Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10087 |
|---|---|
| ensemblid | ENSG00000113163.19 |
| hgncid | 2205 |
| symbol | CERT1 |
| name | ceramide transporter 1 |
| refseq_nuc | NM_001379029.1 |
| refseq_prot | NP_001365958.1 |
| ensembl_nuc | ENST00000643780.2 |
| ensembl_prot | ENSP00000495760.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 75377775 |
| end | 75511629 |
| strand | - |
| ver | v1.2 |
| region | chr5:75377775-75511629 |
| region5000 | chr5:75372775-75516629 |
| regionname0 | CERT1_chr5_75377775_75511629 |
| regionname5000 | CERT1_chr5_75372775_75516629 |
| 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 | 624 | 334 | 89 | 54 | 147 | 8 | 34 | 113 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0002 | 0/0 | 624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0003 | 0/0 | 624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| 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 | 1/1 | 1875 | 205 | 71 | 37 | 76 | 6 | 13 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| c0002 | 0/0 | 1875 | 126 | 17 | 16 | 70 | 2 | 21 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| c0003 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| c0004 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| c0005 | 0/0 | 1875 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| c0006 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| c0007 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| 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 | 0/0 | 1994 | 118 | 26 | 15 | 56 | 2 | 19 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0002 | 1/1 | 1994 | 115 | 8 | 20 | 69 | 5 | 11 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0003 | 0/0 | 1994 | 34 | 28 | 6 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0004 | 0/0 | 1994 | 12 | 1 | 2 | 8 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0005 | 0/0 | 1994 | 11 | 8 | 3 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0006 | 0/0 | 1994 | 8 | 8 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0007 | 0/0 | 1994 | 6 | 0 | 2 | 4 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0008 | 0/0 | 1994 | 6 | 2 | 2 | 0 | 1 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0009 | 0/0 | 1994 | 6 | 0 | 0 | 6 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0010 | 0/0 | 1994 | 3 | 1 | 1 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0011 | 0/0 | 1994 | 3 | 0 | 0 | 3 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0012 | 0/0 | 1994 | 2 | 2 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0013 | 0/0 | 1994 | 2 | 2 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0014 | 0/0 | 1994 | 2 | 1 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0015 | 0/0 | 1994 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0016 | 0/0 | 1994 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0017 | 0/0 | 1994 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0018 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0019 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0020 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0021 | 0/0 | 1994 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| t0022 | 0/0 | 1994 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| 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 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| 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 | 1/1 | 1875 | 205 | 71 | 37 | 76 | 6 | 13 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002 | 0/0 | 1875 | 126 | 17 | 16 | 70 | 2 | 21 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0005 | 0/0 | 1875 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0006 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0007 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0002c0003 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0003c0004 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3868 | 14 | 13 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0002 | 1/1 | 3868 | 113 | 8 | 19 | 68 | 5 | 11 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0003 | 0/0 | 3868 | 33 | 27 | 6 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0005 | 0/0 | 3868 | 11 | 8 | 3 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0006 | 0/0 | 3868 | 7 | 7 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0007 | 0/0 | 3868 | 6 | 0 | 2 | 4 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0008 | 0/0 | 3868 | 6 | 2 | 2 | 0 | 1 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0010 | 0/0 | 3868 | 3 | 1 | 1 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0011 | 0/0 | 3868 | 3 | 0 | 0 | 3 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0012 | 0/0 | 3868 | 2 | 2 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0013 | 0/0 | 3868 | 2 | 2 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0014 | 0/0 | 3868 | 2 | 1 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0015 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0016 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0001t0017 | 0/0 | 3868 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0001 | 0/0 | 3868 | 103 | 13 | 14 | 55 | 2 | 19 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0004 | 0/0 | 3868 | 12 | 1 | 2 | 8 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0009 | 0/0 | 3868 | 6 | 0 | 0 | 6 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0018 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0019 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0020 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0021 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0002t0022 | 0/0 | 3868 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0005t0002 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0006t0006 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0001c0007t0001 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0002c0003t0002 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| a0003c0004t0003 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | copy fasta | chr5 | 75372775 | 75516629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0008g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0011g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0014g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0015g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0016g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0001t0017g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0009g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0009g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0009g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0009g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0009g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0018g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0021g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0002t0022g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0005t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0006t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0001c0007t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0002c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| a0003c0004t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0249 | EUR | GBR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | GBR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0188 | EUR | GBR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0047 | EUR | GBR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0087 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00642 | hp2 | a0001 | c0005 | t0002 | g0137 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0228 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01081 | hp2 | a0001 | c0001 | t0014 | g0237 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0276 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0334 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0332 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0029 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01361 | hp2 | a0001 | c0001 | t0015 | g0004 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0261 | EUR | IBS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | IBS | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0238 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0262 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0267 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0002 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02027 | hp1 | a0001 | c0002 | t0009 | g0324 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02056 | hp1 | a0001 | c0002 | t0009 | g0323 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02071 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02132 | hp1 | a0001 | c0002 | t0009 | g0328 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02132 | hp2 | a0001 | c0002 | t0021 | g0077 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02135 | hp1 | a0001 | c0002 | t0009 | g0327 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0053 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0333 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | CDX | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CDX | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0258 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02300 | hp1 | a0001 | c0001 | t0016 | g0263 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0195 | AMR | PEL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02622 | hp2 | a0001 | c0006 | t0006 | g0268 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0243 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0018 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02723 | hp1 | a0001 | c0002 | t0018 | g0015 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0241 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ESN | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03579 | hp1 | a0003 | c0004 | t0003 | g0179 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03579 | hp2 | a0001 | c0002 | t0019 | g0006 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03654 | hp1 | a0001 | c0001 | t0017 | g0253 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03654 | hp2 | a0001 | c0002 | t0022 | g0014 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0309 | SAS | BEB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | BEB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0100 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0089 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | STU | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | YRI | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | YRI | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | CHB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | CHB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | YRI | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18959 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18962 | hp1 | a0001 | c0002 | t0009 | g0325 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18975 | hp1 | a0001 | c0007 | t0001 | g0336 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18984 | hp1 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0161 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19001 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | LWK | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | LWK | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | LWK | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | LWK | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19058 | hp2 | a0002 | c0003 | t0002 | g0129 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19063 | hp2 | a0001 | c0002 | t0009 | g0326 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19065 | hp2 | a0001 | c0001 | t0011 | g0230 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19070 | hp2 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | YRI | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0240 | AFR | YRI | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | ASW | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ASW | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | GIH | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | GIH | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02486 | hp1 | a0001 | c0002 | t0020 | g0007 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ACB | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | MSL | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0266 | AFR | USA | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | USA | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | USA | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0308 | AFR | USA | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | LWK | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | LWK | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0174 | REF | REF | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0283 | REF | REF | CERT1_chr5_75372775_75516629 | CERT1 | chr5 | 75372775 | 75516629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75379457
|
C | A | 1 | a0002 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1764G>T | p.Trp588Cys | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 2186/3868 | 1764/1875 | 588/624 | chr5 | 75379457 | ||
| chr5:75416889
|
T | C | 1 | a0003 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.824A>G | p.Lys275Arg | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/17 | 1246/3868 | 824/1875 | 275/624 | chr5 | 75416889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75385948
|
T | C | 2 | a0001c0002a0001c0007 | 127 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(124): Show |
synonymous_variant | LOW | c.1371A>G | p.Glu457Glu | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/17 | 1793/3868 | 1371/1875 | 457/624 | chr5 | 75385948 | ||
| chr5:75426377
|
T | C | 1 | a0001c0005 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.450A>G | p.Ser150Ser | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/17 | 872/3868 | 450/1875 | 150/624 | chr5 | 75426377 | ||
| chr5:75506059
|
G | A | 1 | a0001c0006 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.154C>T | p.Leu52Leu | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/17 | 576/3868 | 154/1875 | 52/624 | chr5 | 75506059 | ||
| chr5:75511118
|
G | A | 1 | a0001c0007 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.90C>T | p.Leu30Leu | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/17 | 512/3868 | 90/1875 | 30/624 | chr5 | 75511118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75377847
|
C | T | 1 | a0001c0001t0013 | 2 | HG02258.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1499G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1499 | chr5 | 75377847 | |||||
| chr5:75377882
|
A | G | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(6): Show | 128 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1464T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1464 | chr5 | 75377882 | |||||
| chr5:75377891
|
G | A | 1 | a0001c0001t0007 | 6 | HG00735.hp2 HG02165.hp1 HG02300.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1455C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1455 | chr5 | 75377891 | |||||
| chr5:75378086
|
T | C | 1 | a0001c0002t0021 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1260 | chr5 | 75378086 | |||||
| chr5:75378121
|
A | C | 1 | a0001c0001t0017 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1225T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1225 | chr5 | 75378121 | |||||
| chr5:75378189
|
G | A | 2 | a0001c0001t0008a0001c0001t0016 | 7 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1157C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1157 | chr5 | 75378189 | |||||
| chr5:75378313
|
G | A | 1 | a0001c0002t0009 | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1033 | chr5 | 75378313 | |||||
| chr5:75378316
|
A | G | 2 | a0001c0002t0019a0001c0002t0020 | 2 | HG02486.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1030T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1030 | chr5 | 75378316 | |||||
| chr5:75378329
|
A | G | 1 | a0001c0001t0016 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1017T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 1017 | chr5 | 75378329 | |||||
| chr5:75378434
|
T | C | 1 | a0001c0002t0009 | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*912A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 912 | chr5 | 75378434 | |||||
| chr5:75378615
|
T | G | 1 | a0001c0002t0022 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 731 | chr5 | 75378615 | |||||
| chr5:75378729
|
G | A | 1 | a0001c0002t0009 | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*617C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 617 | chr5 | 75378729 | |||||
| chr5:75378777
|
A | T | 1 | a0001c0002t0018 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 569 | chr5 | 75378777 | |||||
| chr5:75379099
|
T | C | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(10): Show | 177 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*247A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 247 | chr5 | 75379099 | |||||
| chr5:75379114
|
T | C | 1 | a0001c0002t0009 | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*232A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 232 | chr5 | 75379114 | |||||
| chr5:75379139
|
G | A | 3 | a0001c0001t0006a0001c0001t0014a0001c0006t0006 | 10 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 207 | chr5 | 75379139 | |||||
| chr5:75379150
|
T | C | 10 | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(7): Show | 141 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 196 | chr5 | 75379150 | |||||
| chr5:75379251
|
T | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(15): Show | 200 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*95A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 17/17 | 95 | chr5 | 75379251 | |||||
| chr5:75511278
|
C | T | 1 | a0001c0001t0015 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/17 | 71 | chr5 | 75511278 | |||||
| chr5:75511291
|
C | T | 1 | a0001c0001t0010 | 3 | HG02004.hp1 HG02071.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-84G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/17 | 84 | chr5 | 75511291 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:75379526
|
T | A | 1 | a0002c0003t0002g0129 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1748-53A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75379526 | ||||||
| chr5:75379830
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-357C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75379830 | ||||||
| chr5:75379892
|
T | G | 41 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1748-419A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75379892 | ||||||
| chr5:75380136
|
T | C | 1 | a0001c0001t0005g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1748-663A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380136 | ||||||
| chr5:75380140
|
G | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1748-667C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380140 | ||||||
| chr5:75380268
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-795T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380268 | ||||||
| chr5:75380270
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1748-797T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380270 | ||||||
| chr5:75380279
|
G | A | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1747+793C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380279 | ||||||
| chr5:75380342
|
C | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1747+730G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380342 | ||||||
| chr5:75380440
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1747+632A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380440 | ||||||
| chr5:75380458
|
T | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1747+614A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380458 | ||||||
| chr5:75380514
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1747+558G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380514 | ||||||
| chr5:75380581
|
G | A | 1 | a0001c0006t0006g0268 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1747+491C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380581 | ||||||
| chr5:75380668
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1747+404T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380668 | ||||||
| chr5:75380710
|
G | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | NA18953.hp1 NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1747+362C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380710 | ||||||
| chr5:75380777
|
C | CA | 163 | a0001c0001t0001g0036a0001c0001t0001g0321a0001c0001t0002g0122others(160): Show | 163 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.1747+294dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380777 | ||||||
| chr5:75380777
|
C | CAA | 12 | a0001c0002t0001g0011a0001c0002t0001g0057a0001c0002t0001g0081others(9): Show | 12 | HG01934.hp2 HG02027.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1747+293_1747+294d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380777 | ||||||
| chr5:75380905
|
T | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1747+167A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380905 | ||||||
| chr5:75380998
|
T | G | 35 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(32): Show | 35 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1747+74A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 16/16 | chr5 | 75380998 | ||||||
| chr5:75381238
|
A | G | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1618-37T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381238 | ||||||
| chr5:75381345
|
C | G | 8 | a0001c0001t0002g0265a0001c0001t0008g0261a0001c0001t0008g0262others(5): Show | 8 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618-144G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381345 | ||||||
| chr5:75381399
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-198G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381399 | ||||||
| chr5:75381524
|
TA | T | 31 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0133others(28): Show | 31 | HG00642.hp1 HG01169.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.1618-324delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381524 | ||||||
| chr5:75381540
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-339T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381540 | ||||||
| chr5:75381595
|
A | C | 1 | a0001c0001t0003g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1617+354T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381595 | ||||||
| chr5:75381631
|
G | C | 1 | a0001c0001t0002g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1617+318C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 15/16 | chr5 | 75381631 | ||||||
| chr5:75382158
|
A | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489-81T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75382158 | ||||||
| chr5:75382272
|
G | A | 12 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1489-195C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75382272 | ||||||
| chr5:75382660
|
G | T | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1489-583C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75382660 | ||||||
| chr5:75382743
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1489-666C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75382743 | ||||||
| chr5:75382931
|
G | T | 1 | a0001c0002t0001g0011 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1489-854C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75382931 | ||||||
| chr5:75383050
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1489-973T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383050 | ||||||
| chr5:75383112
|
G | A | 123 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(120): Show | 123 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1489-1035C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383112 | ||||||
| chr5:75383161
|
T | C | 1 | a0001c0002t0018g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1489-1084A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383161 | ||||||
| chr5:75383230
|
T | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1489-1153A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383230 | ||||||
| chr5:75383702
|
C | CAATT | 40 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1488+939_1488+940i others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383702 | ||||||
| chr5:75383741
|
T | A | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1488+901A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383741 | ||||||
| chr5:75383741
|
T | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1488+901A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75383741 | ||||||
| chr5:75384406
|
A | T | 2 | a0001c0001t0014g0237a0001c0001t0014g0238 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1488+236T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75384406 | ||||||
| chr5:75384435
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1488+207C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 14/16 | chr5 | 75384435 | ||||||
| chr5:75385146
|
A | G | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1418-434T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385146 | ||||||
| chr5:75385147
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1418-435C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385147 | ||||||
| chr5:75385173
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1418-461T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385173 | ||||||
| chr5:75385417
|
G | C | 1 | a0001c0002t0004g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1417+485C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385417 | ||||||
| chr5:75385528
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1417+374G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385528 | ||||||
| chr5:75385675
|
C | A | 122 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(119): Show | 122 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1417+227G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385675 | ||||||
| chr5:75385738
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+164A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 13/16 | chr5 | 75385738 | ||||||
| chr5:75386052
|
C | T | 1 | a0001c0001t0006g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1285-18G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386052 | ||||||
| chr5:75386115
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-81G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386115 | ||||||
| chr5:75386138
|
G | T | 5 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285-104C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386138 | ||||||
| chr5:75386149
|
G | T | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1285-115C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386149 | ||||||
| chr5:75386186
|
T | G | 1 | a0001c0001t0001g0319 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1285-152A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386186 | ||||||
| chr5:75386316
|
C | CCAAA | 41 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1285-283_1285-282i others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386316 | ||||||
| chr5:75386477
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1285-443T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386477 | ||||||
| chr5:75386558
|
G | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0035 | 2 | HG03490.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1285-524C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386558 | ||||||
| chr5:75386649
|
T | C | 1 | a0001c0001t0008g0261 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1285-615A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386649 | ||||||
| chr5:75386775
|
A | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0094a0001c0002t0001g0095others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-741T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386775 | ||||||
| chr5:75386786
|
C | T | 6 | a0001c0002t0001g0028a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG02040.hp2 HG03490.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1285-752G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386786 | ||||||
| chr5:75386841
|
G | T | 1 | a0001c0001t0003g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1285-807C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386841 | ||||||
| chr5:75386907
|
G | C | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1285-873C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386907 | ||||||
| chr5:75386928
|
C | T | 1 | a0001c0002t0001g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1285-894G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386928 | ||||||
| chr5:75386946
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1285-912G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386946 | ||||||
| chr5:75386988
|
T | C | 33 | a0001c0001t0002g0143a0001c0002t0001g0088a0001c0002t0001g0089others(30): Show | 33 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.1285-954A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75386988 | ||||||
| chr5:75387006
|
T | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-972A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387006 | ||||||
| chr5:75387013
|
G | A | 2 | a0001c0001t0003g0301a0001c0001t0003g0303 | 2 | HG00642.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1285-979C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387013 | ||||||
| chr5:75387024
|
C | T | 1 | a0001c0001t0012g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1285-990G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387024 | ||||||
| chr5:75387075
|
G | A | 72 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1285-1041C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387075 | ||||||
| chr5:75387079
|
A | G | 127 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(124): Show | 127 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1285-1045T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387079 | ||||||
| chr5:75387239
|
C | G | 1 | a0001c0002t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1285-1205G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387239 | ||||||
| chr5:75387458
|
CAGGCCAG others(3): Show |
C | 1 | a0001c0002t0001g0064 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1285-1434_1285-142 others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387458 | ||||||
| chr5:75387481
|
C | T | 4 | a0001c0001t0002g0188a0001c0001t0002g0202a0001c0001t0002g0249others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-1447G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387481 | ||||||
| chr5:75387507
|
C | A | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1285-1473G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387507 | ||||||
| chr5:75387630
|
T | C | 69 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(66): Show | 69 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1285-1596A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387630 | ||||||
| chr5:75387751
|
GA | G | 8 | a0001c0001t0002g0252a0001c0002t0001g0118a0001c0002t0009g0323others(5): Show | 8 | HG01069.hp2 HG02027.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1718delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387751 | ||||||
| chr5:75387821
|
T | C | 171 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(168): Show | 171 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.1284+1771A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75387821 | ||||||
| chr5:75388066
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1284+1526G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388066 | ||||||
| chr5:75388094
|
C | A | 5 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284+1498G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388094 | ||||||
| chr5:75388318
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+1274C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388318 | ||||||
| chr5:75388537
|
C | T | 1 | a0001c0002t0001g0033 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1284+1055G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388537 | ||||||
| chr5:75388567
|
A | C | 1 | a0001c0001t0002g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1284+1025T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388567 | ||||||
| chr5:75388590
|
G | GCATGCAT others(56): Show |
1 | a0001c0002t0001g0104 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1284+1001_1284+100 others(67): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388590 | ||||||
| chr5:75388595
|
CATGCATA others(21): Show |
C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+969_1284+996d others(30): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388595 | ||||||
| chr5:75388599
|
C | CAT | 13 | a0001c0001t0002g0185a0001c0001t0002g0218a0001c0001t0002g0220others(10): Show | 13 | HG01123.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1284+991_1284+992d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATAT | 12 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0194others(9): Show | 12 | HG00099.hp1 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1284+989_1284+992d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(1): Show |
6 | a0001c0001t0002g0133a0001c0001t0002g0190a0001c0001t0006g0134others(3): Show | 6 | HG02040.hp1 HG02300.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284+985_1284+992d others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(3): Show |
3 | a0001c0001t0002g0193a0001c0001t0002g0239a0001c0001t0006g0256 | 3 | HG03195.hp2 NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1284+983_1284+992d others(12): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(5): Show |
3 | a0001c0001t0002g0269a0001c0001t0003g0293a0001c0001t0007g0226 | 3 | HG01515.hp1 HG02055.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1284+981_1284+992d others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(7): Show |
3 | a0001c0001t0002g0201a0001c0001t0003g0296a0001c0001t0007g0228 | 3 | HG00735.hp2 HG02886.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1284+979_1284+992d others(16): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(9): Show |
1 | a0001c0001t0002g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1284+977_1284+992d others(18): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(70): Show |
1 | a0001c0002t0001g0112 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(79): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(66): Show |
1 | a0001c0002t0001g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(75): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(62): Show |
3 | a0001c0002t0001g0105a0001c0002t0001g0106a0001c0002t0001g0116 | 3 | HG01358.hp2 NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1284+992_1284+993i others(71): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(70): Show |
1 | a0001c0002t0001g0113 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(79): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(60): Show |
4 | a0001c0002t0001g0092a0001c0002t0001g0099a0001c0002t0001g0101others(1): Show | 4 | HG01516.hp2 HG02602.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+992_1284+993i others(69): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(62): Show |
3 | a0001c0002t0001g0100a0001c0002t0001g0107a0001c0002t0001g0111 | 3 | HG03927.hp1 HG04199.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1284+992_1284+993i others(71): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(123): Show |
1 | a0001c0002t0001g0109 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1284+992_1284+993i others(132): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(60): Show |
2 | a0001c0002t0001g0102a0001c0002t0001g0108 | 2 | NA18991.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1284+992_1284+993i others(69): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(56): Show |
1 | a0001c0002t0001g0117 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(65): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(60): Show |
1 | a0001c0002t0001g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(69): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(62): Show |
