
| chr8:97111915
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0026others(11): Show | 14 | HG00099.hp2 HG01943.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.1256-31105T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97111915 | ||||||
| chr8:97112001
|
G | A | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256-31019G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112001 | ||||||
| chr8:97112155
|
T | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-30865T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112155 | ||||||
| chr8:97112162
|
AT | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(60): Show | 63 | HG01081.hp2 HG01261.hp1 HG01516.hp1 others(60): Show |
intron_variant | MODIFIER | c.1256-30847delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97112162 | |||||
| chr8:97112433
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1256-30587G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112433 | ||||||
| chr8:97112538
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1256-30482A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112538 | ||||||
| chr8:97112579
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1256-30441G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112579 | ||||||
| chr8:97112684
|
C | T | 1 | a0001c0002t0002g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1256-30336C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112684 | ||||||
| chr8:97112822
|
G | C | 35 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(32): Show | 35 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.1256-30198G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97112822 | ||||||
| chr8:97113250
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1256-29770G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97113250 | ||||||
| chr8:97113350
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1256-29670G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97113350 | ||||||
| chr8:97113368
|
A | G | 30 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(27): Show | 30 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256-29652A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97113368 | ||||||
| chr8:97113709
|
G | C | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1256-29311G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97113709 | ||||||
| chr8:97114370
|
T | C | 33 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(30): Show | 33 | HG01261.hp1 HG01943.hp1 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.1256-28650T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97114370 | ||||||
| chr8:97114486
|
A | C | 1 | a0002c0003t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1256-28534A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97114486 | ||||||
| chr8:97114608
|
A | T | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-28412A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97114608 | ||||||
| chr8:97114894
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0002g0020a0001c0001t0002g0022 | 3 | HG02572.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1256-28126T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97114894 | ||||||
| chr8:97114909
|
T | C | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-28111T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97114909 | ||||||
| chr8:97115351
|
G | T | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-27669G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115351 | ||||||
| chr8:97115387
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1256-27633A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115387 | ||||||
| chr8:97115530
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1256-27490C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115530 | ||||||
| chr8:97115545
|
A | G | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256-27475A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115545 | ||||||
| chr8:97115554
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077 | 3 | NA18945.hp2 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1256-27466C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115554 | ||||||
| chr8:97115581
|
C | T | 1 | a0008c0011t0002g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1256-27439C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115581 | ||||||
| chr8:97115722
|
C | T | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1256-27298C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115722 | ||||||
| chr8:97115785
|
A | T | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1256-27235A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115785 | ||||||
| chr8:97115812
|
C | T | 1 | a0005c0013t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1256-27208C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115812 | ||||||
| chr8:97115826
|
C | G | 31 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0027others(28): Show | 31 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1256-27194C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115826 | ||||||
| chr8:97115941
|
A | C | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-27079A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97115941 | ||||||
| chr8:97116047
|
G | A | 2 | a0001c0001t0001g0047a0006c0010t0001g0045 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1256-26973G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97116047 | ||||||
| chr8:97116420
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1256-26600A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97116420 | ||||||
| chr8:97116707
|
G | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0042 | 3 | HG00733.hp2 HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1256-26313G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97116707 | ||||||
| chr8:97116926
|
G | A | 43 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG01081.hp2 HG01516.hp1 others(40): Show |
intron_variant | MODIFIER | c.1256-26094G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97116926 | ||||||
| chr8:97117152
|
G | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(27): Show | 30 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256-25868G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97117152 | ||||||
| chr8:97117311
|
A | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0026others(11): Show | 14 | HG00099.hp2 HG01943.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.1256-25709A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97117311 | ||||||
| chr8:97117312
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1256-25708A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97117312 | ||||||
| chr8:97117952
|
C | T | 25 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0061others(22): Show | 25 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.1256-25068C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97117952 | ||||||
| chr8:97117992
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1256-25028T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97117992 | ||||||
| chr8:97118187
|
A | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0002g0044others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256-24833A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97118187 | ||||||
| chr8:97118743
|
C | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(28): Show | 31 | HG01261.hp1 HG01978.hp1 HG02004.hp1 others(28): Show |
intron_variant | MODIFIER | c.1256-24277C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97118743 | ||||||
| chr8:97119052
|