1 | a0001c0002t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1284+992_1284+993i others(71): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(56): Show |
1 | a0001c0007t0001g0336 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1284+992_1284+993i others(65): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(58): Show |
1 | a0001c0002t0001g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(67): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(58): Show |
1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1284+992_1284+993i others(67): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(50): Show |
1 | a0001c0002t0001g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(59): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(52): Show |
1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1284+992_1284+993i others(61): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(60): Show |
2 | a0001c0002t0001g0095a0001c0002t0001g0096 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1284+992_1284+993i others(69): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(56): Show |
1 | a0001c0002t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(65): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(62): Show |
1 | a0001c0002t0001g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(71): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(38): Show |
1 | a0001c0002t0001g0093 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(47): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
C | CATATATA others(18): Show |
1 | a0001c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1284+992_1284+993i others(27): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CAT | C | 29 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(26): Show | 29 | HG00099.hp2 HG00621.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1284+991_1284+992d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATAT | C | 30 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0130others(27): Show | 30 | HG00544.hp1 HG00597.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1284+989_1284+992d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATAT | C | 8 | a0001c0001t0002g0144a0001c0001t0002g0157a0001c0001t0002g0169others(5): Show | 8 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284+987_1284+992d others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(1): Show |
C | 13 | a0001c0001t0002g0139a0001c0001t0002g0142a0001c0001t0002g0145others(10): Show | 13 | HG00673.hp2 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1284+985_1284+992d others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(3): Show |
C | 24 | a0001c0001t0002g0127a0001c0001t0002g0136a0001c0001t0002g0138others(21): Show | 24 | HG01515.hp2 HG01934.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.1284+983_1284+992d others(12): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0002g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1284+981_1284+992d others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(9): Show |
C | 8 | a0001c0001t0013g0243a0001c0001t0013g0258a0001c0002t0001g0082others(5): Show | 8 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284+977_1284+992d others(18): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(11): Show |
C | 40 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(37): Show | 40 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.1284+975_1284+992d others(20): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(15): Show |
C | 3 | a0001c0001t0002g0265a0001c0002t0019g0006a0001c0002t0020g0007 | 3 | HG02486.hp1 HG03579.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1284+971_1284+992d others(24): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(17): Show |
C | 4 | a0001c0001t0003g0297a0001c0001t0003g0298a0001c0002t0001g0032others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+969_1284+992d others(26): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(19): Show |
C | 74 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1284+967_1284+992d others(28): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388599
|
CATATATA others(23): Show |
C | 1 | a0001c0002t0001g0075 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1284+963_1284+992d others(32): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388599 | ||||||
| chr5:75388627
|
T | TATATATA others(14): Show |
1 | a0001c0002t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1284+964_1284+965i others(23): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388627 | ||||||
| chr5:75388638
|
A | C | 2 | a0001c0001t0008g0309a0001c0001t0014g0238 | 2 | HG01891.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1284+954T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388638 | ||||||
| chr5:75388640
|
A | C | 1 | a0001c0001t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1284+952T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388640 | ||||||
| chr5:75388649
|
A | C | 1 | a0001c0002t0001g0064 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1284+943T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388649 | ||||||
| chr5:75388701
|
T | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1284+891A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388701 | ||||||
| chr5:75388867
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+725G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75388867 | ||||||
| chr5:75389124
|
G | A | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1284+468C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75389124 | ||||||
| chr5:75389287
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+305C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75389287 | ||||||
| chr5:75389358
|
A | G | 3 | a0001c0001t0003g0288a0001c0001t0003g0289a0001c0002t0004g0008 | 3 | HG02818.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1284+234T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75389358 | ||||||
| chr5:75389391
|
T | C | 1 | a0001c0002t0001g0016 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1284+201A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 12/16 | chr5 | 75389391 | ||||||
| chr5:75389695
|
A | G | 168 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(165): Show | 168 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(165): Show |
splice_region_variant&intron_variant | LOW | c.1189-8T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75389695 | ||||||
| chr5:75389931
|
G | T | 1 | a0001c0001t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1189-244C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75389931 | ||||||
| chr5:75389971
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1189-284T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75389971 | ||||||
| chr5:75390103
|
A | G | 1 | a0001c0001t0006g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1189-416T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390103 | ||||||
| chr5:75390416
|
T | G | 2 | a0001c0001t0002g0128a0001c0001t0002g0170 | 2 | NA18992.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1189-729A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390416 | ||||||
| chr5:75390517
|
T | A | 2 | a0001c0001t0014g0237a0001c0001t0014g0238 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1189-830A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390517 | ||||||
| chr5:75390544
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-857G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390544 | ||||||
| chr5:75390693
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1189-1006G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390693 | ||||||
| chr5:75390968
|
A | G | 1 | a0001c0002t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1189-1281T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390968 | ||||||
| chr5:75390968
|
A | T | 7 | a0001c0002t0001g0101a0001c0002t0001g0105a0001c0002t0001g0107others(4): Show | 7 | HG03927.hp1 NA18962.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-1281T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390968 | ||||||
| chr5:75390974
|
T | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1189-1287A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75390974 | ||||||
| chr5:75391015
|
C | G | 40 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1189-1328G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391015 | ||||||
| chr5:75391106
|
A | C | 75 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(72): Show | 75 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1189-1419T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391106 | ||||||
| chr5:75391199
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1189-1512A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391199 | ||||||
| chr5:75391427
|
C | T | 122 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(119): Show | 122 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1189-1740G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391427 | ||||||
| chr5:75391686
|
G | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1189-1999C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391686 | ||||||
| chr5:75391716
|
C | G | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1189-2029G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391716 | ||||||
| chr5:75391764
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1189-2077A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391764 | ||||||
| chr5:75391984
|
A | G | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1189-2297T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75391984 | ||||||
| chr5:75392025
|
G | A | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1189-2338C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392025 | ||||||
| chr5:75392057
|
G | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1189-2370C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392057 | ||||||
| chr5:75392143
|
G | A | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1189-2456C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392143 | ||||||
| chr5:75392240
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1189-2553G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392240 | ||||||
| chr5:75392274
|
G | A | 1 | a0001c0001t0003g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1189-2587C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392274 | ||||||
| chr5:75392378
|
C | G | 1 | a0001c0002t0001g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1189-2691G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392378 | ||||||
| chr5:75392416
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1189-2729T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392416 | ||||||
| chr5:75392442
|
A | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0094a0001c0002t0001g0095others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2755T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392442 | ||||||
| chr5:75392740
|
C | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1189-3053G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392740 | ||||||
| chr5:75392742
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-3055C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392742 | ||||||
| chr5:75392863
|
A | G | 128 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(125): Show | 128 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1189-3176T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392863 | ||||||
| chr5:75392951
|
C | G | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0057 | 3 | HG00140.hp2 HG01106.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1189-3264G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392951 | ||||||
| chr5:75392969
|
C | CA | 31 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(28): Show | 31 | HG00735.hp1 HG01081.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.1189-3283dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392969 | ||||||
| chr5:75392969
|
C | CAA | 13 | a0001c0001t0001g0319a0001c0001t0002g0167a0001c0001t0003g0132others(10): Show | 13 | HG01358.hp2 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1189-3284_1189-328 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392969 | ||||||
| chr5:75392969
|
C | CAAA | 8 | a0001c0001t0003g0172a0001c0001t0003g0301a0001c0001t0003g0305others(5): Show | 8 | HG00642.hp1 HG01123.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1189-3285_1189-328 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392969 | ||||||
| chr5:75392969
|
CA | C | 114 | a0001c0001t0001g0036a0001c0001t0002g0127a0001c0001t0002g0136others(111): Show | 114 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.1189-3283delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392969 | ||||||
| chr5:75392969
|
CAA | C | 7 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0002t0001g0032others(4): Show | 7 | HG02486.hp1 HG02735.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-3284_1189-328 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75392969 | ||||||
| chr5:75393030
|
T | TA | 7 | a0001c0001t0002g0210a0001c0002t0009g0323a0001c0002t0009g0324others(4): Show | 7 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-3344dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393030 | ||||||
| chr5:75393066
|
C | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1189-3379G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393066 | ||||||
| chr5:75393220
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1189-3533G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393220 | ||||||
| chr5:75393414
|
T | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-3727A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393414 | ||||||
| chr5:75393416
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-3729A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393416 | ||||||
| chr5:75393424
|
T | C | 241 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(238): Show | 241 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(238): Show |
intron_variant | MODIFIER | c.1189-3737A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393424 | ||||||
| chr5:75393602
|
T | TAA | 55 | a0001c0001t0002g0127a0001c0001t0002g0136a0001c0001t0002g0138others(52): Show | 55 | HG00621.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1189-3917_1189-391 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAA | 30 | a0001c0001t0002g0265a0001c0001t0003g0120a0001c0001t0003g0293others(27): Show | 30 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1189-3919_1189-391 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAA | 28 | a0001c0002t0001g0047a0001c0002t0001g0088a0001c0002t0001g0089others(25): Show | 28 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1189-3920_1189-391 others(9): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(3): Show |
4 | a0001c0001t0002g0005a0001c0001t0003g0132a0001c0001t0010g0003others(1): Show | 4 | HG03704.hp1 NA18522.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-3925_1189-391 others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0167 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1189-3927_1189-391 others(16): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(8): Show |
2 | a0001c0001t0002g0193a0001c0001t0002g0217 | 2 | HG01516.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1189-3930_1189-391 others(19): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(9): Show |
2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1189-3931_1189-391 others(20): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(10): Show |
3 | a0001c0001t0003g0287a0001c0001t0003g0289a0001c0001t0003g0290 | 3 | HG01243.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1189-3932_1189-391 others(21): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(11): Show |
6 | a0001c0001t0003g0176a0001c0001t0003g0178a0001c0001t0003g0288others(3): Show | 6 | HG00544.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-3933_1189-391 others(22): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(12): Show |
12 | a0001c0001t0001g0310a0001c0001t0001g0318a0001c0001t0001g0320others(9): Show | 12 | HG00735.hp1 HG02622.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1189-3934_1189-391 others(23): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(13): Show |
23 | a0001c0001t0001g0311a0001c0001t0001g0313a0001c0001t0001g0316others(20): Show | 23 | HG00438.hp1 HG00597.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1189-3935_1189-391 others(24): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(14): Show |
26 | a0001c0001t0001g0314a0001c0001t0002g0214a0001c0001t0002g0221others(23): Show | 26 | HG00741.hp1 HG01257.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.1189-3936_1189-391 others(25): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(15): Show |
23 | a0001c0001t0002g0133a0001c0001t0002g0162a0001c0001t0002g0184others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(26): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(16): Show |
24 | a0001c0001t0001g0312a0001c0001t0002g0163a0001c0001t0002g0166others(21): Show | 24 | HG01071.hp2 HG01109.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(27): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(17): Show |
11 | a0001c0001t0002g0168a0001c0001t0002g0171a0001c0001t0002g0189others(8): Show | 11 | HG00621.hp1 HG01123.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(28): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(19): Show |
6 | a0001c0001t0002g0207a0001c0001t0002g0225a0001c0001t0002g0260others(3): Show | 6 | HG02300.hp2 HG02683.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(30): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(20): Show |
8 | a0001c0001t0002g0119a0001c0001t0002g0196a0001c0001t0002g0197others(5): Show | 8 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(31): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(21): Show |
5 | a0001c0001t0001g0036a0001c0001t0002g0215a0001c0001t0007g0186others(2): Show | 5 | HG00597.hp2 HG01169.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(32): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(22): Show |
5 | a0001c0001t0002g0187a0001c0001t0002g0216a0001c0001t0002g0218others(2): Show | 5 | HG01167.hp1 HG02109.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(33): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(23): Show |
3 | a0001c0001t0001g0317a0001c0001t0002g0194a0001c0001t0017g0253 | 3 | HG01257.hp1 HG02572.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(34): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(24): Show |
1 | a0001c0001t0002g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1189-3916_1189-391 others(35): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(25): Show |
4 | a0001c0001t0002g0165a0001c0001t0002g0199a0001c0001t0002g0229others(1): Show | 4 | HG02572.hp2 HG03654.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(36): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(26): Show |
1 | a0001c0001t0002g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1189-3916_1189-391 others(37): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(27): Show |
2 | a0001c0001t0002g0205a0001c0001t0007g0173 | 2 | NA18947.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(38): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(28): Show |
1 | a0001c0001t0002g0220 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1189-3916_1189-391 others(39): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(34): Show |
1 | a0001c0001t0002g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1189-3916_1189-391 others(45): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TAAAAAAA others(37): Show |
1 | a0001c0002t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1189-3916_1189-391 others(48): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TTAAAAAA others(15): Show |
1 | a0001c0001t0002g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1189-3916_1189-391 others(26): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
T | TTAAAAAA others(16): Show |
2 | a0001c0001t0002g0204a0001c0001t0002g0210 | 2 | NA19079.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1189-3916_1189-391 others(27): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
TAAA | T | 8 | a0001c0001t0003g0297a0001c0001t0003g0298a0001c0002t0001g0082others(5): Show | 8 | HG02559.hp2 HG03098.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1189-3918_1189-391 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393602
|
TAAAAAA | T | 12 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(9): Show | 12 | HG02027.hp2 NA18747.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.1189-3921_1189-391 others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393602 | ||||||
| chr5:75393623
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0219 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1189-3937_1189-393 others(16): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393623 | ||||||
| chr5:75393624
|
G | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189-3937C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393624 | ||||||
| chr5:75393657
|
C | A | 1 | a0001c0002t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1189-3970G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393657 | ||||||
| chr5:75393890
|
G | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1189-4203C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393890 | ||||||
| chr5:75393909
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-4222C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75393909 | ||||||
| chr5:75394205
|
G | C | 27 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(24): Show | 27 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.1189-4518C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394205 | ||||||
| chr5:75394251
|
T | C | 16 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(13): Show | 16 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-4564A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394251 | ||||||
| chr5:75394434
|
G | A | 1 | a0001c0001t0011g0230 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1189-4747C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394434 | ||||||
| chr5:75394479
|
A | T | 151 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(148): Show | 151 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1189-4792T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394479 | ||||||
| chr5:75394587
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+4723T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394587 | ||||||
| chr5:75394620
|
G | C | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1188+4690C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394620 | ||||||
| chr5:75394668
|
G | C | 1 | a0001c0001t0008g0261 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1188+4642C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394668 | ||||||
| chr5:75394789
|
C | T | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1188+4521G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394789 | ||||||
| chr5:75394852
|
T | C | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+4458A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75394852 | ||||||
| chr5:75395248
|
A | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+4062T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395248 | ||||||
| chr5:75395507
|
G | C | 1 | a0001c0001t0013g0258 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1188+3803C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395507 | ||||||
| chr5:75395524
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+3786A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395524 | ||||||
| chr5:75395555
|
C | CA | 105 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0135others(102): Show | 105 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1188+3754dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395555 | ||||||
| chr5:75395555
|
C | CAA | 36 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0313others(33): Show | 36 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1188+3753_1188+375 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395555 | ||||||
| chr5:75395555
|
C | CAAA | 12 | a0001c0001t0001g0312a0001c0001t0001g0317a0001c0001t0001g0322others(9): Show | 12 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1188+3752_1188+375 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395555 | ||||||
| chr5:75395555
|
CA | C | 6 | a0001c0001t0007g0224a0001c0001t0014g0237a0001c0002t0001g0099others(3): Show | 6 | HG01081.hp2 HG01516.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+3754delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395555 | ||||||
| chr5:75395555
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1188+3745_1188+375 others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395555 | ||||||
| chr5:75395580
|
T | G | 1 | a0001c0001t0002g0222 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1188+3730A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395580 | ||||||
| chr5:75395660
|
G | A | 1 | a0001c0001t0010g0003 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1188+3650C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395660 | ||||||
| chr5:75395707
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+3603G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395707 | ||||||
| chr5:75395749
|
C | A | 1 | a0001c0002t0001g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1188+3561G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395749 | ||||||
| chr5:75395765
|
G | A | 8 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+3545C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395765 | ||||||
| chr5:75395881
|
AAACAAC | A | 4 | a0001c0001t0002g0174a0001c0001t0002g0181a0001c0001t0002g0182others(1): Show | 4 | HG01192.hp1 HG01261.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+3423_1188+342 others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395881 | ||||||
| chr5:75395959
|
G | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1188+3351C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75395959 | ||||||
| chr5:75396004
|
G | A | 2 | a0001c0002t0001g0093a0001c0002t0001g0098 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1188+3306C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396004 | ||||||
| chr5:75396148
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1188+3162A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396148 | ||||||
| chr5:75396233
|
T | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+3077A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396233 | ||||||
| chr5:75396352
|
T | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1188+2958A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396352 | ||||||
| chr5:75396364
|
T | C | 1 | a0001c0001t0011g0161 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1188+2946A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396364 | ||||||
| chr5:75396464
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+2846A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396464 | ||||||
| chr5:75396498
|
G | A | 3 | a0001c0002t0001g0013a0001c0002t0001g0073a0001c0002t0001g0076 | 3 | HG02165.hp2 NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1188+2812C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396498 | ||||||
| chr5:75396501
|
C | A | 1 | a0001c0001t0002g0122 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1188+2809G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396501 | ||||||
| chr5:75396589
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+2721A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396589 | ||||||
| chr5:75396643
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1188+2667G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396643 | ||||||
| chr5:75396714
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+2596T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396714 | ||||||
| chr5:75396725
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1188+2585C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396725 | ||||||
| chr5:75396729
|
C | CA | 82 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(79): Show | 82 | HG00673.hp1 HG00735.hp1 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.1188+2580dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396729 | ||||||
| chr5:75396729
|
C | CAA | 6 | a0001c0001t0003g0292a0001c0001t0013g0243a0001c0002t0001g0085others(3): Show | 6 | HG01123.hp2 HG02630.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+2579_1188+258 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396729 | ||||||
| chr5:75396729
|
CA | C | 76 | a0001c0001t0002g0198a0001c0002t0001g0009a0001c0002t0001g0010others(73): Show | 76 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1188+2580delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396729 | ||||||
| chr5:75396739
|
A | AC | 12 | a0001c0001t0003g0172a0001c0001t0003g0242a0001c0001t0003g0244others(9): Show | 12 | HG00642.hp1 HG01192.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+2570_1188+257 others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396739 | ||||||
| chr5:75396745
|
A | C | 1 | a0001c0002t0001g0333 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1188+2565T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396745 | ||||||
| chr5:75396752
|
A | C | 1 | a0001c0001t0010g0002 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1188+2558T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396752 | ||||||
| chr5:75396764
|
G | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188+2546C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396764 | ||||||
| chr5:75396782
|
A | G | 2 | a0001c0001t0002g0121a0001c0001t0002g0125 | 2 | NA18942.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1188+2528T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396782 | ||||||
| chr5:75396921
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1188+2389T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396921 | ||||||
| chr5:75396951
|
A | G | 231 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(228): Show | 231 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.1188+2359T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396951 | ||||||
| chr5:75396985
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1188+2325A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75396985 | ||||||
| chr5:75397162
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1188+2148G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397162 | ||||||
| chr5:75397383
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1188+1927T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397383 | ||||||
| chr5:75397384
|
C | G | 1 | a0001c0002t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1188+1926G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397384 | ||||||
| chr5:75397462
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1188+1848T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397462 | ||||||
| chr5:75397474
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1188+1836C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397474 | ||||||
| chr5:75397721
|
T | G | 7 | a0001c0002t0001g0028a0001c0002t0001g0034a0001c0002t0001g0064others(4): Show | 7 | HG02040.hp2 HG02735.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188+1589A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397721 | ||||||
| chr5:75397932
|
T | C | 1 | a0001c0001t0002g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1188+1378A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75397932 | ||||||
| chr5:75398039
|
A | T | 7 | a0001c0001t0003g0132a0001c0002t0009g0323a0001c0002t0009g0324others(4): Show | 7 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1188+1271T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75398039 | ||||||
| chr5:75398087
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1188+1223T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75398087 | ||||||
| chr5:75398458
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1188+852A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75398458 | ||||||
| chr5:75398629
|
A | G | 2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1188+681T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75398629 | ||||||
| chr5:75398693
|
C | T | 9 | a0001c0001t0002g0197a0001c0001t0002g0204a0001c0001t0002g0206others(6): Show | 9 | HG00673.hp1 HG02056.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1188+617G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75398693 | ||||||
| chr5:75398872
|
T | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1188+438A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 11/16 | chr5 | 75398872 | ||||||
| chr5:75399911
|
G | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110+294C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 10/16 | chr5 | 75399911 | ||||||
| chr5:75399951
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1110+254A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 10/16 | chr5 | 75399951 | ||||||
| chr5:75399968
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+237A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 10/16 | chr5 | 75399968 | ||||||
| chr5:75399995
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+210C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 10/16 | chr5 | 75399995 | ||||||
| chr5:75400114
|
G | C | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG01256.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1110+91C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 10/16 | chr5 | 75400114 | ||||||
| chr5:75400439
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1018-142G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400439 | ||||||
| chr5:75400535
|
G | A | 1 | a0001c0001t0008g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1018-238C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400535 | ||||||
| chr5:75400543
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1018-246A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400543 | ||||||
| chr5:75400602
|
C | T | 5 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-305G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400602 | ||||||
| chr5:75400794
|
CCTTCATC others(1): Show |
C | 9 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0175others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018-505_1018-498d others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400794 | ||||||
| chr5:75400813
|
C | G | 16 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(13): Show | 16 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1018-516G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400813 | ||||||
| chr5:75400868
|
CATTT | C | 16 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(13): Show | 16 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1018-575_1018-572d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400868 | ||||||
| chr5:75400954
|
G | A | 76 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(73): Show | 76 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1018-657C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75400954 | ||||||
| chr5:75401068
|
C | A | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-771G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401068 | ||||||
| chr5:75401225
|
T | G | 60 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(57): Show | 60 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1018-928A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401225 | ||||||
| chr5:75401380
|
T | C | 5 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1083A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401380 | ||||||
| chr5:75401718
|
A | G | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+1254T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401718 | ||||||
| chr5:75401788
|
A | G | 7 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017+1184T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401788 | ||||||
| chr5:75401816
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+1156A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401816 | ||||||
| chr5:75401969
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1017+1003T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401969 | ||||||
| chr5:75401995
|
T | C | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG02559.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+977A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401995 | ||||||