G | A | 1 | a0001c0001t0004g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1256-23968G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97119052 | ||||||
| chr8:97119055
|
G | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(27): Show | 30 | HG01081.hp1 HG01261.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256-23965G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97119055 | ||||||
| chr8:97119121
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1256-23899G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97119121 | ||||||
| chr8:97119185
|
T | A | 4 | a0001c0001t0001g0028a0001c0002t0001g0092a0001c0002t0001g0093others(1): Show | 4 | HG02630.hp2 HG03516.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-23835T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97119185 | ||||||
| chr8:97119264
|
A | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(75): Show | 78 | HG00099.hp2 HG00733.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.1256-23756A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97119264 | ||||||
| chr8:97119328
|
C | CA | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(43): Show | 46 | HG00733.hp2 HG01261.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.1256-23670dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97119328 | |||||
| chr8:97119328
|
C | CAA | 6 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0002t0001g0002others(3): Show | 6 | HG01517.hp2 HG01943.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256-23671_1256-23 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97119328 | |||||
| chr8:97119328
|
CAAAAA | C | 9 | a0001c0001t0002g0021a0001c0002t0001g0005a0001c0002t0001g0006others(6): Show | 9 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1256-23674_1256-23 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97119328 | |||||
| chr8:97119328
|
CAAAAAA | C | 5 | a0001c0001t0001g0026a0001c0002t0001g0079a0001c0002t0001g0111others(2): Show | 5 | HG00099.hp2 HG03195.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-23675_1256-23 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97119328 | |||||
| chr8:97119443
|
T | TA | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(70): Show | 73 | HG00099.hp2 HG00733.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.1256-23563dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97119443 | |||||
| chr8:97119531
|
T | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0002t0001g0079others(4): Show | 7 | HG00099.hp2 HG02965.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256-23489T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97119531 | ||||||
| chr8:97120005
|
C | T | 6 | a0001c0001t0001g0009a0001c0002t0001g0058a0001c0002t0001g0060others(3): Show | 6 | HG02040.hp1 HG03453.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256-23015C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97120005 | ||||||
| chr8:97120010
|
T | C | 2 | a0001c0001t0001g0027a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1256-23010T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97120010 | ||||||
| chr8:97120156
|
C | T | 29 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(26): Show | 29 | HG00733.hp1 HG01081.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1256-22864C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97120156 | ||||||
| chr8:97120282
|
CCAACTCC others(139): Show |
C | 2 | a0001c0001t0002g0044a0001c0002t0002g0039 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1256-22718_1256-22 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97120282 | |||||
| chr8:97120302
|
T | TAGATAAA others(139): Show |
1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1256-22593_1256-22 others(152): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97120302 | |||||
| chr8:97120371
|
CATTCCTT others(9): Show |
C | 4 | a0001c0001t0001g0047a0001c0002t0002g0051a0006c0010t0001g0045others(1): Show | 4 | HG00099.hp1 HG01943.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-22617_1256-22 others(22): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97120371 | |||||
| chr8:97120428
|
A | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(95): Show | 98 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.1256-22592A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97120428 | ||||||
| chr8:97120545
|
T | C | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-22475T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97120545 | ||||||
| chr8:97121119
|
T | TA | 3 | a0001c0001t0001g0063a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-21900dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97121119 | |||||
| chr8:97121245
|
A | C | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1256-21775A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97121245 | ||||||
| chr8:97121790
|
A | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(49): Show | 52 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.1256-21230A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97121790 | ||||||
| chr8:97122213
|
G | A | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-20807G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122213 | ||||||
| chr8:97122215
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1256-20805G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122215 | ||||||
| chr8:97122519
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1256-20501C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122519 | ||||||
| chr8:97122795
|
G | A | 2 | a0001c0002t0001g0098a0004c0006t0001g0075 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1256-20225G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122795 | ||||||
| chr8:97122884
|
C | CAATAA | 2 | a0001c0001t0001g0017a0001c0001t0001g0041 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1256-20094_1256-20 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122884 | |||||
| chr8:97122884
|
CAATAAAA others(3): Show |
C | 16 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0080others(13): Show | 16 | HG01081.hp2 HG01517.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1256-20099_1256-20 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122884 | |||||
| chr8:97122898
|
A | AAAATAAA others(22): Show |
1 | a0001c0002t0001g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1256-20089_1256-20 others(35): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122898 | |||||
| chr8:97122903
|
A | AAAATAAA others(2): Show |
2 | a0001c0007t0001g0038a0004c0006t0001g0074 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1256-20113_1256-20 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122903 | |||||
| chr8:97122912
|
TA | T | 5 | a0001c0002t0001g0091a0001c0004t0001g0107a0001c0008t0001g0116others(2): Show | 5 | HG02647.hp1 HG02965.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-20104delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122912 | |||||
| chr8:97122917
|
TAAAATAA others(8): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1256-20099_1256-20 others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122917 | |||||
| chr8:97122917
|
TAAAATAA others(13): Show |
T | 9 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0019others(6): Show | 9 | HG01884.hp2 HG01975.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1256-20099_1256-20 others(26): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122917 | |||||
| chr8:97122917
|
TAAAATAA others(18): Show |
T | 25 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0031others(22): Show | 25 | HG01978.hp2 HG02040.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1256-20099_1256-20 others(31): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122917 | |||||
| chr8:97122917
|
TAAAATAA others(28): Show |
T | 2 | a0001c0001t0001g0042a0001c0002t0001g0018 | 2 | HG00733.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1256-20099_1256-20 others(41): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122917 | |||||
| chr8:97122918
|
A | AAAAT | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1256-20098_1256-20 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122918 | |||||
| chr8:97122923
|
AAAAT | A | 4 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0008t0001g0116others(1): Show | 4 | HG02647.hp1 HG02965.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256-20089_1256-20 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122923 | |||||
| chr8:97122926
|
A | T | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1256-20094A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122926 | ||||||
| chr8:97122927
|
T | A | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1256-20093T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122927 | ||||||
| chr8:97122927
|
T | TA | 10 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0002t0001g0088others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-20090dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122927 | |||||
| chr8:97122927
|
T | TAAATA | 2 | a0001c0001t0001g0076a0001c0002t0001g0060 | 2 | HG02040.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1256-20043_1256-20 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122927 | |||||
| chr8:97122931
|
T | A | 5 | a0001c0001t0001g0057a0001c0002t0001g0006a0001c0002t0001g0040others(2): Show | 5 | HG00099.hp1 HG01261.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-20089T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122931 | ||||||
| chr8:97122932
|
A | AAAAT | 2 | a0001c0001t0001g0023a0001c0002t0001g0122 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1256-20084_1256-20 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122932 | |||||
| chr8:97122932
|
A | AAAATAAA others(17): Show |
1 | a0001c0002t0001g0066 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1256-20084_1256-20 others(30): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122932 | |||||
| chr8:97122932
|
A | T | 5 | a0001c0001t0001g0057a0001c0002t0001g0006a0001c0002t0001g0040others(2): Show | 5 | HG00099.hp1 HG01261.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-20088A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122932 | ||||||
| chr8:97122956
|
T | TA | 3 | a0001c0001t0001g0080a0001c0001t0001g0112a0001c0002t0001g0088 | 3 | HG02895.hp1 NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1256-20060dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122956 | |||||
| chr8:97122960
|
A | AT | 5 | a0001c0004t0001g0107a0001c0007t0001g0038a0002c0003t0001g0015others(2): Show | 5 | HG02922.hp2 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-20059dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122960 | |||||
| chr8:97122960
|
A | ATAAAAT | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-20059_1256-20 others(12): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122960 | |||||
| chr8:97122961
|
T | TA | 5 | a0001c0002t0001g0049a0001c0002t0001g0058a0001c0002t0001g0069others(2): Show | 5 | HG01081.hp2 NA18949.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-20055dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122961 | |||||
| chr8:97122964
|
A | AAT | 17 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(14): Show | 17 | HG01261.hp1 HG01943.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1256-20054_1256-20 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122964 | |||||
| chr8:97122967
|
AAAAT | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0125others(4): Show | 7 | HG01517.hp2 HG01943.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256-20049_1256-20 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122967 | |||||
| chr8:97122972
|
A | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0104others(1): Show | 4 | HG00733.hp1 HG01255.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256-20048A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122972 | ||||||
| chr8:97122973
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-20047A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122973 | ||||||
| chr8:97122974
|
AATAAAAT others(43): Show |
A | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-20044_1256-19 others(56): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122974 | |||||
| chr8:97122977
|
A | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0030others(16): Show | 19 | HG00099.hp1 HG00733.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1256-20043A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122977 | ||||||
| chr8:97122980
|
AT | A | 35 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0061others(32): Show | 35 | HG00733.hp2 HG01081.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.1256-20038delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122980 | |||||
| chr8:97122981
|
T | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG01255.hp2 HG01516.hp1 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.1256-20039T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122981 | ||||||
| chr8:97122981
|
T | TA | 6 | a0001c0002t0001g0088a0001c0002t0001g0115a0001c0004t0001g0107others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256-20039_1256-20 others(7): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122981 | ||||||
| chr8:97122981
|
TTAAAATA others(2): Show |
T | 2 | a0001c0001t0001g0080a0001c0001t0001g0112 | 2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1256-20038_1256-20 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122981 | ||||||
| chr8:97122986
|
A | T | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1256-20034A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122986 | ||||||
| chr8:97122987
|
TAAA | T | 5 | a0001c0002t0001g0049a0001c0002t0001g0058a0001c0002t0001g0069others(2): Show | 5 | HG01081.hp2 NA18949.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-20031_1256-20 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122987 | |||||
| chr8:97122999
|
A | C | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1256-20021A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122999 | ||||||
| chr8:97122999
|
A | T | 23 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0030others(20): Show | 23 | HG01255.hp2 HG01516.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.1256-20021A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97122999 | ||||||
| chr8:97122999
|
AAAT | A | 18 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG01261.hp1 HG01943.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1256-20019_1256-20 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97122999 | |||||
| chr8:97123000
|
AAT | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0112a0001c0002t0001g0049others(5): Show | 8 | HG01081.hp2 HG02922.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-20016_1256-20 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123000 | |||||
| chr8:97123002
|
T | A | 24 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0030others(21): Show | 24 | HG01255.hp2 HG01516.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.1256-20018T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123002 | ||||||
| chr8:97123002
|
T | TAA | 2 | a0001c0001t0002g0024a0001c0007t0001g0038 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1256-20017_1256-20 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123002 | |||||
| chr8:97123002
|