| chr5:75401996
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1017+976G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75401996 | ||||||
| chr5:75402211
|
A | C | 1 | a0001c0002t0001g0025 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1017+761T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402211 | ||||||
| chr5:75402331
|
C | T | 7 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017+641G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402331 | ||||||
| chr5:75402552
|
A | G | 1 | a0001c0001t0002g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1017+420T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402552 | ||||||
| chr5:75402626
|
G | A | 5 | a0001c0002t0001g0064a0001c0002t0001g0065a0001c0002t0001g0066others(2): Show | 5 | HG02040.hp2 NA18960.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+346C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402626 | ||||||
| chr5:75402662
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+310G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402662 | ||||||
| chr5:75402670
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+302G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402670 | ||||||
| chr5:75402671
|
G | A | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1017+301C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402671 | ||||||
| chr5:75402683
|
C | T | 5 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+289G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402683 | ||||||
| chr5:75402749
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1017+223C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402749 | ||||||
| chr5:75402766
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+206A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402766 | ||||||
| chr5:75402799
|
C | CA | 7 | a0001c0001t0007g0186a0001c0001t0013g0243a0001c0001t0013g0258others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017+172dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402799 | ||||||
| chr5:75402799
|
CA | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+172delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402799 | ||||||
| chr5:75402853
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1017+119T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402853 | ||||||
| chr5:75402925
|
T | C | 1 | a0001c0001t0008g0264 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1017+47A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 9/16 | chr5 | 75402925 | ||||||
| chr5:75403218
|
G | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.931-160C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403218 | ||||||
| chr5:75403227
|
C | A | 1 | a0001c0001t0002g0213 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.931-169G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403227 | ||||||
| chr5:75403227
|
C | CAT | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-170_931-169ins others(2): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403227 | ||||||
| chr5:75403595
|
T | C | 6 | a0001c0002t0001g0028a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG02040.hp2 HG03490.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.931-537A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403595 | ||||||
| chr5:75403664
|
T | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.931-606A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403664 | ||||||
| chr5:75403735
|
T | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-677A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403735 | ||||||
| chr5:75403965
|
T | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-907A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75403965 | ||||||
| chr5:75404040
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931-982C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404040 | ||||||
| chr5:75404066
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-1008C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404066 | ||||||
| chr5:75404198
|
T | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-1140A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404198 | ||||||
| chr5:75404270
|
A | G | 28 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(25): Show | 28 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.931-1212T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404270 | ||||||
| chr5:75404273
|
C | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.931-1215G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404273 | ||||||
| chr5:75404283
|
C | G | 6 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0332others(3): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-1225G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404283 | ||||||
| chr5:75404291
|
T | TA | 25 | a0001c0001t0002g0160a0001c0001t0002g0181a0001c0001t0002g0212others(22): Show | 25 | HG00621.hp2 HG00741.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.931-1234dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404291 | ||||||
| chr5:75404291
|
T | TAAAAA | 8 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(5): Show | 8 | HG02027.hp1 HG02132.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-1238_931-1234d others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404291 | ||||||
| chr5:75404291
|
TA | T | 112 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0315others(109): Show | 112 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.931-1234delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404291 | ||||||
| chr5:75404302
|
A | C | 74 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.931-1244T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404302 | ||||||
| chr5:75404378
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.931-1320C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404378 | ||||||
| chr5:75404880
|
C | T | 1 | a0001c0002t0001g0078 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.931-1822G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404880 | ||||||
| chr5:75404972
|
C | T | 31 | a0001c0001t0002g0127a0001c0001t0002g0135a0001c0001t0002g0136others(28): Show | 31 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.931-1914G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404972 | ||||||
| chr5:75404994
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-1936A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75404994 | ||||||
| chr5:75405016
|
A | AAAC | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.931-1961_931-1959d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405016 | ||||||
| chr5:75405145
|
T | A | 1 | a0001c0002t0001g0064 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.931-2087A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405145 | ||||||
| chr5:75405307
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.931-2249A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405307 | ||||||
| chr5:75405638
|
T | C | 81 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.931-2580A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405638 | ||||||
| chr5:75405659
|
T | C | 1 | a0001c0001t0008g0266 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-2601A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405659 | ||||||
| chr5:75405800
|
TACATATA others(14): Show |
T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.931-2763_931-2743d others(23): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405800 | ||||||
| chr5:75405837
|
C | G | 79 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(76): Show | 79 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.931-2779G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405837 | ||||||
| chr5:75405872
|
TG | T | 124 | a0001c0001t0001g0036a0001c0001t0002g0119a0001c0001t0002g0121others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.931-2815delC | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405872 | ||||||
| chr5:75405872
|
TGG | T | 140 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(137): Show | 140 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.931-2816_931-2815d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405872 | ||||||
| chr5:75405875
|
G | T | 3 | a0001c0001t0010g0001a0001c0002t0019g0006a0001c0002t0020g0007 | 3 | HG02071.hp1 HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.931-2817C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405875 | ||||||
| chr5:75405880
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.931-2822C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405880 | ||||||
| chr5:75405941
|
T | C | 27 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0002t0001g0068others(24): Show | 27 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.931-2883A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75405941 | ||||||
| chr5:75406006
|
T | C | 3 | a0001c0001t0012g0240a0001c0001t0012g0241a0001c0002t0001g0248 | 3 | HG02723.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.931-2948A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406006 | ||||||
| chr5:75406130
|
T | C | 2 | a0001c0001t0011g0158a0001c0001t0011g0161 | 2 | NA18968.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.931-3072A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406130 | ||||||
| chr5:75406239
|
C | G | 8 | a0001c0001t0002g0127a0001c0001t0002g0136a0001c0001t0002g0143others(5): Show | 8 | NA18948.hp1 NA18953.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.931-3181G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406239 | ||||||
| chr5:75406407
|
C | G | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-3349G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406407 | ||||||
| chr5:75406542
|
CT | C | 6 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0155others(3): Show | 6 | HG01256.hp1 NA18953.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-3485delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406542 | ||||||
| chr5:75406681
|
A | T | 1 | a0001c0001t0006g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931-3623T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406681 | ||||||
| chr5:75406682
|
G | C | 1 | a0001c0001t0006g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931-3624C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406682 | ||||||
| chr5:75406684
|
T | G | 1 | a0001c0001t0006g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931-3626A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406684 | ||||||
| chr5:75406902
|
C | A | 2 | a0001c0001t0012g0240a0001c0001t0012g0241 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.931-3844G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406902 | ||||||
| chr5:75406904
|
G | C | 1 | a0001c0001t0002g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.931-3846C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406904 | ||||||
| chr5:75406912
|
A | C | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG01255.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.931-3854T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406912 | ||||||
| chr5:75406914
|
A | G | 1 | a0001c0001t0003g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.931-3856T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406914 | ||||||
| chr5:75406994
|
TAAAA | T | 12 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.931-3940_931-3937d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406994 | ||||||
| chr5:75406999
|
C | G | 12 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.931-3941G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75406999 | ||||||
| chr5:75407000
|
C | T | 12 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.931-3942G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407000 | ||||||
| chr5:75407068
|
A | C | 35 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(32): Show | 35 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.930+3943T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407068 | ||||||
| chr5:75407102
|
T | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.930+3909A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407102 | ||||||
| chr5:75407313
|
T | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+3698A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407313 | ||||||
| chr5:75407345
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+3666G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407345 | ||||||
| chr5:75407470
|
A | C | 2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.930+3541T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407470 | ||||||
| chr5:75407472
|
T | TA | 6 | a0001c0002t0001g0064a0001c0002t0001g0065a0001c0002t0001g0066others(3): Show | 6 | HG02040.hp2 HG03486.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+3538dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407472 | ||||||
| chr5:75407472
|
TA | T | 10 | a0001c0001t0002g0148a0001c0001t0002g0194a0001c0001t0003g0293others(7): Show | 10 | HG01257.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.930+3538delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407472 | ||||||
| chr5:75407473
|
A | T | 2 | a0001c0002t0001g0081a0001c0002t0009g0327 | 2 | HG02135.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.930+3538T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407473 | ||||||
| chr5:75407490
|
A | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.930+3521T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407490 | ||||||
| chr5:75407516
|
G | A | 31 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.930+3495C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407516 | ||||||
| chr5:75407528
|
CCAAA | C | 7 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+3479_930+3482d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407528 | ||||||
| chr5:75407615
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+3396T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407615 | ||||||
| chr5:75407743
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+3268T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407743 | ||||||
| chr5:75407856
|
C | CT | 23 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(20): Show | 23 | HG00735.hp1 HG01109.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.930+3154dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407856 | ||||||
| chr5:75407856
|
CT | C | 46 | a0001c0001t0002g0194a0001c0001t0003g0287a0001c0001t0003g0288others(43): Show | 46 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.930+3154delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407856 | ||||||
| chr5:75407900
|
T | TA | 7 | a0001c0001t0002g0217a0001c0002t0009g0323a0001c0002t0009g0324others(4): Show | 7 | HG01516.hp1 HG02027.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+3110dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407900 | ||||||
| chr5:75407900
|
TA | T | 18 | a0001c0001t0002g0211a0001c0001t0003g0172a0001c0001t0003g0192others(15): Show | 18 | HG00642.hp1 HG01192.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+3110delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75407900 | ||||||
| chr5:75408087
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+2924C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408087 | ||||||
| chr5:75408225
|
G | A | 1 | a0001c0002t0009g0323 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.930+2786C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408225 | ||||||
| chr5:75408237
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0041 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.930+2774C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408237 | ||||||
| chr5:75408307
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.930+2704A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408307 | ||||||
| chr5:75408441
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.930+2570A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408441 | ||||||
| chr5:75408443
|
C | T | 1 | a0001c0001t0002g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.930+2568G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408443 | ||||||
| chr5:75408444
|
T | A | 1 | a0001c0001t0002g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.930+2567A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408444 | ||||||
| chr5:75408444
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.930+2567A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408444 | ||||||
| chr5:75408464
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+2547G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408464 | ||||||
| chr5:75408484
|
T | C | 1 | a0001c0002t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.930+2527A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408484 | ||||||
| chr5:75408493
|
G | A | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+2518C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408493 | ||||||
| chr5:75408633
|
T | A | 1 | a0001c0001t0013g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.930+2378A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408633 | ||||||
| chr5:75408781
|
TA | T | 7 | a0001c0002t0001g0101a0001c0002t0009g0323a0001c0002t0009g0324others(4): Show | 7 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+2229delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408781 | ||||||
| chr5:75408782
|
A | T | 2 | a0001c0001t0002g0225a0001c0001t0002g0227 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.930+2229T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408782 | ||||||
| chr5:75408799
|
G | A | 6 | a0001c0002t0001g0028a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG02040.hp2 HG03490.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+2212C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408799 | ||||||
| chr5:75408876
|
G | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.930+2135C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408876 | ||||||
| chr5:75408939
|
A | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.930+2072T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75408939 | ||||||
| chr5:75409004
|
T | C | 77 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(74): Show | 77 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.930+2007A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409004 | ||||||
| chr5:75409016
|
T | C | 1 | a0001c0002t0018g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.930+1995A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409016 | ||||||
| chr5:75409219
|
CTCA | C | 11 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(8): Show | 11 | HG02027.hp2 NA18942.hp1 NA18974.hp2 others(8): Show |
intron_variant | MODIFIER | c.930+1789_930+1791d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409219 | ||||||
| chr5:75409300
|
TATTACA | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+1705_930+1710d others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409300 | ||||||
| chr5:75409378
|
G | C | 1 | a0001c0001t0005g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.930+1633C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409378 | ||||||
| chr5:75409452
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.930+1559G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409452 | ||||||
| chr5:75409489
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+1522G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409489 | ||||||
| chr5:75409513
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.930+1498G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409513 | ||||||
| chr5:75409534
|
C | CT | 33 | a0001c0002t0001g0056a0001c0002t0001g0088a0001c0002t0001g0089others(30): Show | 33 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.930+1476dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409534 | ||||||
| chr5:75409534
|
CT | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+1476delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409534 | ||||||
| chr5:75409811
|
A | G | 176 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(173): Show | 176 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.930+1200T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409811 | ||||||
| chr5:75409831
|
G | GT | 19 | a0001c0001t0001g0315a0001c0001t0002g0145a0001c0001t0002g0211others(16): Show | 19 | HG01891.hp1 HG01934.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+1179dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409831 | ||||||
| chr5:75409831
|
G | GTT | 33 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(30): Show | 33 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.930+1178_930+1179d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409831 | ||||||
| chr5:75409855
|
C | G | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.930+1156G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409855 | ||||||
| chr5:75409903
|
G | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.930+1108C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409903 | ||||||
| chr5:75409932
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+1079G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75409932 | ||||||
| chr5:75410145
|
C | T | 5 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0094others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.930+866G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410145 | ||||||
| chr5:75410147
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.930+864A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410147 | ||||||
| chr5:75410222
|
C | A | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+789G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410222 | ||||||
| chr5:75410293
|
G | T | 1 | a0001c0001t0005g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.930+718C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410293 | ||||||
| chr5:75410345
|
C | A | 1 | a0001c0002t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.930+666G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410345 | ||||||
| chr5:75410405
|
C | T | 16 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(13): Show | 16 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.930+606G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410405 | ||||||
| chr5:75410406
|
G | A | 1 | a0001c0002t0018g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.930+605C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410406 | ||||||
| chr5:75410460
|
A | T | 1 | a0001c0002t0004g0043 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.930+551T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410460 | ||||||
| chr5:75410518
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.930+493C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410518 | ||||||
| chr5:75410609
|
C | CA | 325 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.930+401dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410609 | ||||||
| chr5:75410609
|
C | CAAAAAAA others(5): Show |
5 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(2): Show | 5 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+390_930+401dup others(12): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410609 | ||||||
| chr5:75410609
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0009g0327 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.930+389_930+401dup others(13): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410609 | ||||||
| chr5:75410703
|
T | TA | 38 | a0001c0001t0002g0252a0001c0001t0003g0293a0001c0001t0003g0294others(35): Show | 38 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.930+307dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410703 | ||||||
| chr5:75410703
|
TA | T | 31 | a0001c0001t0002g0005a0001c0001t0002g0140a0001c0001t0002g0162others(28): Show | 31 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.930+307delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410703 | ||||||
| chr5:75410723
|
A | G | 2 | a0001c0001t0003g0301a0001c0001t0003g0303 | 2 | HG00642.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.930+288T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410723 | ||||||
| chr5:75410742
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.930+269A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410742 | ||||||
| chr5:75410836
|
T | C | 82 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(79): Show | 82 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.930+175A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410836 | ||||||
| chr5:75410973
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+38A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 8/16 | chr5 | 75410973 | ||||||
| chr5:75411303
|
T | G | 1 | a0001c0002t0001g0033 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.838-200A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411303 | ||||||
| chr5:75411303
|
T | TTATG | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.838-204_838-201dup others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411303 | ||||||
| chr5:75411447
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-344C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411447 | ||||||
| chr5:75411542
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-439G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411542 | ||||||
| chr5:75411936
|
C | T | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-833G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411936 | ||||||
| chr5:75411937
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.838-834C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411937 | ||||||
| chr5:75411970
|
TCTC | T | 16 | a0001c0001t0003g0132a0001c0001t0003g0172a0001c0001t0003g0192others(13): Show | 16 | HG00642.hp1 HG01192.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.838-870_838-868del others(3): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411970 | ||||||
| chr5:75411972
|
T | G | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.838-869A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75411972 | ||||||
| chr5:75412310
|
G | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-1207C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412310 | ||||||
| chr5:75412374
|
C | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.838-1271G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412374 | ||||||
| chr5:75412414
|
C | G | 5 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-1311G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412414 | ||||||
| chr5:75412648
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.838-1545T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412648 | ||||||
| chr5:75412688
|
G | C | 75 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(72): Show | 75 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.838-1585C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412688 | ||||||
| chr5:75412694
|
A | G | 2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.838-1591T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412694 | ||||||
| chr5:75412799
|
T | C | 1 | a0001c0002t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.838-1696A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412799 | ||||||
| chr5:75412804
|
G | C | 165 | a0001c0001t0003g0120a0001c0001t0003g0172a0001c0001t0003g0192others(162): Show | 165 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.838-1701C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412804 | ||||||
| chr5:75412925
|
A | G | 2 | a0001c0002t0001g0048a0001c0002t0022g0014 | 2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.838-1822T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412925 | ||||||
| chr5:75412952
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.838-1849A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75412952 | ||||||
| chr5:75413257
|
G | C | 1 | a0001c0001t0002g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.838-2154C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413257 | ||||||
| chr5:75413269
|
T | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.838-2166A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413269 | ||||||
| chr5:75413284
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-2181T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413284 | ||||||
| chr5:75413319
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.838-2216T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413319 | ||||||
| chr5:75413347
|
G | C | 1 | a0001c0001t0001g0310 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.838-2244C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413347 | ||||||
| chr5:75413486
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.838-2383C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413486 | ||||||
| chr5:75413509
|
T | C | 31 | a0001c0001t0002g0127a0001c0001t0002g0135a0001c0001t0002g0136others(28): Show | 31 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.838-2406A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413509 | ||||||
| chr5:75413568
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-2465A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413568 | ||||||
| chr5:75413668
|
T | TAC | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.838-2567_838-2566d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413668 | ||||||
| chr5:75413812
|
T | C | 5 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0141others(2): Show | 5 | HG01934.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-2709A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75413812 | ||||||
| chr5:75414114
|
CA | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+2761delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414114 | ||||||
| chr5:75414315
|
C | T | 3 | a0001c0001t0002g0204a0001c0001t0002g0208a0001c0001t0002g0210 | 3 | HG02056.hp2 NA19079.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.837+2561G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414315 | ||||||
| chr5:75414346
|
T | TA | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+2529dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414346 | ||||||
| chr5:75414432
|
G | A | 10 | a0001c0001t0002g0185a0001c0001t0002g0193a0001c0001t0002g0225others(7): Show | 10 | HG00735.hp2 HG02165.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+2444C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414432 | ||||||
| chr5:75414448
|
A | T | 1 | a0001c0001t0002g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.837+2428T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414448 | ||||||
| chr5:75414555
|
C | CTA | 12 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(9): Show | 12 | HG00621.hp2 HG00673.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+2320_837+2321i others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414555 | ||||||
| chr5:75414725
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.837+2151C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414725 | ||||||
| chr5:75414999
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+1877G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75414999 | ||||||
| chr5:75415035
|
T | C | 1 | a0001c0002t0001g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.837+1841A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415035 | ||||||
| chr5:75415035
|
T | TAC | 4 | a0001c0001t0002g0183a0001c0001t0007g0224a0001c0002t0001g0091others(1): Show | 4 | HG01071.hp2 HG02165.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+1839_837+1840d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415035 | ||||||
| chr5:75415037
|
C | T | 7 | a0001c0001t0003g0305a0001c0001t0003g0306a0001c0002t0009g0324others(4): Show | 7 | HG02027.hp1 HG02132.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.837+1839G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415037 | ||||||
| chr5:75415079
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.837+1797T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415079 | ||||||
| chr5:75415467
|
G | A | 1 | a0001c0001t0012g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.837+1409C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415467 | ||||||
| chr5:75415489
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+1387G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415489 | ||||||
| chr5:75415534
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.837+1342G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415534 | ||||||
| chr5:75415904
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.837+972A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75415904 | ||||||
| chr5:75416052
|
A | C | 1 | a0001c0001t0002g0222 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.837+824T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75416052 | ||||||
| chr5:75416529
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+347T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75416529 | ||||||
| chr5:75416775
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.837+101T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 7/16 | chr5 | 75416775 | ||||||
| chr5:75417186
|
C | T | 2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.680-153G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417186 | ||||||
| chr5:75417233
|
A | G | 2 | a0001c0001t0005g0275a0001c0001t0005g0276 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.680-200T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417233 | ||||||
| chr5:75417587
|
T | G | 41 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.680-554A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417587 | ||||||
| chr5:75417631
|
T | C | 2 | a0001c0001t0006g0233a0001c0006t0006g0268 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.680-598A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417631 | ||||||
| chr5:75417655
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680-622G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417655 | ||||||
| chr5:75417808
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.680-775A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417808 | ||||||
| chr5:75417843
|
A | T | 2 | a0001c0001t0012g0240a0001c0001t0012g0241 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.680-810T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417843 | ||||||
| chr5:75417868
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.680-835T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417868 | ||||||
| chr5:75417917
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.680-884C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417917 | ||||||
| chr5:75417931
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.680-898G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75417931 | ||||||
| chr5:75418053
|
G | C | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.680-1020C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418053 | ||||||
| chr5:75418127
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.680-1094C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418127 | ||||||
| chr5:75418579
|
C | T | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.679+762G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418579 | ||||||
| chr5:75418621
|
T | A | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+720A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418621 | ||||||
| chr5:75418645
|
T | C | 1 | a0001c0002t0001g0016 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.679+696A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418645 | ||||||
| chr5:75418649
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+692C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418649 | ||||||
| chr5:75418878
|
G | A | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.679+463C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418878 | ||||||
| chr5:75418959
|
G | A | 40 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.679+382C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75418959 | ||||||
| chr5:75419036
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.679+305T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75419036 | ||||||
| chr5:75419269
|
A | C | 1 | a0001c0002t0001g0048 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.679+72T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 6/16 | chr5 | 75419269 | ||||||
| chr5:75419668
|
C | T | 9 | a0001c0001t0003g0172a0001c0001t0003g0299a0001c0001t0003g0300others(6): Show | 9 | HG00642.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.596-244G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75419668 | ||||||
| chr5:75419800
|
ACT | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-378_596-377del others(2): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75419800 | ||||||
| chr5:75419895
|
C | A | 1 | a0001c0002t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596-471G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75419895 | ||||||
| chr5:75419916
|
T | C | 1 | a0001c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.596-492A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75419916 | ||||||
| chr5:75420124
|
G | T | 1 | a0001c0002t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.596-700C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420124 | ||||||
| chr5:75420178
|
T | C | 47 | a0001c0001t0002g0127a0001c0001t0002g0135a0001c0001t0002g0136others(44): Show | 47 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.596-754A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420178 | ||||||
| chr5:75420239
|
A | G | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.596-815T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420239 | ||||||
| chr5:75420281
|
A | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-857T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420281 | ||||||
| chr5:75420347
|
G | GT | 16 | a0001c0001t0002g0123a0001c0001t0002g0144a0001c0001t0002g0265others(13): Show | 16 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.596-924dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420347 | ||||||
| chr5:75420347
|
GT | G | 80 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0002t0001g0009others(77): Show | 80 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.596-924delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420347 | ||||||
| chr5:75420365
|
G | A | 9 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(6): Show | 9 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.596-941C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420365 | ||||||
| chr5:75420562
|
G | A | 1 | a0001c0002t0001g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.596-1138C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420562 | ||||||
| chr5:75420718
|
G | A | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-1294C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420718 | ||||||
| chr5:75420722
|
CAT | C | 3 | a0001c0001t0006g0134a0001c0001t0006g0256a0001c0001t0006g0308 | 3 | HG02615.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.596-1300_596-1299d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420722 | ||||||
| chr5:75420868
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-1444G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420868 | ||||||
| chr5:75420872
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-1448C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420872 | ||||||
| chr5:75420935
|
C | A | 1 | a0001c0002t0001g0013 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596-1511G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420935 | ||||||
| chr5:75420962
|
G | A | 7 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0126others(4): Show | 7 | NA18942.hp1 NA18981.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.596-1538C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420962 | ||||||
| chr5:75420980
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.596-1556C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75420980 | ||||||
| chr5:75421034
|
C | CCTGAGCT others(8): Show |
1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.596-1625_596-1611d others(17): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421034 | ||||||
| chr5:75421131
|
A | G | 8 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 8 | HG00735.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.596-1707T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421131 | ||||||
| chr5:75421138
|
C | G | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.596-1714G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421138 | ||||||
| chr5:75421231
|
A | G | 1 | a0001c0002t0001g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.596-1807T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421231 | ||||||
| chr5:75421277
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.596-1853G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421277 | ||||||
| chr5:75421378
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-1954G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421378 | ||||||
| chr5:75421828
|
C | T | 126 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(123): Show | 126 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.596-2404G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421828 | ||||||
| chr5:75421936
|
C | T | 4 | a0001c0001t0002g0188a0001c0001t0002g0202a0001c0001t0002g0249others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-2512G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421936 | ||||||
| chr5:75421942
|
G | A | 186 | a0001c0001t0003g0120a0001c0001t0003g0131a0001c0001t0003g0132others(183): Show | 186 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.596-2518C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421942 | ||||||
| chr5:75421986
|
T | A | 68 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(65): Show | 68 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.596-2562A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75421986 | ||||||
| chr5:75422041
|
A | G | 1 | a0001c0001t0007g0224 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.596-2617T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75422041 | ||||||
| chr5:75422296
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-2872G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75422296 | ||||||
| chr5:75422347
|
G | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.596-2923C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75422347 | ||||||
| chr5:75422623
|
AAATCAAA others(5): Show |
A | 6 | a0001c0002t0001g0031a0001c0002t0001g0049a0001c0002t0001g0050others(3): Show | 6 | HG00741.hp1 HG02004.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.595+2726_595+2737d others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75422623 | ||||||
| chr5:75422794
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.595+2567A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75422794 | ||||||
| chr5:75422808
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+2553A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75422808 | ||||||
| chr5:75423204
|
C | T | 1 | a0001c0001t0005g0274 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595+2157G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423204 | ||||||
| chr5:75423226
|
T | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.595+2135A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423226 | ||||||
| chr5:75423349
|
A | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.595+2012T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423349 | ||||||
| chr5:75423384
|
GA | G | 158 | a0001c0001t0001g0318a0001c0001t0002g0005a0001c0001t0002g0125others(155): Show | 158 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.595+1976delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423384 | ||||||
| chr5:75423384
|
GAA | G | 17 | a0001c0001t0003g0120a0001c0001t0003g0192a0001c0001t0003g0287others(14): Show | 17 | HG00597.hp1 HG01081.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.595+1975_595+1976d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423384 | ||||||
| chr5:75423385
|
A | G | 1 | a0001c0001t0008g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.595+1976T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423385 | ||||||
| chr5:75423504
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.595+1857A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423504 | ||||||
| chr5:75423518
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.595+1843A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423518 | ||||||
| chr5:75423660
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.595+1701C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75423660 | ||||||
| chr5:75424227
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+1134G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424227 | ||||||
| chr5:75424296
|
A | G | 1 | a0001c0002t0001g0021 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.595+1065T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424296 | ||||||
| chr5:75424309
|
C | T | 1 | a0001c0001t0002g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.595+1052G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424309 | ||||||
| chr5:75424415
|
T | C | 1 | a0001c0001t0002g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.595+946A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424415 | ||||||
| chr5:75424503
|
C | T | 3 | a0001c0001t0003g0293a0001c0002t0019g0006a0001c0002t0020g0007 | 3 | HG02055.hp1 HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.595+858G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424503 | ||||||
| chr5:75424520
|
C | T | 2 | a0001c0002t0001g0027a0001c0002t0001g0035 | 2 | HG03490.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.595+841G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424520 | ||||||
| chr5:75424618
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+743T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424618 | ||||||
| chr5:75424786
|
A | G | 2 | a0001c0001t0002g0196a0001c0001t0002g0207 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.595+575T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424786 | ||||||
| chr5:75424838
|
T | C | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.595+523A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424838 | ||||||
| chr5:75424864
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+497T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424864 | ||||||
| chr5:75424867
|
C | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.595+494G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75424867 | ||||||
| chr5:75425008
|
C | A | 4 | a0001c0002t0001g0089a0001c0002t0001g0094a0001c0002t0001g0095others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+353G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75425008 | ||||||
| chr5:75425045
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+316T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75425045 | ||||||
| chr5:75425072
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.595+289G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75425072 | ||||||
| chr5:75425083
|
A | G | 1 | a0001c0002t0001g0072 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.595+278T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 5/16 | chr5 | 75425083 | ||||||
| chr5:75425562
|
T | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.457-63A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75425562 | ||||||
| chr5:75425618
|
G | A | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-119C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75425618 | ||||||
| chr5:75425635
|
A | G | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-136T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75425635 | ||||||
| chr5:75425803
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-304C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75425803 | ||||||
| chr5:75426078
|
T | A | 25 | a0001c0001t0003g0131a0001c0001t0003g0172a0001c0001t0003g0175others(22): Show | 25 | HG00642.hp1 HG01192.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.456+293A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75426078 | ||||||
| chr5:75426353
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.456+18G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75426353 | ||||||
| chr5:75426358
|
A | G | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.456+13T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 4/16 | chr5 | 75426358 | ||||||
| chr5:75426602
|
T | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-124A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75426602 | ||||||
| chr5:75426730
|
T | C | 1 | a0001c0001t0003g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.349-252A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75426730 | ||||||
| chr5:75426749
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.349-271T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75426749 | ||||||
| chr5:75427041
|
T | C | 2 | a0001c0001t0013g0243a0001c0001t0013g0258 | 2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.349-563A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427041 | ||||||
| chr5:75427053
|
A | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-575T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427053 | ||||||
| chr5:75427393
|
G | A | 1 | a0001c0002t0004g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.349-915C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427393 | ||||||
| chr5:75427484
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.349-1006C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427484 | ||||||
| chr5:75427596
|
CA | C | 40 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.349-1119delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427596 | ||||||
| chr5:75427693
|
T | G | 1 | a0001c0001t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349-1215A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427693 | ||||||
| chr5:75427809
|
T | C | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1331A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75427809 | ||||||
| chr5:75428095
|
T | C | 2 | a0001c0001t0002g0225a0001c0001t0002g0227 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.349-1617A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428095 | ||||||
| chr5:75428313
|
A | AAACT | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-1836_349-1835i others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428313 | ||||||
| chr5:75428315
|
AC | A | 75 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(72): Show | 75 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.349-1838delG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428315 | ||||||
| chr5:75428360
|
G | A | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-1882C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428360 | ||||||
| chr5:75428402
|
G | T | 75 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(72): Show | 75 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.349-1924C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428402 | ||||||
| chr5:75428416
|
C | T | 8 | a0001c0002t0001g0078a0001c0002t0001g0329a0001c0002t0001g0330others(5): Show | 8 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-1938G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428416 | ||||||
| chr5:75428494
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0252a0001c0001t0017g0253 | 3 | HG01069.hp2 HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.349-2016G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428494 | ||||||
| chr5:75428520
|
T | C | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-2042A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428520 | ||||||
| chr5:75428533
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-2055G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428533 | ||||||
| chr5:75428545
|
G | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-2067C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428545 | ||||||
| chr5:75428551
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-2073C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428551 | ||||||
| chr5:75428564
|
G | C | 13 | a0001c0002t0001g0030a0001c0002t0001g0038a0001c0002t0001g0042others(10): Show | 13 | HG00597.hp1 HG02523.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-2086C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428564 | ||||||
| chr5:75428602
|
T | C | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-2124A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428602 | ||||||
| chr5:75428677
|
C | CA | 13 | a0001c0001t0002g0200a0001c0001t0002g0221a0001c0001t0002g0260others(10): Show | 13 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-2200dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428677 | ||||||
| chr5:75428677
|
C | CAA | 7 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-2201_349-2200d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428677 | ||||||
| chr5:75428677
|
CA | C | 8 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(5): Show | 8 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-2200delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428677 | ||||||
| chr5:75428677
|
CAA | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-2201_349-2200d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428677 | ||||||
| chr5:75428775
|
CTGT | C | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-2300_349-2298d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428775 | ||||||
| chr5:75428815
|
A | G | 40 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.349-2337T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428815 | ||||||
| chr5:75428862
|
C | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-2384G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75428862 | ||||||
| chr5:75429007
|
A | C | 80 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(77): Show | 80 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.349-2529T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429007 | ||||||
| chr5:75429057
|
C | T | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-2579G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429057 | ||||||
| chr5:75429175
|
G | GAAT | 106 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(103): Show | 106 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.349-2700_349-2698d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429175 | ||||||
| chr5:75429197
|
A | AATT | 21 | a0001c0001t0001g0310a0001c0001t0003g0246a0001c0002t0001g0091others(18): Show | 21 | HG01123.hp2 HG01261.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-2722_349-2720d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429197 | ||||||
| chr5:75429197
|
A | T | 26 | a0001c0001t0002g0126a0001c0001t0002g0130a0001c0001t0002g0189others(23): Show | 26 | HG00597.hp2 HG00621.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.349-2719T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429197 | ||||||
| chr5:75429200
|
T | A | 113 | a0001c0001t0001g0317a0001c0001t0001g0321a0001c0001t0002g0127others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.349-2722A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429200 | ||||||
| chr5:75429203
|
T | A | 6 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-2725A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429203 | ||||||
| chr5:75429391
|
G | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0057 | 3 | HG00140.hp2 HG01106.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.349-2913C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429391 | ||||||
| chr5:75429454
|
C | T | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-2976G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429454 | ||||||
| chr5:75429579
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-3101C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429579 | ||||||
| chr5:75429705
|
C | A | 4 | a0001c0002t0001g0009a0001c0002t0001g0040a0001c0002t0001g0062others(1): Show | 4 | HG01943.hp2 HG02148.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-3227G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429705 | ||||||
| chr5:75429784
|
T | C | 121 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0011others(118): Show | 121 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.349-3306A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429784 | ||||||
| chr5:75429811
|
C | T | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-3333G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429811 | ||||||
| chr5:75429843
|
G | GA | 38 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0135others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.349-3366dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429843 | ||||||
| chr5:75429843
|
GA | G | 159 | a0001c0001t0003g0120a0001c0001t0003g0131a0001c0001t0003g0172others(156): Show | 159 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.349-3366delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429843 | ||||||
| chr5:75429962
|
A | G | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-3484T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75429962 | ||||||
| chr5:75430016
|
G | T | 2 | a0001c0001t0003g0242a0001c0001t0003g0246 | 2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.349-3538C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430016 | ||||||
| chr5:75430036
|
AG | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-3559delC | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430036 | ||||||
| chr5:75430037
|
G | A | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-3559C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430037 | ||||||
| chr5:75430122
|
T | C | 1 | a0001c0001t0002g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349-3644A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430122 | ||||||
| chr5:75430312
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0076 | 2 | NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.349-3834C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430312 | ||||||
| chr5:75430351
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-3873A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430351 | ||||||
| chr5:75430387
|
C | T | 1 | a0001c0001t0003g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349-3909G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430387 | ||||||
| chr5:75430486
|
C | G | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.349-4008G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430486 | ||||||
| chr5:75430564
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-4086C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430564 | ||||||
| chr5:75430646
|
C | T | 5 | a0001c0001t0006g0134a0001c0001t0006g0256a0001c0001t0006g0308others(2): Show | 5 | HG01081.hp2 HG01891.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-4168G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430646 | ||||||
| chr5:75430650
|
T | A | 3 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0277 | 3 | HG01167.hp2 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.349-4172A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430650 | ||||||
| chr5:75430738
|
A | C | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.349-4260T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430738 | ||||||
| chr5:75430790
|
C | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.349-4312G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430790 | ||||||
| chr5:75430942
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-4464C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430942 | ||||||
| chr5:75430988
|
C | CT | 14 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(11): Show | 14 | HG02027.hp2 NA18747.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-4511dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75430988 | ||||||
| chr5:75431688
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.349-5210A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75431688 | ||||||
| chr5:75431696
|
T | G | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.349-5218A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75431696 | ||||||
| chr5:75431722
|
C | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0041 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.349-5244G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75431722 | ||||||
| chr5:75432055
|
C | A | 1 | a0001c0001t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349-5577G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432055 | ||||||
| chr5:75432056
|
C | A | 1 | a0001c0001t0002g0205 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349-5578G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432056 | ||||||
| chr5:75432057
|
C | CT | 6 | a0001c0002t0001g0080a0001c0002t0001g0082a0001c0002t0001g0083others(3): Show | 6 | HG02559.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5580dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432057 | ||||||
| chr5:75432057
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.349-5579G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432057 | ||||||
| chr5:75432058
|
T | C | 27 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0172others(24): Show | 27 | HG00642.hp1 HG01192.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.349-5580A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432058 | ||||||
| chr5:75432194
|
G | A | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5716C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432194 | ||||||
| chr5:75432196
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5718G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432196 | ||||||
| chr5:75432391
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5913A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432391 | ||||||
| chr5:75432543
|
T | A | 2 | a0001c0002t0001g0093a0001c0002t0001g0098 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.349-6065A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432543 | ||||||
| chr5:75432611
|
T | G | 1 | a0001c0001t0002g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.349-6133A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432611 | ||||||
| chr5:75432744
|
T | C | 2 | a0001c0002t0001g0032a0001c0002t0001g0041 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.349-6266A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432744 | ||||||
| chr5:75432806
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-6328G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432806 | ||||||
| chr5:75432844
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-6366C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432844 | ||||||
| chr5:75432903
|
ATCT | A | 3 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0057 | 3 | HG00140.hp2 HG01106.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.349-6428_349-6426d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75432903 | ||||||
| chr5:75433059
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.349-6581A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433059 | ||||||
| chr5:75433088
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.349-6610A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433088 | ||||||
| chr5:75433096
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-6618A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433096 | ||||||
| chr5:75433396
|
G | C | 8 | a0001c0001t0002g0265a0001c0001t0008g0261a0001c0001t0008g0262others(5): Show | 8 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-6918C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433396 | ||||||
| chr5:75433448
|
T | C | 7 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-6970A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433448 | ||||||
| chr5:75433692
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.349-7214A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433692 | ||||||
| chr5:75433784
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-7306C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433784 | ||||||
| chr5:75433994
|
C | T | 6 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0277others(3): Show | 6 | HG01167.hp2 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-7516G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75433994 | ||||||
| chr5:75434039
|
T | C | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.349-7561A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434039 | ||||||
| chr5:75434068
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.349-7590A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434068 | ||||||
| chr5:75434186
|
G | GT | 94 | a0001c0001t0001g0036a0001c0001t0001g0312a0001c0001t0002g0119others(91): Show | 94 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.349-7709dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434186 | ||||||
| chr5:75434186
|
G | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.349-7708C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434186 | ||||||
| chr5:75434186
|
GT | G | 11 | a0001c0001t0002g0144a0001c0001t0002g0164a0001c0001t0002g0188others(8): Show | 11 | HG00140.hp1 HG01361.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-7709delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434186 | ||||||
| chr5:75434186
|
GTT | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-7710_349-7709d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434186 | ||||||
| chr5:75434375
|
C | T | 12 | a0001c0001t0006g0134a0001c0001t0006g0233a0001c0001t0006g0234others(9): Show | 12 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-7897G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434375 | ||||||
| chr5:75434481
|
T | C | 1 | a0001c0002t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.349-8003A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434481 | ||||||
| chr5:75434486
|
G | A | 5 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0021others(2): Show | 5 | HG02015.hp2 NA18612.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-8008C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434486 | ||||||
| chr5:75434517
|
G | GGA | 3 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0003 | 3 | HG02004.hp1 HG02071.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.349-8041_349-8040d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434517 | ||||||
| chr5:75434543
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.349-8065C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434543 | ||||||
| chr5:75434551
|
T | A | 27 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(24): Show | 27 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.349-8073A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434551 | ||||||
| chr5:75434615
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.349-8137C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434615 | ||||||
| chr5:75434640
|
G | GT | 11 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-8163dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434640 | ||||||
| chr5:75434765
|
T | C | 6 | a0001c0001t0002g0119a0001c0002t0001g0013a0001c0002t0001g0073others(3): Show | 6 | HG02165.hp2 NA18964.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-8287A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434765 | ||||||
| chr5:75434812
|
A | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | NA18953.hp1 NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.349-8334T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434812 | ||||||
| chr5:75434859
|
G | A | 1 | a0001c0001t0002g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.349-8381C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434859 | ||||||
| chr5:75434903
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.349-8425A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434903 | ||||||
| chr5:75434995
|
A | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-8517T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75434995 | ||||||
| chr5:75435213
|
T | C | 1 | a0001c0001t0002g0185 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.349-8735A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435213 | ||||||
| chr5:75435234
|
C | T | 3 | a0001c0001t0002g0197a0001c0001t0002g0206a0001c0001t0002g0216 | 3 | HG00673.hp1 NA18941.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.349-8756G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435234 | ||||||
| chr5:75435326
|
C | T | 1 | a0001c0002t0001g0011 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.349-8848G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435326 | ||||||
| chr5:75435369
|
T | G | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.349-8891A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435369 | ||||||
| chr5:75435679
|
C | T | 7 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-9201G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435679 | ||||||
| chr5:75435907
|
A | G | 170 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(167): Show | 170 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.349-9429T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435907 | ||||||
| chr5:75435915
|
T | A | 1 | a0001c0002t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.349-9437A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75435915 | ||||||
| chr5:75436003
|
G | C | 2 | a0001c0001t0012g0240a0001c0001t0012g0241 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349-9525C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436003 | ||||||
| chr5:75436090
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.349-9612G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436090 | ||||||
| chr5:75436177
|
C | T | 1 | a0001c0007t0001g0336 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.349-9699G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436177 | ||||||
| chr5:75436179
|
T | C | 165 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(162): Show | 165 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.349-9701A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436179 | ||||||
| chr5:75436186
|
C | G | 42 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(39): Show | 42 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-9708G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436186 | ||||||
| chr5:75436198
|
A | G | 24 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0097others(21): Show | 24 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-9720T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436198 | ||||||
| chr5:75436390
|
T | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-9912A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436390 | ||||||
| chr5:75436553
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-10075C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436553 | ||||||
| chr5:75436620
|
C | T | 77 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(74): Show | 77 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.349-10142G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75436620 | ||||||
| chr5:75437112
|
T | A | 14 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(11): Show | 14 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-10634A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437112 | ||||||
| chr5:75437193
|
A | G | 5 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-10715T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437193 | ||||||
| chr5:75437661
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-11183C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437661 | ||||||
| chr5:75437768
|
TA | T | 71 | a0001c0001t0001g0036a0001c0001t0003g0303a0001c0001t0005g0278others(68): Show | 71 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.349-11291delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437768 | ||||||
| chr5:75437768
|
TAA | T | 13 | a0001c0002t0001g0038a0001c0002t0001g0064a0001c0002t0001g0065others(10): Show | 13 | HG02027.hp1 HG02040.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-11292_349-1129 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437768 | ||||||
| chr5:75437781
|
A | AG | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-11304_349-1130 others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437781 | ||||||
| chr5:75437786
|
A | G | 1 | a0001c0002t0001g0113 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.349-11308T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437786 | ||||||
| chr5:75437995
|
T | G | 2 | a0001c0001t0002g0142a0001c0001t0002g0156 | 2 | HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.349-11517A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75437995 | ||||||
| chr5:75438071
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-11593A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438071 | ||||||
| chr5:75438335
|
T | C | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.349-11857A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438335 | ||||||
| chr5:75438372
|
A | G | 1 | a0001c0002t0001g0052 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.349-11894T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438372 | ||||||