T | TATAAA | 4 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(1): Show | 4 | HG02630.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-19997_1256-19 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123002 | |||||
| chr8:97123004
|
T | A | 5 | a0001c0002t0001g0115a0001c0004t0001g0107a0002c0003t0001g0015others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256-20016T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123004 | ||||||
| chr8:97123005
|
A | AAT | 5 | a0001c0002t0001g0115a0001c0004t0001g0107a0002c0003t0001g0015others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256-20014_1256-20 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123005 | |||||
| chr8:97123023
|
A | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0030others(34): Show | 37 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(34): Show |
intron_variant | MODIFIER | c.1256-19997A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123023 | ||||||
| chr8:97123024
|
T | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0030others(34): Show | 37 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(34): Show |
intron_variant | MODIFIER | c.1256-19996T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123024 | ||||||
| chr8:97123024
|
T | TA | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(33): Show | 36 | HG00099.hp1 HG01884.hp2 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.1256-19993dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123024 | |||||
| chr8:97123024
|
T | TAAAATAA others(8): Show |
1 | a0001c0001t0001g0063 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1256-19993_1256-19 others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123024 | |||||
| chr8:97123024
|
T | TAAATA | 17 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0034others(14): Show | 17 | HG00099.hp2 HG01081.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1256-19978_1256-19 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123024 | |||||
| chr8:97123024
|
T | TAAATAAA others(3): Show |
3 | a0001c0004t0001g0107a0002c0003t0001g0015a0004c0006t0001g0074 | 3 | HG03225.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1256-19983_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123024 | |||||
| chr8:97123028
|
T | A | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0125others(8): Show | 11 | HG01517.hp2 HG01943.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1256-19992T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123028 | ||||||
| chr8:97123029
|
A | AAAAT | 30 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(27): Show | 30 | HG01884.hp2 HG01975.hp2 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.1256-19987_1256-19 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123029 | |||||
| chr8:97123029
|
A | T | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0125others(8): Show | 11 | HG01517.hp2 HG01943.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1256-19991A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123029 | ||||||
| chr8:97123033
|
TA | T | 2 | a0001c0002t0001g0055a0007c0009t0001g0062 | 2 | HG00099.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-19983delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123033 | |||||
| chr8:97123042
|
A | T | 8 | a0001c0001t0001g0080a0001c0002t0001g0049a0001c0002t0001g0058others(5): Show | 8 | HG01081.hp2 HG03225.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1256-19978A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123042 | ||||||
| chr8:97123043
|
T | A | 8 | a0001c0001t0001g0080a0001c0002t0001g0049a0001c0002t0001g0058others(5): Show | 8 | HG01081.hp2 HG03225.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1256-19977T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123043 | ||||||
| chr8:97123043
|
T | TA | 3 | a0001c0001t0002g0067a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG01255.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-19974dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123043 | |||||
| chr8:97123043
|
T | TAAATAAA others(7): Show |
1 | a0001c0008t0001g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1256-19970_1256-19 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123043 | |||||
| chr8:97123047
|
T | A | 19 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(16): Show | 19 | HG01261.hp1 HG01943.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1256-19973T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123047 | ||||||
| chr8:97123048
|
A | T | 19 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(16): Show | 19 | HG01261.hp1 HG01943.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1256-19972A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123048 | ||||||
| chr8:97123061
|
A | T | 2 | a0001c0001t0001g0031a0001c0002t0001g0088 | 2 | HG02895.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1256-19959A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123061 | ||||||
| chr8:97123062
|
T | A | 2 | a0001c0001t0001g0031a0001c0002t0001g0088 | 2 | HG02895.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1256-19958T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123062 | ||||||
| chr8:97123066
|
A | ATAAAATA others(3): Show |
5 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(2): Show | 5 | HG02630.hp2 HG02965.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-19954_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123066 | ||||||
| chr8:97123066
|
A | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(59): Show | 62 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.1256-19954A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123066 | ||||||
| chr8:97123067
|
A | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0032others(21): Show | 24 | HG00733.hp2 HG01255.hp1 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.1256-19953A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123067 | ||||||
| chr8:97123085
|
T | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0032others(19): Show | 22 | HG01978.hp2 HG02040.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.1256-19935T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123085 | ||||||
| chr8:97123086
|
A | T | 22 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0032others(19): Show | 22 | HG01978.hp2 HG02040.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.1256-19934A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123086 | ||||||
| chr8:97123086
|
AAAATAAA others(7): Show |
A | 2 | a0001c0001t0001g0042a0001c0002t0001g0018 | 2 | HG00733.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1256-19916_1256-19 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123086 | |||||
| chr8:97123100
|
T | TAAATAAA others(8): Show |
1 | a0001c0002t0001g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1256-19907_1256-19 others(21): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123100 | |||||
| chr8:97123100
|
TAAATA | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0080a0001c0002t0001g0049others(7): Show | 10 | HG01081.hp2 HG02615.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1256-19897_1256-19 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123100 | |||||
| chr8:97123104
|
T | A | 65 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(62): Show | 65 | HG01261.hp1 HG01517.hp2 HG01884.hp2 others(62): Show |
intron_variant | MODIFIER | c.1256-19916T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123104 | ||||||
| chr8:97123105
|
A | T | 65 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(62): Show | 65 | HG01261.hp1 HG01517.hp2 HG01884.hp2 others(62): Show |
intron_variant | MODIFIER | c.1256-19915A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123105 | ||||||