| chr5:75438408
|
A | C | 1 | a0001c0002t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.349-11930T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438408 | ||||||
| chr5:75438442
|
G | A | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.349-11964C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438442 | ||||||
| chr5:75438487
|
C | T | 4 | a0001c0002t0001g0089a0001c0002t0001g0094a0001c0002t0001g0095others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-12009G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438487 | ||||||
| chr5:75438537
|
A | G | 169 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(166): Show | 169 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.349-12059T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438537 | ||||||
| chr5:75438921
|
C | CT | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-12444dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438921 | ||||||
| chr5:75438932
|
T | TC | 80 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(77): Show | 80 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.349-12455dupG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438932 | ||||||
| chr5:75438969
|
AT | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-12492delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438969 | ||||||
| chr5:75438981
|
T | C | 3 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071 | 3 | NA19068.hp2 NA19075.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.349-12503A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75438981 | ||||||
| chr5:75439068
|
G | C | 2 | a0001c0002t0001g0084a0001c0002t0001g0085 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.349-12590C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75439068 | ||||||
| chr5:75439213
|
A | G | 169 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(166): Show | 169 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.349-12735T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75439213 | ||||||
| chr5:75439399
|
G | A | 1 | a0001c0001t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349-12921C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75439399 | ||||||
| chr5:75439738
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-13260C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75439738 | ||||||
| chr5:75439936
|
A | C | 2 | a0001c0001t0005g0278a0001c0001t0005g0279 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.349-13458T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75439936 | ||||||
| chr5:75440050
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-13572T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440050 | ||||||
| chr5:75440058
|
T | C | 1 | a0001c0002t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.349-13580A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440058 | ||||||
| chr5:75440231
|
A | G | 1 | a0001c0002t0009g0323 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.349-13753T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440231 | ||||||
| chr5:75440240
|
A | C | 177 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(174): Show | 177 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.349-13762T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440240 | ||||||
| chr5:75440274
|
T | C | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.349-13796A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440274 | ||||||
| chr5:75440333
|
A | G | 1 | a0001c0002t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.349-13855T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440333 | ||||||
| chr5:75440565
|
GAACATGC others(5): Show |
G | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.349-14099_349-1408 others(16): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440565 | ||||||
| chr5:75440625
|
T | G | 1 | a0001c0001t0013g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.349-14147A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440625 | ||||||
| chr5:75440735
|
A | G | 2 | a0001c0002t0001g0083a0001c0002t0001g0248 | 2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.349-14257T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440735 | ||||||
| chr5:75440775
|
TA | T | 234 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(231): Show | 234 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.349-14298delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440775 | ||||||
| chr5:75440829
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349-14351C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440829 | ||||||
| chr5:75440927
|
C | G | 1 | a0001c0001t0012g0241 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.349-14449G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75440927 | ||||||
| chr5:75441159
|
C | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-14681G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75441159 | ||||||
| chr5:75441469
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-14991C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75441469 | ||||||
| chr5:75441591
|
T | TA | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-15114dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75441591 | ||||||
| chr5:75441686
|
T | C | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.349-15208A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75441686 | ||||||
| chr5:75441794
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.349-15316C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75441794 | ||||||
| chr5:75441920
|
C | A | 2 | a0001c0001t0007g0186a0001c0001t0007g0226 | 2 | NA18949.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.349-15442G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75441920 | ||||||
| chr5:75442318
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.349-15840G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75442318 | ||||||
| chr5:75442545
|
T | C | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-16067A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75442545 | ||||||
| chr5:75442857
|
G | A | 5 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+16208C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75442857 | ||||||
| chr5:75442867
|
T | C | 1 | a0001c0002t0009g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.348+16198A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75442867 | ||||||
| chr5:75442934
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.348+16131C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75442934 | ||||||
| chr5:75443331
|
G | A | 23 | a0001c0001t0002g0135a0001c0001t0002g0138a0001c0001t0002g0139others(20): Show | 23 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.348+15734C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75443331 | ||||||
| chr5:75443456
|
T | C | 1 | a0001c0002t0001g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+15609A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75443456 | ||||||
| chr5:75443477
|
A | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.348+15588T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75443477 | ||||||
| chr5:75443712
|
T | A | 1 | a0001c0001t0002g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.348+15353A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75443712 | ||||||
| chr5:75443862
|
C | A | 1 | a0001c0001t0002g0250 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.348+15203G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75443862 | ||||||
| chr5:75444039
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+15026G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444039 | ||||||
| chr5:75444160
|
A | T | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.348+14905T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444160 | ||||||
| chr5:75444204
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+14861G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444204 | ||||||
| chr5:75444548
|
C | CT | 29 | a0001c0001t0001g0036a0001c0001t0002g0122a0001c0001t0002g0196others(26): Show | 29 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+14516dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444548 | ||||||
| chr5:75444553
|
T | C | 1 | a0001c0001t0002g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.348+14512A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444553 | ||||||
| chr5:75444615
|
C | T | 1 | a0001c0001t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+14450G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444615 | ||||||
| chr5:75444931
|
C | T | 76 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(73): Show | 76 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+14134G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75444931 | ||||||
| chr5:75445023
|
A | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+14042T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445023 | ||||||
| chr5:75445125
|
C | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.348+13940G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445125 | ||||||
| chr5:75445164
|
T | C | 1 | a0001c0002t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.348+13901A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445164 | ||||||
| chr5:75445220
|
T | C | 4 | a0001c0001t0002g0190a0001c0001t0002g0199a0001c0001t0002g0201others(1): Show | 4 | NA18977.hp2 NA18995.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+13845A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445220 | ||||||
| chr5:75445259
|
A | G | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+13806T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445259 | ||||||
| chr5:75445526
|
A | AT | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+13538dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445526 | ||||||
| chr5:75445652
|
G | T | 4 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(1): Show | 4 | NA18948.hp2 NA18991.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+13413C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445652 | ||||||
| chr5:75445939
|
T | C | 10 | a0001c0002t0001g0009a0001c0002t0001g0031a0001c0002t0001g0040others(7): Show | 10 | HG00741.hp1 HG01943.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+13126A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75445939 | ||||||
| chr5:75446032
|
CAT | C | 7 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0064others(4): Show | 7 | HG02040.hp2 HG03490.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+13031_348+1303 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75446032 | ||||||
| chr5:75446046
|
T | C | 42 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(39): Show | 42 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+13019A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75446046 | ||||||
| chr5:75446667
|
T | A | 1 | a0001c0001t0006g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+12398A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75446667 | ||||||
| chr5:75446677
|
C | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.348+12388G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75446677 | ||||||
| chr5:75446820
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.348+12245T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75446820 | ||||||
| chr5:75447072
|
T | C | 1 | a0001c0001t0006g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.348+11993A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447072 | ||||||
| chr5:75447263
|
A | T | 1 | a0001c0001t0002g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.348+11802T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447263 | ||||||
| chr5:75447445
|
A | AATTT | 8 | a0001c0001t0002g0164a0001c0001t0011g0158a0001c0001t0011g0161others(5): Show | 8 | HG03139.hp1 HG03195.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+11616_348+1161 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447445 | ||||||
| chr5:75447445
|
A | AATTTATT others(1): Show |
31 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(28): Show | 31 | HG00735.hp1 HG01081.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.348+11612_348+1161 others(12): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447445 | ||||||
| chr5:75447445
|
A | AATTTATT others(5): Show |
31 | a0001c0001t0003g0172a0001c0001t0003g0304a0001c0001t0013g0243others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.348+11608_348+1161 others(16): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447445 | ||||||
| chr5:75447445
|
A | AATTTATT others(9): Show |
12 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(9): Show | 12 | HG00642.hp1 HG01516.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.348+11604_348+1161 others(20): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447445 | ||||||
| chr5:75447445
|
A | AATTTATT others(13): Show |
2 | a0001c0001t0013g0258a0001c0002t0001g0098 | 2 | HG02258.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.348+11600_348+1161 others(24): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447445 | ||||||
| chr5:75447445
|
AATTT | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.348+11616_348+1161 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447445 | ||||||
| chr5:75447474
|
A | T | 1 | a0001c0001t0002g0127 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.348+11591T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447474 | ||||||
| chr5:75447474
|
ATTT | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+11588_348+1159 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447474 | ||||||
| chr5:75447478
|
T | A | 1 | a0001c0002t0022g0014 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.348+11587A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447478 | ||||||
| chr5:75447624
|
C | A | 1 | a0001c0001t0012g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.348+11441G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447624 | ||||||
| chr5:75447627
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.348+11438G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447627 | ||||||
| chr5:75447668
|
G | A | 1 | a0001c0002t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.348+11397C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447668 | ||||||
| chr5:75447709
|
C | T | 14 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(11): Show | 14 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+11356G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447709 | ||||||
| chr5:75447715
|
C | T | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+11350G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447715 | ||||||
| chr5:75447728
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+11337G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447728 | ||||||
| chr5:75447854
|
TAGCCTCA others(6): Show |
T | 1 | a0001c0002t0018g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.348+11198_348+1121 others(17): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447854 | ||||||
| chr5:75447918
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+11147C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75447918 | ||||||
| chr5:75448356
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.348+10709A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75448356 | ||||||
| chr5:75448379
|
A | C | 1 | a0001c0002t0004g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.348+10686T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75448379 | ||||||
| chr5:75448490
|
A | G | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+10575T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75448490 | ||||||
| chr5:75448773
|
T | C | 1 | a0001c0002t0001g0055 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.348+10292A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75448773 | ||||||
| chr5:75448896
|
T | G | 29 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0172others(26): Show | 29 | HG00642.hp1 HG01192.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.348+10169A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75448896 | ||||||
| chr5:75448918
|
G | T | 1 | a0001c0001t0002g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.348+10147C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75448918 | ||||||
| chr5:75449031
|
A | T | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+10034T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449031 | ||||||
| chr5:75449056
|
T | A | 1 | a0001c0001t0011g0161 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.348+10009A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449056 | ||||||
| chr5:75449064
|
C | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.348+10001G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449064 | ||||||
| chr5:75449258
|
G | A | 8 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+9807C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449258 | ||||||
| chr5:75449324
|
T | C | 1 | a0001c0002t0001g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.348+9741A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449324 | ||||||
| chr5:75449403
|
G | T | 152 | a0001c0001t0001g0036a0001c0001t0003g0120a0001c0001t0003g0131others(149): Show | 152 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.348+9662C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449403 | ||||||
| chr5:75449417
|
G | A | 1 | a0001c0002t0004g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.348+9648C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449417 | ||||||
| chr5:75449620
|
T | C | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.348+9445A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449620 | ||||||
| chr5:75449664
|
G | C | 4 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0206others(1): Show | 4 | HG00673.hp1 NA18747.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+9401C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449664 | ||||||
| chr5:75449696
|
TTGG | T | 71 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(68): Show | 71 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.348+9366_348+9368d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449696 | ||||||
| chr5:75449707
|
GT | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+9357delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449707 | ||||||
| chr5:75449719
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.348+9346T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449719 | ||||||
| chr5:75449806
|
T | G | 1 | a0001c0001t0002g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.348+9259A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449806 | ||||||
| chr5:75449830
|
T | C | 1 | a0001c0002t0004g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.348+9235A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75449830 | ||||||
| chr5:75450030
|
C | T | 1 | a0001c0001t0012g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.348+9035G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75450030 | ||||||
| chr5:75450401
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.348+8664T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75450401 | ||||||
| chr5:75450561
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+8504C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75450561 | ||||||
| chr5:75450813
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+8252A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75450813 | ||||||
| chr5:75451047
|
A | G | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+8018T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451047 | ||||||
| chr5:75451055
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.348+8010C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451055 | ||||||
| chr5:75451171
|
T | A | 1 | a0001c0001t0002g0250 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.348+7894A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451171 | ||||||
| chr5:75451377
|
T | C | 33 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(30): Show | 33 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.348+7688A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451377 | ||||||
| chr5:75451642
|
G | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+7423C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451642 | ||||||
| chr5:75451661
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+7404T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451661 | ||||||
| chr5:75451671
|
A | G | 2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.348+7394T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451671 | ||||||
| chr5:75451705
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.348+7360G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451705 | ||||||
| chr5:75451892
|
T | C | 3 | a0001c0001t0003g0175a0001c0001t0003g0177a0001c0001t0003g0180 | 3 | HG02055.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.348+7173A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451892 | ||||||
| chr5:75451964
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.348+7101C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75451964 | ||||||
| chr5:75452355
|
G | T | 2 | a0001c0002t0001g0037a0001c0002t0004g0018 | 2 | HG01257.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.348+6710C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75452355 | ||||||
| chr5:75452571
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.348+6494C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75452571 | ||||||
| chr5:75452649
|
T | C | 33 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(30): Show | 33 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.348+6416A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75452649 | ||||||
| chr5:75452680
|
C | T | 242 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(239): Show | 242 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.348+6385G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75452680 | ||||||
| chr5:75452871
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.348+6194A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75452871 | ||||||
| chr5:75453014
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+6051G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453014 | ||||||
| chr5:75453137
|
C | T | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.348+5928G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453137 | ||||||
| chr5:75453509
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0181a0001c0001t0002g0182 | 3 | HG01192.hp1 HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.348+5556G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453509 | ||||||
| chr5:75453542
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.348+5523T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453542 | ||||||
| chr5:75453800
|
T | C | 2 | a0001c0001t0002g0166a0001c0001t0002g0168 | 2 | NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.348+5265A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453800 | ||||||
| chr5:75453812
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+5253C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453812 | ||||||
| chr5:75453814
|
G | C | 78 | a0001c0001t0001g0036a0001c0001t0003g0120a0001c0002t0001g0009others(75): Show | 78 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.348+5251C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453814 | ||||||
| chr5:75453825
|
TGA | T | 327 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.348+5238_348+5239d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75453825 | ||||||
| chr5:75454082
|
T | A | 1 | a0001c0001t0008g0309 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.348+4983A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454082 | ||||||
| chr5:75454144
|
T | C | 2 | a0001c0001t0002g0202a0001c0001t0002g0249 | 2 | HG00099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.348+4921A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454144 | ||||||
| chr5:75454446
|
T | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+4619A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454446 | ||||||
| chr5:75454567
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.348+4498G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454567 | ||||||
| chr5:75454734
|
C | T | 2 | a0001c0001t0002g0121a0001c0001t0002g0125 | 2 | NA18942.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.348+4331G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454734 | ||||||
| chr5:75454817
|
G | A | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+4248C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454817 | ||||||
| chr5:75454969
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.348+4096T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75454969 | ||||||
| chr5:75455106
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+3959G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455106 | ||||||
| chr5:75455117
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.348+3948C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455117 | ||||||
| chr5:75455177
|
CT | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+3887delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455177 | ||||||
| chr5:75455222
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.348+3843A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455222 | ||||||
| chr5:75455289
|
C | A | 1 | a0001c0002t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.348+3776G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455289 | ||||||
| chr5:75455314
|
G | A | 1 | a0001c0001t0005g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+3751C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455314 | ||||||
| chr5:75455366
|
T | C | 1 | a0001c0001t0002g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.348+3699A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455366 | ||||||
| chr5:75455375
|
G | A | 7 | a0001c0001t0011g0230a0001c0002t0009g0323a0001c0002t0009g0324others(4): Show | 7 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+3690C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455375 | ||||||
| chr5:75455723
|
T | G | 1 | a0001c0001t0002g0220 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.348+3342A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455723 | ||||||
| chr5:75455763
|
G | A | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+3302C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75455763 | ||||||
| chr5:75456288
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+2777T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456288 | ||||||
| chr5:75456389
|
C | T | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+2676G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456389 | ||||||
| chr5:75456452
|
T | C | 8 | a0001c0001t0002g0225a0001c0001t0002g0227a0001c0001t0007g0173others(5): Show | 8 | HG00735.hp2 HG02165.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+2613A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456452 | ||||||
| chr5:75456572
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+2493C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456572 | ||||||
| chr5:75456589
|
G | A | 3 | a0001c0001t0005g0274a0001c0001t0005g0275a0001c0001t0005g0276 | 3 | HG00741.hp2 HG01106.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.348+2476C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456589 | ||||||
| chr5:75456655
|
C | T | 1 | a0001c0001t0007g0228 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.348+2410G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456655 | ||||||
| chr5:75456663
|
CA | C | 206 | a0001c0001t0001g0036a0001c0001t0001g0311a0001c0001t0001g0312others(203): Show | 206 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.348+2401delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456663 | ||||||
| chr5:75456663
|
CAA | C | 18 | a0001c0001t0001g0310a0001c0001t0002g0147a0001c0001t0003g0305others(15): Show | 18 | HG01069.hp1 HG01081.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.348+2400_348+2401d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456663 | ||||||
| chr5:75456663
|
CAAA | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+2399_348+2401d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456663 | ||||||
| chr5:75456683
|
A | G | 2 | a0001c0001t0008g0267a0001c0001t0008g0309 | 2 | HG01981.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.348+2382T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456683 | ||||||
| chr5:75456756
|
T | C | 1 | a0001c0001t0002g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.348+2309A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456756 | ||||||
| chr5:75456757
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.348+2308G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456757 | ||||||
| chr5:75456819
|
C | T | 2 | a0001c0001t0002g0142a0001c0002t0004g0008 | 2 | HG03669.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.348+2246G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456819 | ||||||
| chr5:75456833
|
T | C | 12 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.348+2232A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75456833 | ||||||
| chr5:75457137
|
A | G | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.348+1928T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457137 | ||||||
| chr5:75457165
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+1900G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457165 | ||||||
| chr5:75457233
|
G | C | 1 | a0001c0001t0003g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.348+1832C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457233 | ||||||
| chr5:75457254
|
T | C | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+1811A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457254 | ||||||
| chr5:75457421
|
G | A | 1 | a0001c0001t0011g0230 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.348+1644C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457421 | ||||||
| chr5:75457442
|
T | C | 1 | a0001c0002t0021g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.348+1623A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457442 | ||||||
| chr5:75457448
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.348+1617A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457448 | ||||||
| chr5:75457457
|
T | C | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.348+1608A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457457 | ||||||
| chr5:75457578
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.348+1487T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457578 | ||||||
| chr5:75457809
|
A | G | 67 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(64): Show | 67 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.348+1256T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457809 | ||||||
| chr5:75457827
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1238T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457827 | ||||||
| chr5:75457829
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.348+1236G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457829 | ||||||
| chr5:75457870
|
G | A | 1 | a0001c0002t0001g0011 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.348+1195C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457870 | ||||||
| chr5:75457909
|
C | CGT | 15 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(12): Show | 15 | HG02027.hp2 HG02723.hp2 HG03471.hp1 others(12): Show |
intron_variant | MODIFIER | c.348+1154_348+1155d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457909 | ||||||
| chr5:75457909
|
CGTGT | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.348+1152_348+1155d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457909 | ||||||
| chr5:75457911
|
T | C | 86 | a0001c0001t0001g0036a0001c0001t0001g0321a0001c0001t0002g0232others(83): Show | 86 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.348+1154A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457911 | ||||||
| chr5:75457913
|
T | C | 7 | a0001c0002t0001g0028a0001c0002t0001g0032a0001c0002t0001g0041others(4): Show | 7 | HG02040.hp2 HG02970.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+1152A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457913 | ||||||
| chr5:75457922
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+1143C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457922 | ||||||
| chr5:75457959
|
ATG | A | 299 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.348+1104_348+1105d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457959 | ||||||
| chr5:75457959
|
ATGTG | A | 9 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+1102_348+1105d others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457959 | ||||||
| chr5:75457970
|
T | TGTGTGTG others(2): Show |
8 | a0001c0001t0006g0134a0001c0001t0006g0234a0001c0001t0006g0235others(5): Show | 8 | HG01081.hp2 HG01891.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1086_348+1094d others(11): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457970 | ||||||
| chr5:75457970
|
T | TGTGTGTG others(4): Show |
2 | a0001c0001t0006g0233a0001c0006t0006g0268 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.348+1084_348+1094d others(13): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457970 | ||||||
| chr5:75457984
|
ATG | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1079_348+1080d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457984 | ||||||
| chr5:75457986
|
G | A | 10 | a0001c0001t0006g0134a0001c0001t0006g0233a0001c0001t0006g0234others(7): Show | 10 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+1079C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75457986 | ||||||
| chr5:75458111
|
C | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+954G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458111 | ||||||
| chr5:75458156
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.348+909A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458156 | ||||||
| chr5:75458289
|
A | G | 2 | a0001c0001t0006g0233a0001c0006t0006g0268 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.348+776T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458289 | ||||||
| chr5:75458407
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+658C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458407 | ||||||
| chr5:75458521
|
A | G | 2 | a0001c0002t0001g0074a0001c0002t0001g0075 | 2 | NA18964.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.348+544T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458521 | ||||||
| chr5:75458530
|
A | T | 122 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(119): Show | 122 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.348+535T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458530 | ||||||
| chr5:75458557
|
C | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.348+508G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458557 | ||||||
| chr5:75458629
|
G | A | 1 | a0001c0001t0002g0220 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.348+436C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458629 | ||||||
| chr5:75458650
|
C | T | 1 | a0001c0001t0003g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.348+415G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458650 | ||||||
| chr5:75458819
|
G | C | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+246C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458819 | ||||||
| chr5:75458878
|
T | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.348+187A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75458878 | ||||||
| chr5:75459017
|
A | T | 1 | a0001c0002t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.348+48T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 3/16 | chr5 | 75459017 | ||||||
| chr5:75459203
|
T | C | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-22A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459203 | ||||||
| chr5:75459413
|
T | G | 1 | a0001c0001t0013g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232-232A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459413 | ||||||
| chr5:75459623
|
A | G | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-442T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459623 | ||||||
| chr5:75459789
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-608G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459789 | ||||||
| chr5:75459889
|