| chr8:97123115
|
AAAATAAA others(2): Show |
A | 2 | a0001c0002t0001g0120a0002c0003t0001g0053 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1256-19892_1256-19 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123115 | |||||
| chr8:97123123
|
A | T | 5 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0092others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-19897A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123123 | ||||||
| chr8:97123124
|
T | A | 5 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0092others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-19896T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123124 | ||||||
| chr8:97123128
|
T | A | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01261.hp1 HG01943.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.1256-19892T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123128 | ||||||
| chr8:97123129
|
A | T | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01261.hp1 HG01943.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.1256-19891A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123129 | ||||||
| chr8:97123134
|
A | AAAATAAA others(2): Show |
3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | HG02630.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1256-19882_1256-19 others(15): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123134 | |||||
| chr8:97123143
|
TAAAATAA others(3): Show |
T | 1 | a0002c0003t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1256-19873_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123143 | |||||
| chr8:97123147
|
A | T | 2 | a0001c0001t0001g0042a0001c0002t0001g0018 | 2 | HG00733.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1256-19873A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123147 | ||||||
| chr8:97123148
|
T | A | 2 | a0001c0001t0001g0042a0001c0002t0001g0018 | 2 | HG00733.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1256-19872T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123148 | ||||||
| chr8:97123148
|
TAAATA | T | 61 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(58): Show | 61 | HG01081.hp2 HG01261.hp1 HG01517.hp2 others(58): Show |
intron_variant | MODIFIER | c.1256-19846_1256-19 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123148 | |||||
| chr8:97123148
|
TAAATAAA others(3): Show |
T | 1 | a0001c0002t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1256-19851_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123148 | |||||
| chr8:97123152
|
T | A | 6 | a0001c0001t0001g0047a0001c0001t0002g0067a0001c0002t0001g0092others(3): Show | 6 | HG01255.hp1 HG01943.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-19868T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123152 | ||||||
| chr8:97123153
|
A | AAAATAAA others(7): Show |
4 | a0001c0002t0001g0091a0001c0008t0001g0116a0007c0009t0001g0062others(1): Show | 4 | HG00099.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-19863_1256-19 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123153 | |||||
| chr8:97123153
|
A | AAAATAAA others(115): Show |
1 | a0001c0002t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1256-19844_1256-19 others(128): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123153 | |||||
| chr8:97123153
|
A | T | 6 | a0001c0001t0001g0047a0001c0001t0002g0067a0001c0002t0001g0092others(3): Show | 6 | HG01255.hp1 HG01943.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-19867A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123153 | ||||||
| chr8:97123172
|
TAAAATAT others(3): Show |
T | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1256-19846_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123172 | |||||
| chr8:97123174
|
A | AATAAAAT others(7): Show |
1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1256-19845_1256-19 others(20): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123174 | |||||
| chr8:97123174
|
A | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0002t0001g0040others(4): Show | 7 | HG00099.hp2 HG00733.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-19846A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123174 | ||||||
| chr8:97123177
|
T | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0002t0001g0040others(4): Show | 7 | HG00099.hp2 HG00733.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-19843T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123177 | ||||||
| chr8:97123179
|
T | A | 7 | a0001c0002t0001g0084a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-19841T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123179 | ||||||
| chr8:97123182
|
A | T | 7 | a0001c0002t0001g0084a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-19838A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123182 | ||||||
| chr8:97123204
|
T | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0063others(3): Show | 6 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-19816T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123204 | ||||||
| chr8:97123206
|
A | AAAAAT | 9 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0095others(6): Show | 9 | HG00099.hp1 HG04184.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1256-19785_1256-19 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123206 | |||||
| chr8:97123206
|
A | AAATAAAA others(3): Show |
1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1256-19812_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123206 | |||||
| chr8:97123206
|
A | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0063others(4): Show | 7 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-19814A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123206 | ||||||
| chr8:97123206
|
AAAAAT | A | 4 | a0001c0002t0001g0060a0001c0002t0002g0039a0001c0004t0001g0107others(1): Show | 4 | HG02040.hp1 HG02109.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-19785_1256-19 others(11): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123206 | |||||
| chr8:97123206
|
AAAAATAA others(3): Show |
A | 2 | a0001c0001t0001g0027a0001c0002t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1256-19790_1256-19 others(16): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123206 | |||||
| chr8:97123208
|
AAAT | A | 25 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0031others(22): Show | 25 | HG01081.hp2 HG01978.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.1256-19809_1256-19 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123208 | |||||
| chr8:97123209
|
A | T | 8 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(5): Show | 8 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-19811A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123209 | ||||||
| chr8:97123211
|
T | A | 8 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(5): Show | 8 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-19809T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123211 | ||||||
| chr8:97123614
|
A | G | 10 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(7): Show | 10 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-19406A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123614 | ||||||
| chr8:97123757
|
G | T | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1256-19263G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123757 | ||||||
| chr8:97123760
|
A | C | 1 | a0001c0002t0001g0002 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1256-19260A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123760 | ||||||
| chr8:97123765
|
CA | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0002t0001g0018others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-19247delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97123765 | |||||
| chr8:97123989
|
G | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256-19031G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97123989 | ||||||
| chr8:97124020
|
T | G | 10 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(7): Show | 10 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-19000T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97124020 | ||||||
| chr8:97124026
|
C | G | 10 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(7): Show | 10 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-18994C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97124026 | ||||||
| chr8:97124225
|
C | CA | 35 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0026others(32): Show | 35 | HG00099.hp2 HG01081.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1256-18769dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97124225 | |||||
| chr8:97124225
|
CA | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(40): Show | 43 | HG01081.hp2 HG01884.hp2 HG01943.hp1 others(40): Show |
intron_variant | MODIFIER | c.1256-18769delA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97124225 | |||||
| chr8:97124225
|
CAA | C | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256-18770_1256-18 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97124225 | |||||
| chr8:97124618
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1256-18402T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97124618 | ||||||
| chr8:97124921
|
A | G | 5 | a0001c0001t0001g0061a0001c0001t0002g0100a0001c0002t0001g0002others(2): Show | 5 | HG01517.hp2 HG01975.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-18099A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97124921 | ||||||
| chr8:97124969
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1256-18051C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97124969 | ||||||
| chr8:97124970
|
G | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1256-18050G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97124970 | ||||||
| chr8:97125270
|
A | G | 2 | a0001c0002t0001g0098a0004c0006t0001g0075 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1256-17750A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125270 | ||||||
| chr8:97125438
|
C | T | 2 | a0001c0002t0001g0098a0004c0006t0001g0075 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1256-17582C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125438 | ||||||
| chr8:97125469
|
A | G | 1 | a0002c0003t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1256-17551A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125469 | ||||||
| chr8:97125570
|
G | T | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1256-17450G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125570 | ||||||
| chr8:97125650
|
A | C | 7 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0108others(4): Show | 7 | HG02040.hp2 NA18747.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256-17370A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125650 | ||||||
| chr8:97125652
|
A | G | 1 | a0001c0002t0002g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1256-17368A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125652 | ||||||
| chr8:97125709
|
G | T | 3 | a0001c0001t0001g0063a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-17311G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125709 | ||||||
| chr8:97125983
|
G | A | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-17037G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97125983 | ||||||
| chr8:97126133
|
A | G | 1 | a0009c0012t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1256-16887A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126133 | ||||||
| chr8:97126193
|
G | C | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1256-16827G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126193 | ||||||
| chr8:97126196
|
C | T | 21 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(18): Show | 21 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1256-16824C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126196 | ||||||
| chr8:97126309
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-16711A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126309 | ||||||
| chr8:97126387
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1256-16633C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126387 | ||||||
| chr8:97126538
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1256-16482C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126538 | ||||||
| chr8:97126688
|
T | A | 1 | a0001c0002t0001g0069 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1256-16332T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126688 | ||||||
| chr8:97126758
|
T | A | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1256-16262T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126758 | ||||||
| chr8:97126894
|
A | G | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1256-16126A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97126894 | ||||||
| chr8:97127100
|
C | A | 1 | a0004c0006t0001g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256-15920C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97127100 | ||||||
| chr8:97127193
|
T | C | 3 | a0001c0001t0001g0010a0001c0002t0001g0115a0002c0003t0001g0087 | 3 | HG02615.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-15827T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97127193 | ||||||
| chr8:97127650
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1256-15370C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97127650 | ||||||
| chr8:97127662
|
G | A | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-15358G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97127662 | ||||||
| chr8:97127794
|
T | C | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-15226T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97127794 | ||||||
| chr8:97128035
|
C | T | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-14985C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97128035 | ||||||
| chr8:97128036
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1256-14984G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97128036 | ||||||
| chr8:97128242
|
T | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(49): Show | 52 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.1256-14778T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97128242 | ||||||
| chr8:97128536
|
TTAGCCAG others(6): Show |
T | 1 | a0001c0001t0001g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1256-14479_1256-14 others(19): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97128536 | |||||
| chr8:97128763
|
C | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(49): Show | 52 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.1256-14257C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97128763 | ||||||
| chr8:97128839
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1256-14181G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97128839 | ||||||
| chr8:97129165
|
T | C | 3 | a0001c0001t0001g0063a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-13855T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97129165 | ||||||
| chr8:97129343
|
T | C | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-13677T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97129343 | ||||||
| chr8:97129415
|
G | C | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1256-13605G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97129415 | ||||||
| chr8:97129616