G | A | 2 | a0001c0001t0003g0242a0001c0001t0003g0246 | 2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.232-708C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459889 | ||||||
| chr5:75459947
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.232-766C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459947 | ||||||
| chr5:75459962
|
C | CA | 44 | a0001c0001t0002g0130a0001c0001t0002g0146a0001c0001t0002g0150others(41): Show | 44 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.232-782dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459962 | ||||||
| chr5:75459962
|
C | CAA | 9 | a0001c0001t0003g0288a0001c0001t0003g0289a0001c0001t0003g0290others(6): Show | 9 | HG00544.hp2 HG01243.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.232-783_232-782dup others(2): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459962 | ||||||
| chr5:75459962
|
CA | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0319a0001c0001t0002g0148others(14): Show | 17 | HG01167.hp1 HG01256.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.232-782delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75459962 | ||||||
| chr5:75460229
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.232-1048G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460229 | ||||||
| chr5:75460257
|
C | T | 3 | a0001c0002t0001g0110a0001c0002t0001g0114a0001c0007t0001g0336 | 3 | HG03704.hp2 NA18747.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.232-1076G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460257 | ||||||
| chr5:75460258
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.232-1077T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460258 | ||||||
| chr5:75460293
|
T | C | 82 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(79): Show | 82 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.232-1112A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460293 | ||||||
| chr5:75460385
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-1204T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460385 | ||||||
| chr5:75460396
|
A | G | 81 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(78): Show | 81 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.232-1215T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460396 | ||||||
| chr5:75460404
|
T | C | 1 | a0001c0002t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.232-1223A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460404 | ||||||
| chr5:75460662
|
C | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-1481G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460662 | ||||||
| chr5:75460823
|
C | T | 1 | a0001c0001t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.232-1642G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75460823 | ||||||
| chr5:75461282
|
T | C | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.232-2101A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461282 | ||||||
| chr5:75461303
|
G | A | 1 | a0001c0002t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.232-2122C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461303 | ||||||
| chr5:75461461
|
G | A | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.232-2280C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461461 | ||||||
| chr5:75461591
|
G | C | 1 | a0001c0002t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.232-2410C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461591 | ||||||
| chr5:75461712
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-2531A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461712 | ||||||
| chr5:75461731
|
G | A | 247 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(244): Show | 247 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.232-2550C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461731 | ||||||
| chr5:75461821
|
G | GA | 98 | a0001c0001t0001g0036a0001c0001t0001g0317a0001c0001t0002g0166others(95): Show | 98 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.232-2641dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461821 | ||||||
| chr5:75461821
|
GA | G | 17 | a0001c0001t0001g0312a0001c0001t0002g0188a0001c0001t0002g0202others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.232-2641delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461821 | ||||||
| chr5:75461832
|
A | C | 33 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(30): Show | 33 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.232-2651T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461832 | ||||||
| chr5:75461933
|
T | C | 47 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(44): Show | 47 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.232-2752A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75461933 | ||||||
| chr5:75462132
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-2951A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462132 | ||||||
| chr5:75462236
|
A | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | NA18953.hp1 NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.232-3055T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462236 | ||||||
| chr5:75462284
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.232-3103A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462284 | ||||||
| chr5:75462948
|
C | A | 1 | a0003c0004t0003g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232-3767G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462948 | ||||||
| chr5:75462949
|
G | A | 1 | a0001c0001t0005g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.232-3768C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462949 | ||||||
| chr5:75462977
|
C | A | 1 | a0001c0002t0001g0033 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232-3796G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462977 | ||||||
| chr5:75462988
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.232-3807G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462988 | ||||||
| chr5:75462990
|
C | CA | 27 | a0001c0001t0002g0144a0001c0001t0002g0150a0001c0001t0002g0154others(24): Show | 27 | HG00621.hp1 HG01255.hp1 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.232-3810dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462990 | ||||||
| chr5:75462990
|
C | CAA | 30 | a0001c0001t0001g0311a0001c0001t0003g0131a0001c0001t0003g0172others(27): Show | 30 | HG00642.hp1 HG01192.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.232-3811_232-3810d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462990 | ||||||
| chr5:75462990
|
C | CAAA | 11 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(8): Show | 11 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.232-3812_232-3810d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462990 | ||||||
| chr5:75462990
|
CA | C | 16 | a0001c0001t0001g0036a0001c0002t0001g0028a0001c0002t0001g0037others(13): Show | 16 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.232-3810delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75462990 | ||||||
| chr5:75463358
|
T | A | 242 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(239): Show | 242 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.232-4177A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75463358 | ||||||
| chr5:75463510
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.232-4329C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75463510 | ||||||
| chr5:75463513
|
C | T | 1 | a0001c0001t0016g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.232-4332G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75463513 | ||||||
| chr5:75463711
|
T | C | 3 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0277 | 3 | HG01167.hp2 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.232-4530A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75463711 | ||||||
| chr5:75463750
|
A | G | 1 | a0001c0001t0014g0238 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232-4569T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75463750 | ||||||
| chr5:75464144
|
T | C | 1 | a0001c0001t0003g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.232-4963A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464144 | ||||||
| chr5:75464173
|
A | C | 1 | a0001c0002t0001g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.232-4992T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464173 | ||||||
| chr5:75464210
|
A | G | 1 | a0001c0001t0002g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.232-5029T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464210 | ||||||
| chr5:75464359
|
G | GCCA | 169 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(166): Show | 169 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.232-5179_232-5178i others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464359 | ||||||
| chr5:75464380
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-5199A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464380 | ||||||
| chr5:75464447
|
G | T | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-5266C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464447 | ||||||
| chr5:75464681
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-5500A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464681 | ||||||
| chr5:75464698
|
C | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-5517G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464698 | ||||||
| chr5:75464806
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.232-5625C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464806 | ||||||
| chr5:75464858
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-5677T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464858 | ||||||
| chr5:75464918
|
C | A | 6 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0277others(3): Show | 6 | HG01167.hp2 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-5737G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75464918 | ||||||
| chr5:75465255
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232-6074G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465255 | ||||||
| chr5:75465384
|
C | A | 1 | a0001c0002t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.232-6203G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465384 | ||||||
| chr5:75465534
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-6353T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465534 | ||||||
| chr5:75465852
|
G | A | 1 | a0001c0002t0001g0082 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.232-6671C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465852 | ||||||
| chr5:75465948
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-6767A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465948 | ||||||
| chr5:75465957
|
G | A | 2 | a0001c0001t0012g0240a0001c0001t0012g0241 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.232-6776C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465957 | ||||||
| chr5:75465987
|
T | C | 1 | a0001c0002t0001g0113 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.232-6806A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75465987 | ||||||
| chr5:75466170
|
T | C | 1 | a0001c0002t0022g0014 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.232-6989A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466170 | ||||||
| chr5:75466346
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-7165T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466346 | ||||||
| chr5:75466385
|
C | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-7204G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466385 | ||||||
| chr5:75466386
|
G | A | 2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.232-7205C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466386 | ||||||
| chr5:75466390
|
G | T | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-7209C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466390 | ||||||
| chr5:75466421
|
C | T | 10 | a0001c0001t0006g0134a0001c0001t0006g0233a0001c0001t0006g0234others(7): Show | 10 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-7240G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466421 | ||||||
| chr5:75466455
|
C | A | 182 | a0001c0001t0001g0036a0001c0001t0003g0120a0001c0001t0003g0131others(179): Show | 182 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.232-7274G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466455 | ||||||
| chr5:75466500
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-7319C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466500 | ||||||
| chr5:75466667
|
C | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-7486G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466667 | ||||||
| chr5:75466753
|
A | T | 23 | a0001c0001t0003g0131a0001c0001t0003g0172a0001c0001t0003g0175others(20): Show | 23 | HG00642.hp1 HG01192.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.232-7572T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75466753 | ||||||
| chr5:75467026
|
T | C | 1 | a0001c0002t0004g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.232-7845A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467026 | ||||||
| chr5:75467063
|
AC | A | 6 | a0001c0002t0001g0028a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG02040.hp2 HG03490.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-7883delG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467063 | ||||||
| chr5:75467073
|
C | T | 31 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.232-7892G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467073 | ||||||
| chr5:75467220
|
T | C | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | NA18956.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.232-8039A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467220 | ||||||
| chr5:75467247
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-8066G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467247 | ||||||
| chr5:75467298
|
G | A | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232-8117C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467298 | ||||||
| chr5:75467335
|
G | A | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.232-8154C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467335 | ||||||
| chr5:75467462
|
G | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232-8281C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467462 | ||||||
| chr5:75467641
|
C | CA | 24 | a0001c0001t0002g0187a0001c0002t0001g0089a0001c0002t0001g0091others(21): Show | 24 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.232-8461dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467641 | ||||||
| chr5:75467641
|
C | CAA | 7 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0092others(4): Show | 7 | HG02602.hp1 HG02738.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.232-8462_232-8461d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467641 | ||||||
| chr5:75467650
|
G | A | 40 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(37): Show | 40 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.232-8469C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467650 | ||||||
| chr5:75467650
|
G | GA | 144 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.232-8470dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467650 | ||||||
| chr5:75467650
|
G | GAA | 47 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(44): Show | 47 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.232-8471_232-8470d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467650 | ||||||
| chr5:75467650
|
GA | G | 69 | a0001c0001t0012g0241a0001c0002t0001g0009a0001c0002t0001g0010others(66): Show | 69 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.232-8470delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467650 | ||||||
| chr5:75467650
|
GAA | G | 9 | a0001c0001t0001g0036a0001c0001t0012g0240a0001c0002t0001g0329others(6): Show | 9 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.232-8471_232-8470d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467650 | ||||||
| chr5:75467655
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.232-8474T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75467655 | ||||||
| chr5:75468131
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-8950G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468131 | ||||||
| chr5:75468170
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.232-8989G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468170 | ||||||
| chr5:75468291
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-9110A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468291 | ||||||
| chr5:75468457
|
C | T | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-9276G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468457 | ||||||
| chr5:75468522
|
T | C | 188 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(185): Show | 188 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.232-9341A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468522 | ||||||
| chr5:75468568
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.232-9387C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468568 | ||||||
| chr5:75468711
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-9530A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468711 | ||||||
| chr5:75468807
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-9626A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468807 | ||||||
| chr5:75468883
|
T | C | 1 | a0001c0001t0003g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232-9702A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468883 | ||||||
| chr5:75468905
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-9724G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468905 | ||||||
| chr5:75468950
|
C | A | 1 | a0001c0001t0002g0265 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.232-9769G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75468950 | ||||||
| chr5:75469137
|
CAG | C | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-9958_232-9957d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469137 | ||||||
| chr5:75469198
|
T | C | 1 | a0001c0002t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.232-10017A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469198 | ||||||
| chr5:75469246
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232-10065A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469246 | ||||||
| chr5:75469281
|
T | C | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-10100A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469281 | ||||||
| chr5:75469306
|
C | T | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.232-10125G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469306 | ||||||
| chr5:75469421
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-10240G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469421 | ||||||
| chr5:75469469
|
T | C | 35 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(32): Show | 35 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.232-10288A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469469 | ||||||
| chr5:75469552
|
A | AT | 78 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(75): Show | 78 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.232-10372dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469552 | ||||||
| chr5:75469553
|
T | TG | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-10373_232-1037 others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469553 | ||||||
| chr5:75469632
|
C | T | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.232-10451G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469632 | ||||||
| chr5:75469637
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232-10456C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469637 | ||||||
| chr5:75469731
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-10550G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469731 | ||||||
| chr5:75469754
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.232-10573C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469754 | ||||||
| chr5:75469904
|
G | C | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-10723C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75469904 | ||||||
| chr5:75470025
|
T | C | 1 | a0001c0001t0006g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.232-10844A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470025 | ||||||
| chr5:75470096
|
C | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-10915G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470096 | ||||||
| chr5:75470271
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.232-11090C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470271 | ||||||
| chr5:75470528
|
G | T | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.232-11347C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470528 | ||||||
| chr5:75470542
|
GAAAAAGC others(9): Show |
G | 1 | a0001c0001t0002g0284 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.232-11377_232-1136 others(20): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470542 | ||||||
| chr5:75470573
|
T | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.232-11392A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470573 | ||||||
| chr5:75470766
|
T | C | 2 | a0001c0001t0003g0242a0001c0001t0003g0246 | 2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.232-11585A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470766 | ||||||
| chr5:75470886
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-11705C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470886 | ||||||
| chr5:75470893
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-11712C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75470893 | ||||||
| chr5:75471199
|
C | T | 7 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.232-12018G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471199 | ||||||
| chr5:75471486
|
C | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-12305G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471486 | ||||||
| chr5:75471487
|
G | A | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-12306C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471487 | ||||||
| chr5:75471531
|
C | T | 1 | a0001c0001t0002g0200 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.232-12350G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471531 | ||||||
| chr5:75471754
|
C | CA | 56 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(53): Show | 56 | HG00597.hp2 HG00642.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.232-12574dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471754 | ||||||
| chr5:75471754
|
C | CAA | 37 | a0001c0001t0001g0317a0001c0001t0001g0321a0001c0001t0003g0180others(34): Show | 37 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.232-12575_232-1257 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471754 | ||||||
| chr5:75471754
|
CA | C | 12 | a0001c0001t0002g0193a0001c0001t0002g0199a0001c0002t0001g0027others(9): Show | 12 | HG01934.hp2 HG02735.hp1 HG03490.hp1 others(9): Show |
intron_variant | MODIFIER | c.232-12574delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471754 | ||||||
| chr5:75471851
|
A | G | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232-12670T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471851 | ||||||
| chr5:75471966
|
A | C | 8 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.232-12785T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75471966 | ||||||
| chr5:75472228
|
G | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-13047C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472228 | ||||||
| chr5:75472420
|
A | G | 10 | a0001c0001t0006g0134a0001c0001t0006g0233a0001c0001t0006g0234others(7): Show | 10 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-13239T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472420 | ||||||
| chr5:75472522
|
C | A | 247 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(244): Show | 247 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.232-13341G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472522 | ||||||
| chr5:75472689
|
C | G | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-13508G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472689 | ||||||
| chr5:75472877
|
A | C | 3 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0216 | 3 | HG00673.hp1 NA18747.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.232-13696T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472877 | ||||||
| chr5:75472916
|
T | C | 3 | a0001c0001t0002g0191a0001c0001t0002g0247a0001c0001t0002g0251 | 3 | HG00438.hp2 HG00544.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.232-13735A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472916 | ||||||
| chr5:75472951
|
T | G | 5 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-13770A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75472951 | ||||||
| chr5:75473078
|
A | AT | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-13898dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473078 | ||||||
| chr5:75473172
|
T | C | 2 | a0001c0002t0004g0060a0001c0002t0004g0061 | 2 | NA18984.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.232-13991A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473172 | ||||||
| chr5:75473264
|
T | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.232-14083A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473264 | ||||||
| chr5:75473280
|
C | A | 1 | a0001c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.232-14099G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473280 | ||||||
| chr5:75473403
|
G | T | 1 | a0001c0005t0002g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.232-14222C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473403 | ||||||
| chr5:75473407
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.232-14226T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473407 | ||||||
| chr5:75473429
|
T | A | 33 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(30): Show | 33 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.232-14248A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473429 | ||||||
| chr5:75473479
|
CAAAT | C | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.232-14302_232-1429 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473479 | ||||||
| chr5:75473512
|
C | A | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.232-14331G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473512 | ||||||
| chr5:75473535
|
A | G | 1 | a0001c0001t0003g0297 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.232-14354T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473535 | ||||||
| chr5:75473672
|
G | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-14491C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473672 | ||||||
| chr5:75473673
|
A | T | 1 | a0001c0002t0001g0020 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.232-14492T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473673 | ||||||
| chr5:75473749
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.232-14568T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473749 | ||||||
| chr5:75473806
|
A | G | 8 | a0001c0001t0002g0265a0001c0001t0008g0261a0001c0001t0008g0262others(5): Show | 8 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-14625T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473806 | ||||||
| chr5:75473875
|
A | T | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.232-14694T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75473875 | ||||||
| chr5:75474012
|
C | T | 8 | a0001c0001t0002g0265a0001c0001t0008g0261a0001c0001t0008g0262others(5): Show | 8 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-14831G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474012 | ||||||
| chr5:75474092
|
C | T | 3 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289 | 3 | HG02818.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232-14911G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474092 | ||||||
| chr5:75474164
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.232-14983A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474164 | ||||||
| chr5:75474429
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.232-15248C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474429 | ||||||
| chr5:75474503
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-15322C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474503 | ||||||
| chr5:75474542
|
A | G | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232-15361T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474542 | ||||||
| chr5:75474654
|
A | T | 5 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-15473T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474654 | ||||||
| chr5:75474818
|
GGAGTCTA others(29): Show |
G | 243 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(240): Show | 243 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.232-15673_232-1563 others(40): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474818 | ||||||
| chr5:75474875
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-15694C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474875 | ||||||
| chr5:75474996
|
G | A | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-15815C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75474996 | ||||||
| chr5:75475031
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.232-15850A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475031 | ||||||
| chr5:75475147
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.232-15966C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475147 | ||||||
| chr5:75475217
|
G | T | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-16036C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475217 | ||||||
| chr5:75475260
|
T | C | 1 | a0001c0002t0001g0072 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.232-16079A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475260 | ||||||
| chr5:75475268
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.232-16087A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475268 | ||||||
| chr5:75475562
|
G | A | 82 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(79): Show | 82 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.232-16381C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475562 | ||||||
| chr5:75475571
|
G | A | 4 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(1): Show | 4 | NA18612.hp2 NA18979.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-16390C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475571 | ||||||
| chr5:75475590
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.232-16409T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475590 | ||||||
| chr5:75475590
|
A | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.232-16409T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475590 | ||||||
| chr5:75475674
|
G | A | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.232-16493C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475674 | ||||||
| chr5:75475695
|
C | CT | 43 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(40): Show | 43 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.232-16515dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475695 | ||||||
| chr5:75475757
|
T | C | 1 | a0001c0002t0022g0014 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.232-16576A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475757 | ||||||
| chr5:75475818
|
T | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | NA18953.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.232-16637A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475818 | ||||||
| chr5:75475939
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-16758G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75475939 | ||||||
| chr5:75476158
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-16977G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476158 | ||||||
| chr5:75476325
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-17144T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476325 | ||||||
| chr5:75476378
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.232-17197G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476378 | ||||||
| chr5:75476407
|
G | C | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.232-17226C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476407 | ||||||
| chr5:75476696
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.232-17515A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476696 | ||||||
| chr5:75476751
|
A | G | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-17570T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476751 | ||||||
| chr5:75476804
|
T | C | 1 | a0001c0002t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.232-17623A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476804 | ||||||
| chr5:75476841
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.232-17660G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476841 | ||||||
| chr5:75476842
|
G | GT | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-17662dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476842 | ||||||
| chr5:75476876
|
A | G | 2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.232-17695T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476876 | ||||||
| chr5:75476915
|
A | G | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-17734T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75476915 | ||||||
| chr5:75477038
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-17857C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477038 | ||||||
| chr5:75477050
|
T | C | 8 | a0001c0001t0002g0136a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 8 | NA18948.hp1 NA18953.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-17869A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477050 | ||||||
| chr5:75477211
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.232-18030C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477211 | ||||||
| chr5:75477483
|
A | G | 8 | a0001c0001t0002g0265a0001c0001t0008g0261a0001c0001t0008g0262others(5): Show | 8 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-18302T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477483 | ||||||
| chr5:75477595
|
T | C | 247 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(244): Show | 247 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.232-18414A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477595 | ||||||
| chr5:75477645
|
T | G | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.232-18464A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477645 | ||||||
| chr5:75477647
|
T | TA | 124 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(121): Show | 124 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.232-18467dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477647 | ||||||
| chr5:75477647
|
T | TAA | 53 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0164others(50): Show | 53 | HG00741.hp2 HG01106.hp2 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.232-18468_232-1846 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477647 | ||||||
| chr5:75477647
|
TA | T | 24 | a0001c0001t0002g0190a0001c0001t0002g0239a0001c0001t0003g0172others(21): Show | 24 | HG00642.hp1 HG01192.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.232-18467delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477647 | ||||||
| chr5:75477670
|
C | A | 1 | a0001c0001t0002g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.232-18489G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75477670 | ||||||
| chr5:75478050
|
C | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232-18869G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478050 | ||||||
| chr5:75478092
|
C | G | 1 | a0001c0001t0010g0001 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.232-18911G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478092 | ||||||
| chr5:75478133
|
C | G | 1 | a0001c0002t0001g0024 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.232-18952G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478133 | ||||||
| chr5:75478180
|
G | A | 28 | a0001c0001t0003g0131a0001c0001t0003g0172a0001c0001t0003g0175others(25): Show | 28 | HG00642.hp1 HG01192.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.232-18999C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478180 | ||||||
| chr5:75478203
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.232-19022T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478203 | ||||||
| chr5:75478240
|
T | G | 156 | a0001c0001t0001g0036a0001c0001t0003g0131a0001c0001t0003g0172others(153): Show | 156 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.232-19059A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478240 | ||||||
| chr5:75478314
|
TA | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-19134delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478314 | ||||||
| chr5:75478403
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-19222G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478403 | ||||||
| chr5:75478528
|
A | G | 1 | a0001c0002t0001g0078 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.232-19347T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478528 | ||||||
| chr5:75478656
|
T | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-19475A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478656 | ||||||
| chr5:75478831
|
G | C | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232-19650C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478831 | ||||||
| chr5:75478909
|
T | TA | 59 | a0001c0001t0002g0005a0001c0001t0002g0125a0001c0001t0002g0126others(56): Show | 59 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.232-19729dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
T | TAA | 24 | a0001c0001t0001g0310a0001c0001t0002g0167a0001c0001t0002g0168others(21): Show | 24 | HG00544.hp1 HG00621.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.232-19730_232-1972 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
T | TAAA | 17 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(14): Show | 17 | HG00642.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.232-19731_232-1972 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
T | TAAAA | 10 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(7): Show | 10 | HG01081.hp1 HG01261.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-19732_232-1972 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
TA | T | 10 | a0001c0002t0001g0090a0001c0002t0001g0098a0001c0002t0001g0111others(7): Show | 10 | HG01123.hp2 HG02486.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-19729delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
TAA | T | 24 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.232-19730_232-1972 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
TAAAA | T | 10 | a0001c0002t0001g0009a0001c0002t0001g0016a0001c0002t0001g0017others(7): Show | 10 | HG01934.hp2 HG02145.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-19732_232-1972 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
TAAAAA | T | 56 | a0001c0001t0001g0036a0001c0002t0001g0010a0001c0002t0001g0011others(53): Show | 56 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.232-19733_232-1972 others(9): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
TAAAAAA | T | 15 | a0001c0002t0001g0028a0001c0002t0001g0031a0001c0002t0001g0032others(12): Show | 15 | HG01169.hp1 HG01256.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.232-19734_232-1972 others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478909
|
TAAAAAAA others(1): Show |
T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-19736_232-1972 others(12): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478909 | ||||||
| chr5:75478971
|
T | G | 1 | a0001c0001t0002g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.232-19790A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478971 | ||||||
| chr5:75478980
|
A | C | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.232-19799T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75478980 | ||||||
| chr5:75479082
|
C | G | 1 | a0001c0002t0001g0030 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.232-19901G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479082 | ||||||
| chr5:75479103
|
C | CA | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.232-19923dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479103 | ||||||
| chr5:75479103
|
CA | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-19923delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479103 | ||||||
| chr5:75479653
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.232-20472A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479653 | ||||||
| chr5:75479799
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.232-20618T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479799 | ||||||
| chr5:75479893
|
T | C | 1 | a0001c0002t0001g0017 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.232-20712A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479893 | ||||||
| chr5:75479926
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.232-20745G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479926 | ||||||
| chr5:75479948
|
C | A | 3 | a0001c0001t0006g0134a0001c0001t0006g0256a0001c0001t0006g0308 | 3 | HG02615.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.232-20767G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75479948 | ||||||
| chr5:75480046
|
AC | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-20866delG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480046 | ||||||
| chr5:75480098
|
C | A | 1 | a0001c0002t0001g0011 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.232-20917G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480098 | ||||||
| chr5:75480164
|
T | G | 84 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(81): Show | 84 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.232-20983A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480164 | ||||||
| chr5:75480295
|
G | C | 5 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-21114C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480295 | ||||||
| chr5:75480525
|
C | T | 13 | a0001c0001t0006g0134a0001c0001t0006g0233a0001c0001t0006g0234others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.232-21344G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480525 | ||||||
| chr5:75480678
|
T | C | 4 | a0001c0002t0001g0089a0001c0002t0001g0094a0001c0002t0001g0095others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-21497A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480678 | ||||||
| chr5:75480734
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.232-21553T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480734 | ||||||
| chr5:75480784
|
C | G | 1 | a0001c0001t0006g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.232-21603G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480784 | ||||||
| chr5:75480876
|
GT | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-21696delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480876 | ||||||
| chr5:75480994
|
C | T | 4 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(1): Show | 4 | NA18612.hp2 NA18979.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-21813G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75480994 | ||||||
| chr5:75481246
|
G | A | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232-22065C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481246 | ||||||
| chr5:75481450
|
G | GT | 7 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-22270dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481450 | ||||||
| chr5:75481528
|
A | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232-22347T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481528 | ||||||
| chr5:75481556
|
C | A | 1 | a0001c0002t0001g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.232-22375G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481556 | ||||||
| chr5:75481580
|
A | G | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.232-22399T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481580 | ||||||
| chr5:75481806
|
C | T | 6 | a0001c0002t0001g0028a0001c0002t0001g0064a0001c0002t0001g0065others(3): Show | 6 | HG02040.hp2 HG03490.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-22625G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481806 | ||||||
| chr5:75481826
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.232-22645T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481826 | ||||||
| chr5:75481836
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232-22655C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75481836 | ||||||
| chr5:75482126
|
C | T | 1 | a0001c0001t0012g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.232-22945G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482126 | ||||||
| chr5:75482180
|
T | C | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.232-22999A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482180 | ||||||
| chr5:75482282
|
T | C | 3 | a0001c0001t0005g0274a0001c0001t0005g0275a0001c0001t0005g0276 | 3 | HG00741.hp2 HG01106.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.232-23101A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482282 | ||||||
| chr5:75482507
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.232-23326T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482507 | ||||||
| chr5:75482570
|
T | C | 2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.232-23389A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482570 | ||||||
| chr5:75482655
|
T | C | 3 | a0001c0001t0002g0223a0001c0001t0002g0252a0001c0001t0017g0253 | 3 | HG01069.hp2 HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.231+23327A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482655 | ||||||
| chr5:75482844
|
C | T | 82 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(79): Show | 82 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.231+23138G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482844 | ||||||
| chr5:75482994
|
T | C | 7 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0093others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+22988A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75482994 | ||||||
| chr5:75483243
|
T | C | 1 | a0001c0002t0001g0020 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.231+22739A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483243 | ||||||
| chr5:75483292
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.231+22690A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483292 | ||||||
| chr5:75483372
|
T | C | 1 | a0001c0001t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.231+22610A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483372 | ||||||
| chr5:75483473
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+22509C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483473 | ||||||
| chr5:75483666
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.231+22316T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483666 | ||||||
| chr5:75483711
|
T | C | 1 | a0001c0001t0002g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.231+22271A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483711 | ||||||
| chr5:75483851
|
A | G | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+22131T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483851 | ||||||
| chr5:75483922
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.231+22060T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483922 | ||||||
| chr5:75483985
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.231+21997G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75483985 | ||||||
| chr5:75484112
|
TTC | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+21868_231+2186 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484112 | ||||||
| chr5:75484142
|
G | A | 8 | a0001c0001t0002g0225a0001c0001t0002g0227a0001c0001t0007g0173others(5): Show | 8 | HG00735.hp2 HG02165.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.231+21840C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484142 | ||||||
| chr5:75484188
|
T | C | 1 | a0001c0001t0002g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.231+21794A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484188 | ||||||
| chr5:75484216
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+21766T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484216 | ||||||
| chr5:75484289
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+21693C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484289 | ||||||
| chr5:75484335
|
A | G | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+21647T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484335 | ||||||
| chr5:75484374
|
T | C | 1 | a0001c0002t0009g0328 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.231+21608A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484374 | ||||||
| chr5:75484443
|
A | G | 1 | a0001c0001t0005g0277 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.231+21539T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484443 | ||||||
| chr5:75484462
|
T | TA | 6 | a0001c0002t0001g0028a0001c0002t0009g0323a0001c0002t0009g0324others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+21519dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484462 | ||||||
| chr5:75484490
|
T | TC | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.231+21491dupG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484490 | ||||||
| chr5:75484513
|
G | A | 14 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(11): Show | 14 | HG01361.hp1 HG01515.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.231+21469C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484513 | ||||||
| chr5:75484606
|
GACA | G | 74 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.231+21373_231+2137 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484606 | ||||||
| chr5:75484622
|
A | C | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+21360T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484622 | ||||||
| chr5:75484815
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.231+21167A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484815 | ||||||
| chr5:75484918
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.231+21064G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484918 | ||||||
| chr5:75484957
|
A | G | 1 | a0001c0001t0003g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.231+21025T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75484957 | ||||||
| chr5:75485312
|
C | CA | 59 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(56): Show | 59 | HG00642.hp1 HG00735.hp1 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.231+20669dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485312 | ||||||
| chr5:75485312
|
C | CAA | 112 | a0001c0001t0001g0036a0001c0001t0003g0132a0001c0001t0003g0180others(109): Show | 112 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.231+20668_231+2066 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485312 | ||||||
| chr5:75485312
|
C | CAAA | 18 | a0001c0001t0005g0271a0001c0001t0006g0308a0001c0002t0001g0013others(15): Show | 18 | HG00438.hp1 HG00741.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.231+20667_231+2066 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485312 | ||||||
| chr5:75485312
|
CA | C | 33 | a0001c0001t0002g0135a0001c0001t0002g0138a0001c0001t0002g0139others(30): Show | 33 | HG00099.hp2 HG00642.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.231+20669delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485312 | ||||||
| chr5:75485312
|
CAA | C | 8 | a0001c0001t0002g0136a0001c0001t0011g0158a0001c0002t0009g0323others(5): Show | 8 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+20668_231+2066 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485312 | ||||||
| chr5:75485312
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.231+20660_231+2066 others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485312 | ||||||
| chr5:75485614
|
G | C | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.231+20368C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485614 | ||||||
| chr5:75485623
|
C | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.231+20359G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485623 | ||||||
| chr5:75485678
|
A | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+20304T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485678 | ||||||
| chr5:75485800
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+20182A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485800 | ||||||
| chr5:75485898
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+20084C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485898 | ||||||
| chr5:75485929
|
G | A | 27 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(24): Show | 27 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.231+20053C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485929 | ||||||
| chr5:75485952
|
A | G | 41 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(38): Show | 41 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.231+20030T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75485952 | ||||||
| chr5:75486008
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+19974G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486008 | ||||||
| chr5:75486300
|
C | T | 127 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(124): Show | 127 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.231+19682G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486300 | ||||||
| chr5:75486586
|
T | G | 1 | a0001c0001t0002g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.231+19396A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486586 | ||||||
| chr5:75486587
|
T | A | 28 | a0001c0001t0003g0131a0001c0001t0003g0172a0001c0001t0003g0175others(25): Show | 28 | HG00642.hp1 HG01192.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.231+19395A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486587 | ||||||
| chr5:75486632
|
T | G | 1 | a0001c0002t0001g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.231+19350A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486632 | ||||||
| chr5:75486735
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+19247C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486735 | ||||||
| chr5:75486814
|
C | A | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.231+19168G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75486814 | ||||||
| chr5:75487212
|
C | G | 1 | a0001c0002t0004g0029 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.231+18770G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487212 | ||||||
| chr5:75487224
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.231+18758A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487224 | ||||||
| chr5:75487358
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+18624C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487358 | ||||||
| chr5:75487379
|
A | G | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+18603T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487379 | ||||||
| chr5:75487406
|
A | C | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.231+18576T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487406 | ||||||
| chr5:75487665
|
A | C | 41 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(38): Show | 41 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.231+18317T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487665 | ||||||
| chr5:75487725
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+18257T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487725 | ||||||
| chr5:75487811
|
C | T | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.231+18171G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487811 | ||||||
| chr5:75487886
|
C | T | 24 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0097others(21): Show | 24 | HG01123.hp2 HG01358.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+18096G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487886 | ||||||
| chr5:75487971
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.231+18011G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75487971 | ||||||
| chr5:75488145
|
AAC | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+17835_231+1783 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488145 | ||||||
| chr5:75488211
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+17771A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488211 | ||||||
| chr5:75488344
|
T | A | 8 | a0001c0002t0004g0060a0001c0002t0004g0061a0001c0002t0009g0323others(5): Show | 8 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+17638A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488344 | ||||||
| chr5:75488345
|
A | T | 3 | a0001c0002t0001g0072a0001c0002t0001g0090a0001c0002t0004g0008 | 3 | HG03486.hp1 NA18957.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.231+17637T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488345 | ||||||
| chr5:75488483
|
T | C | 1 | a0001c0002t0001g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.231+17499A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488483 | ||||||
| chr5:75488514
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+17468A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488514 | ||||||
| chr5:75488917
|
T | G | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.231+17065A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488917 | ||||||
| chr5:75488919
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+17063A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488919 | ||||||
| chr5:75488974
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+17008G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488974 | ||||||
| chr5:75488976
|
T | A | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+17006A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75488976 | ||||||
| chr5:75489220
|
C | T | 1 | a0001c0001t0007g0195 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.231+16762G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75489220 | ||||||
| chr5:75489326
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+16656G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75489326 | ||||||
| chr5:75489415
|
A | T | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 6 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+16567T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75489415 | ||||||
| chr5:75489735
|
A | G | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.231+16247T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75489735 | ||||||
| chr5:75489891
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.231+16091G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75489891 | ||||||
| chr5:75490054
|
G | T | 12 | a0001c0001t0006g0134a0001c0001t0006g0233a0001c0001t0006g0234others(9): Show | 12 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.231+15928C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490054 | ||||||
| chr5:75490104
|
C | T | 1 | a0001c0002t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.231+15878G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490104 | ||||||
| chr5:75490143
|
C | G | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+15839G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490143 | ||||||
| chr5:75490211
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.231+15771C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490211 | ||||||
| chr5:75490258
|
G | A | 163 | a0001c0001t0001g0036a0001c0001t0003g0120a0001c0001t0003g0131others(160): Show | 163 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.231+15724C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490258 | ||||||
| chr5:75490304
|
CCTGCACA others(2): Show |
C | 66 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(63): Show | 66 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.231+15669_231+1567 others(13): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490304 | ||||||
| chr5:75490495
|
TTTTA | T | 5 | a0001c0002t0001g0064a0001c0002t0001g0065a0001c0002t0001g0066others(2): Show | 5 | HG02040.hp2 NA18960.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+15483_231+1548 others(8): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490495 | ||||||
| chr5:75490499
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+15483T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490499 | ||||||
| chr5:75490501
|
TTA | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+15479_231+1548 others(6): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490501 | ||||||
| chr5:75490503
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+15479T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490503 | ||||||
| chr5:75490507
|
A | T | 115 | a0001c0001t0001g0036a0001c0001t0003g0131a0001c0001t0003g0172others(112): Show | 115 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.231+15475T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490507 | ||||||
| chr5:75490507
|
AT | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+15474delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490507 | ||||||
| chr5:75490511
|
T | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0003g0132 | 3 | NA18522.hp1 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.231+15471A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490511 | ||||||
| chr5:75490529
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+15453G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490529 | ||||||
| chr5:75490561
|
C | G | 1 | a0001c0001t0003g0295 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.231+15421G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490561 | ||||||
| chr5:75490568
|
G | A | 5 | a0001c0002t0001g0064a0001c0002t0001g0065a0001c0002t0001g0066others(2): Show | 5 | HG02040.hp2 NA18960.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+15414C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490568 | ||||||
| chr5:75490603
|
C | T | 12 | a0001c0001t0003g0132a0001c0001t0005g0270a0001c0001t0005g0271others(9): Show | 12 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+15379G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490603 | ||||||
| chr5:75490834
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+15148T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490834 | ||||||
| chr5:75490917
|
T | C | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.231+15065A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490917 | ||||||
| chr5:75490933
|
T | G | 33 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(30): Show | 33 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.231+15049A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75490933 | ||||||
| chr5:75491055
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+14927C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491055 | ||||||
| chr5:75491084
|
T | C | 35 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(32): Show | 35 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.231+14898A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491084 | ||||||
| chr5:75491208
|
G | A | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.231+14774C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491208 | ||||||
| chr5:75491217
|
A | C | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+14765T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491217 | ||||||
| chr5:75491353
|
T | G | 1 | a0001c0001t0006g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.231+14629A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491353 | ||||||
| chr5:75491392
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.231+14590T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491392 | ||||||
| chr5:75491485
|
T | C | 247 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(244): Show | 247 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.231+14497A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491485 | ||||||
| chr5:75491541
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.231+14441C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491541 | ||||||
| chr5:75491571
|
C | T | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+14411G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491571 | ||||||
| chr5:75491634
|
G | A | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+14348C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491634 | ||||||
| chr5:75491656
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.231+14326C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491656 | ||||||
| chr5:75491702
|
T | G | 1 | a0001c0007t0001g0336 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.231+14280A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491702 | ||||||
| chr5:75491795
|
G | A | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.231+14187C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75491795 | ||||||
| chr5:75492352
|
G | C | 2 | a0001c0002t0001g0334a0001c0002t0001g0335 | 2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.231+13630C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492352 | ||||||
| chr5:75492442
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+13540C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492442 | ||||||
| chr5:75492475
|
G | T | 1 | a0001c0001t0002g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.231+13507C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492475 | ||||||
| chr5:75492486
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+13496G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492486 | ||||||
| chr5:75492578
|
T | C | 35 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(32): Show | 35 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.231+13404A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492578 | ||||||
| chr5:75492707
|
ATACAG | A | 9 | a0001c0001t0003g0172a0001c0001t0003g0299a0001c0001t0003g0300others(6): Show | 9 | HG00642.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+13270_231+1327 others(9): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492707 | ||||||
| chr5:75492744
|
A | T | 1 | a0001c0007t0001g0336 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.231+13238T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492744 | ||||||
| chr5:75492854
|
T | G | 2 | a0001c0001t0014g0237a0001c0001t0014g0238 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.231+13128A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492854 | ||||||
| chr5:75492902
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+13080C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492902 | ||||||
| chr5:75492905
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.231+13077A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492905 | ||||||
| chr5:75492977
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+13005G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75492977 | ||||||
| chr5:75493225
|
T | G | 1 | a0001c0001t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.231+12757A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75493225 | ||||||
| chr5:75493361
|
AAAC | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+12618_231+1262 others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75493361 | ||||||
| chr5:75493425
|
G | A | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.231+12557C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75493425 | ||||||
| chr5:75493665
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.231+12317G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75493665 | ||||||
| chr5:75494150
|
T | C | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+11832A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494150 | ||||||
| chr5:75494274
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+11708A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494274 | ||||||
| chr5:75494275
|
G | A | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+11707C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494275 | ||||||
| chr5:75494295
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+11687A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494295 | ||||||
| chr5:75494299
|
C | T | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.231+11683G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494299 | ||||||
| chr5:75494415
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+11567A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494415 | ||||||
| chr5:75494456
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+11526C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494456 | ||||||
| chr5:75494503
|
TC | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+11478delG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494503 | ||||||
| chr5:75494867
|
A | G | 1 | a0001c0001t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.231+11115T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75494867 | ||||||
| chr5:75495179
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.231+10803C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495179 | ||||||
| chr5:75495339
|
T | C | 1 | a0001c0001t0003g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.231+10643A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495339 | ||||||
| chr5:75495432
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.231+10550G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495432 | ||||||
| chr5:75495563
|
C | CAAAAAAA others(3): Show |
6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+10409_231+1041 others(14): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495563 | ||||||
| chr5:75495652
|
T | C | 2 | a0001c0001t0002g0190a0001c0001t0002g0239 | 2 | NA18977.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.231+10330A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495652 | ||||||
| chr5:75495804
|
G | C | 1 | a0001c0002t0001g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.231+10178C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495804 | ||||||
| chr5:75495920
|
T | TA | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+10061dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75495920 | ||||||
| chr5:75496000
|
G | C | 1 | a0001c0002t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.231+9982C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496000 | ||||||
| chr5:75496090
|
C | T | 1 | a0001c0001t0006g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.231+9892G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496090 | ||||||
| chr5:75496188
|
A | G | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+9794T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496188 | ||||||
| chr5:75496301
|
A | C | 1 | a0001c0001t0002g0193 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.231+9681T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496301 | ||||||
| chr5:75496369
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+9613C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496369 | ||||||
| chr5:75496428
|
T | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+9554A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496428 | ||||||
| chr5:75496549
|
T | A | 3 | a0001c0001t0012g0240a0001c0001t0012g0241a0001c0002t0001g0248 | 3 | HG02723.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.231+9433A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496549 | ||||||
| chr5:75496748
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.231+9234T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496748 | ||||||
| chr5:75496832
|
G | T | 155 | a0001c0001t0001g0036a0001c0001t0003g0131a0001c0001t0003g0172others(152): Show | 155 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.231+9150C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496832 | ||||||
| chr5:75496868
|
T | C | 3 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071 | 3 | NA19068.hp2 NA19075.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.231+9114A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496868 | ||||||
| chr5:75496996
|
T | C | 1 | a0001c0001t0003g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.231+8986A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496996 | ||||||
| chr5:75496998
|
G | A | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+8984C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75496998 | ||||||
| chr5:75497176
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+8806C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497176 | ||||||
| chr5:75497180
|
C | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+8802G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497180 | ||||||
| chr5:75497184
|
T | A | 1 | a0001c0001t0003g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.231+8798A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497184 | ||||||
| chr5:75497446
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.231+8536C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497446 | ||||||
| chr5:75497686
|