|
C | T | 2 | a0001c0002t0001g0098a0004c0006t0001g0075 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1256-13404C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97129616 | ||||||
| chr8:97129617
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1256-13403G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97129617 | ||||||
| chr8:97129784
|
T | A | 9 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(6): Show | 9 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256-13236T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97129784 | ||||||
| chr8:97130019
|
G | C | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-13001G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130019 | ||||||
| chr8:97130317
|
G | A | 5 | a0001c0001t0001g0061a0001c0001t0002g0100a0001c0002t0001g0002others(2): Show | 5 | HG01517.hp2 HG01975.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1256-12703G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130317 | ||||||
| chr8:97130420
|
GT | G | 30 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(27): Show | 30 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1256-12578delT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97130420 | |||||
| chr8:97130420
|
GTT | G | 17 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0033others(14): Show | 17 | HG01517.hp2 HG01943.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1256-12579_1256-12 others(8): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97130420 | |||||
| chr8:97130420
|
GTTT | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0002t0001g0005others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-12580_1256-12 others(9): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97130420 | |||||
| chr8:97130420
|
GTTTT | G | 23 | a0001c0001t0001g0042a0001c0001t0002g0011a0001c0001t0002g0012others(20): Show | 23 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1256-12581_1256-12 others(10): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97130420 | |||||
| chr8:97130431
|
T | G | 9 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(6): Show | 9 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256-12589T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130431 | ||||||
| chr8:97130432
|
T | G | 1 | a0001c0002t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1256-12588T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130432 | ||||||
| chr8:97130441
|
T | C | 3 | a0001c0001t0001g0063a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-12579T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130441 | ||||||
| chr8:97130442
|
T | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0125others(5): Show | 8 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-12578T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130442 | ||||||
| chr8:97130702
|
A | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(52): Show | 55 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(52): Show |
intron_variant | MODIFIER | c.1256-12318A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130702 | ||||||
| chr8:97130864
|
G | C | 9 | a0001c0001t0001g0026a0001c0002t0001g0060a0001c0002t0001g0065others(6): Show | 9 | HG00099.hp2 HG02040.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1256-12156G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97130864 | ||||||
| chr8:97130900
|
C | CA | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.1256-12109dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97130900 | |||||
| chr8:97131385
|
G | A | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-11635G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131385 | ||||||
| chr8:97131442
|
A | T | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-11578A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131442 | ||||||
| chr8:97131491
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1256-11529C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131491 | ||||||
| chr8:97131591
|
C | G | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-11429C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131591 | ||||||
| chr8:97131684
|
C | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0019others(14): Show | 17 | HG01517.hp2 HG01884.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1256-11336C>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131684 | ||||||
| chr8:97131731
|
C | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(75): Show | 78 | HG00733.hp2 HG01081.hp2 HG01255.hp1 others(75): Show |
intron_variant | MODIFIER | c.1256-11289C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131731 | ||||||
| chr8:97131870
|
C | T | 9 | a0001c0001t0001g0026a0001c0002t0001g0060a0001c0002t0001g0065others(6): Show | 9 | HG00099.hp2 HG02040.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1256-11150C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131870 | ||||||
| chr8:97131910
|
G | GT | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-11104dupT | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97131910 | |||||
| chr8:97131966
|
G | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(85): Show | 88 | HG00733.hp2 HG01081.hp2 HG01255.hp1 others(85): Show |
intron_variant | MODIFIER | c.1256-11054G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97131966 | ||||||
| chr8:97132556
|
G | A | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-10464G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97132556 | ||||||
| chr8:97133034
|
A | C | 3 | a0001c0001t0001g0010a0001c0002t0001g0115a0002c0003t0001g0087 | 3 | HG02615.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-9986A>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97133034 | ||||||
| chr8:97133126
|
G | C | 3 | a0001c0001t0001g0010a0001c0002t0001g0115a0002c0003t0001g0087 | 3 | HG02615.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-9894G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97133126 | ||||||
| chr8:97133170
|
T | C | 3 | a0001c0001t0001g0063a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-9850T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97133170 | ||||||
| chr8:97133502
|
G | A | 4 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(1): Show | 4 | HG02630.hp2 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-9518G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97133502 | ||||||
| chr8:97134416
|
C | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(49): Show | 52 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(49): Show |
intron_variant | MODIFIER | c.1256-8604C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97134416 | ||||||
| chr8:97134462
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1256-8558C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97134462 | ||||||
| chr8:97134516
|
C | A | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256-8504C>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97134516 | ||||||
| chr8:97134883
|
G | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0125a0001c0002t0001g0115others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256-8137G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97134883 | ||||||
| chr8:97135040
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1256-7980T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97135040 | ||||||
| chr8:97135087
|
C | T | 10 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(7): Show | 10 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-7933C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97135087 | ||||||
| chr8:97135311
|