T | C | 149 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(146): Show | 149 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.231+8296A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497686 | ||||||
| chr5:75497944
|
T | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.231+8038A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497944 | ||||||
| chr5:75497982
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+8000T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75497982 | ||||||
| chr5:75498141
|
ATGATTTA others(4978): Show |
A | 1 | a0001c0001t0005g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.231+2856_231+7840d others(2): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498141 | ||||||
| chr5:75498258
|
C | G | 1 | a0001c0002t0001g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.231+7724G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498258 | ||||||
| chr5:75498259
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.231+7723C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498259 | ||||||
| chr5:75498286
|
A | T | 1 | a0001c0007t0001g0336 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.231+7696T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498286 | ||||||
| chr5:75498327
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+7655G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498327 | ||||||
| chr5:75498364
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.231+7618G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498364 | ||||||
| chr5:75498386
|
C | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0025a0001c0002t0001g0026 | 3 | NA18953.hp1 NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.231+7596G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498386 | ||||||
| chr5:75498503
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.231+7479G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498503 | ||||||
| chr5:75498513
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+7469A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498513 | ||||||
| chr5:75498595
|
C | A | 1 | a0001c0001t0003g0295 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.231+7387G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498595 | ||||||
| chr5:75498703
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.231+7279C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498703 | ||||||
| chr5:75498823
|
A | G | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.231+7159T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75498823 | ||||||
| chr5:75499084
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+6898C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499084 | ||||||
| chr5:75499191
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.231+6791C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499191 | ||||||
| chr5:75499327
|
T | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG01516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.231+6655A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499327 | ||||||
| chr5:75499421
|
T | C | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+6561A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499421 | ||||||
| chr5:75499627
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+6355T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499627 | ||||||
| chr5:75499639
|
T | C | 1 | a0001c0001t0002g0005 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.231+6343A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499639 | ||||||
| chr5:75499667
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.231+6315C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499667 | ||||||
| chr5:75499735
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.231+6247G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499735 | ||||||
| chr5:75499856
|
C | T | 74 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.231+6126G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75499856 | ||||||
| chr5:75500062
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+5920T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500062 | ||||||
| chr5:75500080
|
T | G | 5 | a0001c0002t0001g0013a0001c0002t0001g0073a0001c0002t0001g0074others(2): Show | 5 | HG02165.hp2 NA18964.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+5902A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500080 | ||||||
| chr5:75500142
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+5840T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500142 | ||||||
| chr5:75500149
|
G | A | 1 | a0001c0002t0009g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.231+5833C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500149 | ||||||
| chr5:75500190
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.231+5792G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500190 | ||||||
| chr5:75500322
|
G | A | 4 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0011g0158others(1): Show | 4 | NA18968.hp2 NA18992.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+5660C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500322 | ||||||
| chr5:75500382
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.231+5600G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500382 | ||||||
| chr5:75500463
|
G | A | 34 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.231+5519C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500463 | ||||||
| chr5:75500569
|
TAGC | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+5410_231+5412d others(5): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500569 | ||||||
| chr5:75500715
|
A | G | 10 | a0001c0001t0005g0270a0001c0001t0005g0272a0001c0001t0005g0273others(7): Show | 10 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+5267T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500715 | ||||||
| chr5:75500739
|
G | C | 6 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+5243C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500739 | ||||||
| chr5:75500895
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+5087G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500895 | ||||||
| chr5:75500932
|
G | A | 82 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(79): Show | 82 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.231+5050C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500932 | ||||||
| chr5:75500985
|
G | GT | 32 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(29): Show | 32 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+4996dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75500985 | ||||||
| chr5:75501042
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.231+4940C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501042 | ||||||
| chr5:75501137
|
A | G | 1 | a0001c0001t0002g0005 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.231+4845T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501137 | ||||||
| chr5:75501156
|
A | AT | 6 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0021others(3): Show | 6 | HG00438.hp1 HG02015.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+4825dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501156 | ||||||
| chr5:75501185
|
GA | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+4796delT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501185 | ||||||
| chr5:75501210
|
C | G | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+4772G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501210 | ||||||
| chr5:75501280
|
G | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+4702C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501280 | ||||||
| chr5:75501328
|
C | T | 38 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(35): Show | 38 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.231+4654G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501328 | ||||||
| chr5:75501364
|
A | G | 2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.231+4618T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501364 | ||||||
| chr5:75501382
|
G | T | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.231+4600C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501382 | ||||||
| chr5:75501449
|
G | A | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+4533C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501449 | ||||||
| chr5:75501800
|
A | C | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.231+4182T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75501800 | ||||||
| chr5:75502082
|
A | C | 2 | a0001c0001t0002g0188a0001c0001t0015g0004 | 2 | HG00140.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.231+3900T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502082 | ||||||
| chr5:75502240
|
A | G | 7 | a0001c0001t0008g0261a0001c0001t0008g0262a0001c0001t0008g0264others(4): Show | 7 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+3742T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502240 | ||||||
| chr5:75502331
|
G | A | 81 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.231+3651C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502331 | ||||||
| chr5:75502519
|
T | A | 1 | a0001c0002t0001g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.231+3463A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502519 | ||||||
| chr5:75502789
|
T | C | 5 | a0001c0001t0005g0270a0001c0001t0005g0277a0001c0001t0005g0278others(2): Show | 5 | HG01167.hp2 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+3193A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502789 | ||||||
| chr5:75502833
|
A | T | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.231+3149T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502833 | ||||||
| chr5:75502884
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.231+3098C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75502884 | ||||||
| chr5:75503189
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+2793A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503189 | ||||||
| chr5:75503226
|
G | A | 17 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(14): Show | 17 | HG03704.hp2 HG03927.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.231+2756C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503226 | ||||||
| chr5:75503458
|
A | C | 1 | a0001c0001t0002g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.231+2524T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503458 | ||||||
| chr5:75503558
|
G | T | 1 | a0001c0002t0004g0018 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.231+2424C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503558 | ||||||
| chr5:75503612
|
A | G | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+2370T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503612 | ||||||
| chr5:75503658
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.231+2324A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503658 | ||||||
| chr5:75503712
|
C | G | 1 | a0001c0002t0001g0082 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.231+2270G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503712 | ||||||
| chr5:75503713
|
G | A | 1 | a0001c0001t0003g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.231+2269C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503713 | ||||||
| chr5:75503713
|
G | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+2269C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503713 | ||||||
| chr5:75503734
|
A | G | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.231+2248T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503734 | ||||||
| chr5:75503803
|
T | C | 1 | a0001c0001t0008g0266 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.231+2179A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503803 | ||||||
| chr5:75503830
|
A | AATTTAAA others(86): Show |
48 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0138others(45): Show | 48 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.231+2151_231+2152i others(95): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503830 | ||||||
| chr5:75503832
|
T | TTTAAATT others(147): Show |
1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.231+2149_231+2150i others(156): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503832 | ||||||
| chr5:75503863
|
T | TTTAAATT others(116): Show |
1 | a0001c0002t0022g0014 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.231+2118_231+2119i others(125): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503863 | ||||||
| chr5:75503863
|
T | TTTAAATT others(147): Show |
1 | a0001c0001t0002g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.231+2118_231+2119i others(156): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503863 | ||||||
| chr5:75503863
|
T | TTTAAATT others(85): Show |
2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.231+2118_231+2119i others(94): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503863 | ||||||
| chr5:75503863
|
T | TTTAAATT others(116): Show |
29 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0091others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.231+2118_231+2119i others(125): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503863 | ||||||
| chr5:75503863
|
T | TTTAAATT others(147): Show |
1 | a0001c0002t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.231+2118_231+2119i others(156): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503863 | ||||||
| chr5:75503870
|
T | TAAATG | 231 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(228): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.231+2111_231+2112i others(7): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503870 | ||||||
| chr5:75503871
|
T | A | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.231+2111A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503871 | ||||||
| chr5:75503872
|
T | A | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.231+2110A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503872 | ||||||
| chr5:75503873
|
T | A | 1 | a0001c0002t0019g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.231+2109A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAAATTTA others(143): Show |
1 | a0001c0002t0021g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.231+2108_231+2109i others(152): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(49): Show |
1 | a0001c0001t0002g0250 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.231+2108_231+2109i others(58): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(173): Show |
1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.231+2108_231+2109i others(182): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(261): Show |
2 | a0001c0001t0003g0297a0001c0001t0003g0298 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(270): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(142): Show |
74 | a0001c0001t0001g0036a0001c0001t0015g0004a0001c0002t0001g0009others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(151): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(173): Show |
3 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0335 | 3 | HG01884.hp2 NA18941.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(182): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(173): Show |
3 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0002t0001g0078 | 3 | HG00438.hp2 HG01069.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(182): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(204): Show |
1 | a0001c0001t0017g0253 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(213): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(172): Show |
1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(181): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(142): Show |
4 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(1): Show | 4 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(151): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(173): Show |
1 | a0001c0002t0001g0086 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(182): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(155): Show |
1 | a0001c0001t0007g0173 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.231+2108_231+2109i others(164): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(173): Show |
96 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(182): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(204): Show |
2 | a0001c0001t0002g0130a0002c0003t0002g0129 | 2 | NA18991.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(213): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(217): Show |
9 | a0001c0001t0003g0172a0001c0001t0003g0299a0001c0001t0003g0300others(6): Show | 9 | HG00642.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(226): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(235): Show |
2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(244): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(230): Show |
1 | a0001c0001t0003g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.231+2108_231+2109i others(239): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(204): Show |
5 | a0001c0001t0001g0321a0001c0001t0003g0287a0001c0001t0003g0288others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(213): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(199): Show |
2 | a0001c0001t0005g0270a0001c0001t0005g0271 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(208): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(230): Show |
2 | a0001c0001t0003g0294a0001c0001t0003g0295 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(239): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(204): Show |
11 | a0001c0001t0002g0185a0001c0001t0005g0272a0001c0001t0005g0273others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(213): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(230): Show |
1 | a0001c0001t0003g0293 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(239): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TAATTTAA others(235): Show |
7 | a0001c0001t0003g0131a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(244): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TTGTTTAA others(178): Show |
1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(187): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TTGTTTAA others(116): Show |
1 | a0001c0002t0018g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(125): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TTGTTTAA others(209): Show |
2 | a0001c0001t0003g0291a0001c0001t0003g0292 | 2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.231+2108_231+2109i others(218): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TTGTTTAA others(178): Show |
10 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(7): Show | 10 | HG01071.hp2 HG01192.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+2108_231+2109i others(187): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75503873
|
T | TTGTTTAA others(178): Show |
1 | a0001c0001t0002g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.231+2108_231+2109i others(187): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75503873 | ||||||
| chr5:75504055
|
A | C | 1 | a0001c0002t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.231+1927T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504055 | ||||||
| chr5:75504147
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+1835C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504147 | ||||||
| chr5:75504409
|
T | C | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.231+1573A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504409 | ||||||
| chr5:75504414
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+1568A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504414 | ||||||
| chr5:75504585
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+1397A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504585 | ||||||
| chr5:75504586
|
A | G | 1 | a0001c0001t0002g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.231+1396T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504586 | ||||||
| chr5:75504656
|
ACT | A | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+1324_231+1325d others(4): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504656 | ||||||
| chr5:75504705
|
A | C | 1 | a0001c0001t0006g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.231+1277T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504705 | ||||||
| chr5:75504706
|
G | C | 1 | a0001c0001t0006g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.231+1276C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504706 | ||||||
| chr5:75504751
|
CT | C | 112 | a0001c0001t0001g0036a0001c0001t0002g0257a0001c0001t0013g0258others(109): Show | 112 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.231+1230delA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504751 | ||||||
| chr5:75504919
|
T | C | 1 | a0001c0002t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1063A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504919 | ||||||
| chr5:75504932
|
ATTCATGT others(8): Show |
A | 1 | a0001c0001t0002g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.231+1035_231+1049d others(17): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504932 | ||||||
| chr5:75504955
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.231+1027C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75504955 | ||||||
| chr5:75505001
|
A | C | 1 | a0001c0001t0006g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.231+981T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505001 | ||||||
| chr5:75505055
|
G | C | 1 | a0001c0002t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.231+927C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505055 | ||||||
| chr5:75505148
|
G | A | 1 | a0001c0002t0009g0324 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.231+834C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505148 | ||||||
| chr5:75505285
|
AAAAACAA others(8): Show |
A | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG02559.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+682_231+696del others(15): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505285 | ||||||
| chr5:75505389
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.231+593A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505389 | ||||||
| chr5:75505392
|
G | C | 6 | a0001c0001t0003g0293a0001c0001t0003g0294a0001c0001t0003g0295others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+590C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505392 | ||||||
| chr5:75505445
|
G | A | 8 | a0001c0001t0002g0265a0001c0001t0008g0261a0001c0001t0008g0262others(5): Show | 8 | HG01515.hp2 HG01975.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.231+537C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505445 | ||||||
| chr5:75505459
|
A | T | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.231+523T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505459 | ||||||
| chr5:75505540
|
A | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+442T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505540 | ||||||
| chr5:75505579
|
T | G | 2 | a0001c0001t0008g0267a0001c0001t0008g0309 | 2 | HG01981.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.231+403A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505579 | ||||||
| chr5:75505581
|
G | A | 1 | a0001c0002t0020g0007 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.231+401C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505581 | ||||||
| chr5:75505599
|
T | G | 1 | a0001c0002t0004g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.231+383A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505599 | ||||||
| chr5:75505751
|
A | G | 1 | a0001c0002t0001g0009 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.231+231T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505751 | ||||||
| chr5:75505911
|
C | T | 10 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(7): Show | 10 | NA18942.hp1 NA18974.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.231+71G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 2/16 | chr5 | 75505911 | ||||||
| chr5:75506491
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.97-375A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75506491 | ||||||
| chr5:75506623
|
T | A | 11 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-507A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75506623 | ||||||
| chr5:75506647
|
A | T | 1 | a0001c0001t0002g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.97-531T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75506647 | ||||||
| chr5:75506814
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.97-698G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75506814 | ||||||
| chr5:75506833
|
T | C | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.97-717A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75506833 | ||||||
| chr5:75506880
|
T | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG01255.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.97-764A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75506880 | ||||||
| chr5:75507200
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-1084A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75507200 | ||||||
| chr5:75507429
|
C | G | 1 | a0001c0001t0003g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.97-1313G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75507429 | ||||||
| chr5:75507442
|
C | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-1326G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75507442 | ||||||
| chr5:75507588
|
C | G | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-1472G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75507588 | ||||||
| chr5:75507790
|
C | T | 332 | a0001c0001t0001g0036a0001c0001t0001g0310a0001c0001t0001g0311others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.97-1674G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75507790 | ||||||
| chr5:75507896
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-1780A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75507896 | ||||||
| chr5:75508069
|
C | T | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.97-1953G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508069 | ||||||
| chr5:75508228
|
G | GT | 10 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(7): Show | 10 | NA18942.hp1 NA18974.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-2113dupA | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508228 | ||||||
| chr5:75508277
|
GTT | G | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.97-2163_97-2162del others(2): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508277 | ||||||
| chr5:75508330
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-2214C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508330 | ||||||
| chr5:75508332
|
A | T | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-2216T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508332 | ||||||
| chr5:75508348
|
T | C | 13 | a0001c0001t0003g0120a0001c0001t0003g0287a0001c0001t0003g0288others(10): Show | 13 | HG01081.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-2232A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508348 | ||||||
| chr5:75508634
|
A | C | 1 | a0001c0002t0004g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+2478T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508634 | ||||||
| chr5:75508817
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.96+2295T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508817 | ||||||
| chr5:75508901
|
G | T | 2 | a0001c0002t0019g0006a0001c0002t0020g0007 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.96+2211C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75508901 | ||||||
| chr5:75509163
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.96+1949T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509163 | ||||||
| chr5:75509503
|
C | A | 7 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+1609G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509503 | ||||||
| chr5:75509554
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1558C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509554 | ||||||
| chr5:75509557
|
T | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1555A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509557 | ||||||
| chr5:75509559
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1553G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509559 | ||||||
| chr5:75509562
|
T | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1550A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509562 | ||||||
| chr5:75509563
|
TTTTTTAT others(3): Show |
T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1539_96+1548del others(10): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509563 | ||||||
| chr5:75509576
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1536C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509576 | ||||||
| chr5:75509580
|
A | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1532T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509580 | ||||||
| chr5:75509585
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1527G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509585 | ||||||
| chr5:75509586
|
T | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1526A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509586 | ||||||
| chr5:75509590
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1522C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509590 | ||||||
| chr5:75509592
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1520C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509592 | ||||||
| chr5:75509593
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1519G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509593 | ||||||
| chr5:75509598
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1514C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509598 | ||||||
| chr5:75509602
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1510G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509602 | ||||||
| chr5:75509605
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1507A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509605 | ||||||
| chr5:75509607
|
T | TC | 8 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(5): Show | 8 | HG00642.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1504dupG | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509607 | ||||||
| chr5:75509609
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1503G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509609 | ||||||
| chr5:75509610
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1502G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509610 | ||||||
| chr5:75509612
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1500G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509612 | ||||||
| chr5:75509613
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1499C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509613 | ||||||
| chr5:75509614
|
G | GAAAAGAG others(8): Show |
1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1497_96+1498ins others(15): Show |
CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509614 | ||||||
| chr5:75509615
|
T | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1497A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509615 | ||||||
| chr5:75509616
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1496G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509616 | ||||||
| chr5:75509618
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1494G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509618 | ||||||
| chr5:75509621
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1491G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509621 | ||||||
| chr5:75509622
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1490T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509622 | ||||||
| chr5:75509625
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1487G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509625 | ||||||
| chr5:75509627
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1485G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509627 | ||||||
| chr5:75509628
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1484G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509628 | ||||||
| chr5:75509630
|
A | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1482T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509630 | ||||||
| chr5:75509632
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1480G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509632 | ||||||
| chr5:75509633
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1479G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509633 | ||||||
| chr5:75509634
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1478G>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509634 | ||||||
| chr5:75509636
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1476G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509636 | ||||||
| chr5:75509637
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1475T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509637 | ||||||
| chr5:75509640
|
A | C | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1472T>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509640 | ||||||
| chr5:75509646
|
A | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1466T>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509646 | ||||||
| chr5:75509647
|
T | G | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1465A>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509647 | ||||||
| chr5:75509648
|
T | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1464A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509648 | ||||||
| chr5:75509650
|
T | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1462A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509650 | ||||||
| chr5:75509653
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1459C>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509653 | ||||||
| chr5:75509656
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1456C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509656 | ||||||
| chr5:75509657
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1455C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509657 | ||||||
| chr5:75509658
|
T | A | 1 | a0001c0001t0002g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.96+1454A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509658 | ||||||
| chr5:75509798
|
T | A | 1 | a0001c0001t0006g0308 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.96+1314A>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509798 | ||||||
| chr5:75509825
|
T | C | 1 | a0001c0001t0008g0309 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.96+1287A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75509825 | ||||||
| chr5:75510022
|
T | C | 13 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(10): Show | 13 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+1090A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510022 | ||||||
| chr5:75510222
|
T | TA | 32 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0090others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.96+889dupT | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510222 | ||||||
| chr5:75510279
|
C | T | 127 | a0001c0001t0001g0036a0001c0002t0001g0009a0001c0002t0001g0010others(124): Show | 127 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.96+833G>A | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510279 | ||||||
| chr5:75510535
|
A | G | 1 | a0001c0001t0002g0005 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.96+577T>C | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510535 | ||||||
| chr5:75510536
|
T | C | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+576A>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510536 | ||||||
| chr5:75510537
|
G | A | 6 | a0001c0002t0009g0323a0001c0002t0009g0324a0001c0002t0009g0325others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+575C>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510537 | ||||||
| chr5:75510564
|
C | A | 4 | a0001c0002t0009g0325a0001c0002t0009g0326a0001c0002t0009g0327others(1): Show | 4 | HG02132.hp1 HG02135.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+548G>T | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75510564 | ||||||
| chr5:75511063
|
G | C | 7 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+49C>G | CERT1 | ENSG00000113163.19 | transcript | ENST00000643780.2 | protein_coding | 1/16 | chr5 | 75511063 |