T | C | 51 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(48): Show | 51 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(48): Show |
intron_variant | MODIFIER | c.1256-7709T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97135311 | ||||||
| chr8:97135973
|
T | TG | 2 | a0001c0001t0001g0009a0002c0003t0001g0008 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1256-7046dupG | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97135973 | |||||
| chr8:97136625
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1256-6395G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97136625 | ||||||
| chr8:97137153
|
C | T | 9 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(6): Show | 9 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256-5867C>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97137153 | ||||||
| chr8:97137297
|
T | C | 1 | a0007c0009t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1256-5723T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97137297 | ||||||
| chr8:97137326
|
A | T | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-5694A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97137326 | ||||||
| chr8:97137578
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256-5442A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97137578 | ||||||
| chr8:97137625
|
G | A | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1256-5395G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97137625 | ||||||
| chr8:97137887
|
C | CA | 20 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(17): Show | 20 | HG01255.hp1 HG01261.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1256-5121dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97137887 | |||||
| chr8:97138266
|
T | A | 4 | a0001c0001t0001g0061a0001c0001t0002g0100a0001c0002t0001g0059others(1): Show | 4 | HG01975.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-4754T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97138266 | ||||||
| chr8:97138375
|
G | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0108 | 2 | HG00099.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1256-4645G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97138375 | ||||||
| chr8:97138739
|
G | A | 63 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0023others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1256-4281G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97138739 | ||||||
| chr8:97138796
|
A | G | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-4224A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97138796 | ||||||
| chr8:97138896
|
G | C | 8 | a0001c0001t0001g0026a0001c0002t0001g0065a0001c0002t0001g0066others(5): Show | 8 | HG00099.hp2 NA18945.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.1256-4124G>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97138896 | ||||||
| chr8:97139010
|
T | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG01081.hp1 HG01255.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-4010T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97139010 | ||||||
| chr8:97139067
|
A | G | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1256-3953A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97139067 | ||||||
| chr8:97140012
|
T | TA | 53 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(50): Show | 53 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(50): Show |
intron_variant | MODIFIER | c.1256-2998dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97140012 | |||||
| chr8:97140171
|
G | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0019others(16): Show | 19 | HG01517.hp2 HG01884.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.1256-2849G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140171 | ||||||
| chr8:97140292
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1256-2728T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140292 | ||||||
| chr8:97140297
|
T | C | 21 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(18): Show | 21 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1256-2723T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140297 | ||||||
| chr8:97140367
|
T | TA | 54 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(51): Show | 54 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(51): Show |
intron_variant | MODIFIER | c.1256-2645dupA | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97140367 | |||||
| chr8:97140674
|
T | C | 10 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(7): Show | 10 | HG02630.hp2 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256-2346T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140674 | ||||||
| chr8:97140715
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1256-2305T>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140715 | ||||||
| chr8:97140740
|
A | G | 1 | a0002c0003t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1256-2280A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140740 | ||||||
| chr8:97140789
|
G | T | 2 | a0001c0002t0001g0115a0002c0003t0001g0087 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1256-2231G>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140789 | ||||||
| chr8:97140990
|
A | T | 1 | a0001c0002t0001g0079 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1256-2030A>T | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97140990 | ||||||
| chr8:97141053
|
A | G | 54 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(51): Show | 54 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(51): Show |
intron_variant | MODIFIER | c.1256-1967A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97141053 | ||||||
| chr8:97141150
|
CAT | C | 3 | a0001c0001t0001g0042a0001c0002t0001g0018a0001c0002t0001g0084 | 3 | HG00733.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1256-1868_1256-186 others(6): Show |
CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 97141150 | |||||
| chr8:97141387
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1256-1633A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97141387 | ||||||
| chr8:97141945
|
T | C | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1256-1075T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97141945 | ||||||
| chr8:97142213
|
A | G | 3 | a0001c0001t0001g0063a0001c0002t0001g0055a0007c0009t0001g0062 | 3 | HG00099.hp1 HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1256-807A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97142213 | ||||||
| chr8:97142411
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(42): Show | 45 | HG01081.hp2 HG01517.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.1256-609G>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97142411 | ||||||
| chr8:97142553
|
T | C | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(19): Show | 22 | HG01255.hp1 HG01261.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1256-467T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97142553 | ||||||
| chr8:97142643
|
A | G | 54 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(51): Show | 54 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(51): Show |
intron_variant | MODIFIER | c.1256-377A>G | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97142643 | ||||||
| chr8:97142680
|
T | C | 55 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(52): Show | 55 | HG00733.hp2 HG01081.hp2 HG01517.hp2 others(52): Show |
intron_variant | MODIFIER | c.1256-340T>C | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97142680 | ||||||
| chr8:97142694
|
T | A | 1 | a0002c0003t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1256-326T>A | CPQ | ENSG00000104324.16 | transcript | ENST00000220763.10 | protein_coding | 7/7 | chr8 | 97142694 |