Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55756 |
|---|---|
| ensemblid | ENSG00000104299.15 |
| hgncid | 25592 |
| symbol | INTS9 |
| name | integrator complex subunit 9 |
| refseq_nuc | NM_018250.4 |
| refseq_prot | NP_060720.2 |
| ensembl_nuc | ENST00000521022.6 |
| ensembl_prot | ENSP00000429065.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28767661 |
| end | 28889969 |
| strand | - |
| ver | v1.2 |
| region | chr8:28767661-28889969 |
| region5000 | chr8:28762661-28894969 |
| regionname0 | INTS9_chr8_28767661_28889969 |
| regionname5000 | INTS9_chr8_28762661_28894969 |
| 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 | 658 | 355 | 90 | 62 | 153 | 12 | 36 | 125 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0002 | 0/0 | 658 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0003 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0004 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| 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 | 1977 | 344 | 82 | 61 | 152 | 11 | 36 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0002 | 0/0 | 1977 | 4 | 4 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0003 | 0/0 | 1977 | 3 | 2 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0004 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0005 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0006 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0007 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0008 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0009 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| c0010 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 573 | 325 | 63 | 60 | 153 | 12 | 35 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0002 | 0/0 | 573 | 12 | 9 | 2 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0003 | 0/0 | 573 | 8 | 8 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0004 | 0/0 | 573 | 8 | 8 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0005 | 0/0 | 573 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0006 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0007 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| t0008 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| 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 | 2 | 0 | 1 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| 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 | 1977 | 344 | 82 | 61 | 152 | 11 | 36 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0002 | 0/0 | 1977 | 4 | 4 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0003 | 0/0 | 1977 | 3 | 2 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0005 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0007 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0009 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0010 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0002c0006 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0003c0008 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0004c0004 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2549 | 317 | 59 | 59 | 151 | 11 | 35 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0002 | 0/0 | 2549 | 11 | 8 | 2 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0003 | 0/0 | 2549 | 3 | 3 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0004 | 0/0 | 2549 | 8 | 8 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0005 | 0/0 | 2549 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0006 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0007 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0001t0008 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0002t0003 | 0/0 | 2549 | 4 | 4 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0003t0001 | 0/0 | 2549 | 3 | 2 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0005t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0007t0001 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0009t0001 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0001c0010t0003 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0002c0006t0001 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0003c0008t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| a0004c0004t0002 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | copy fasta | chr8 | 28762661 | 28894969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0005t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0007t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0009t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0010t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0002c0006t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0003c0008t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0004c0004t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0009 | t0001 | g0207 | EUR | GBR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00621 | hp2 | a0001 | c0007 | t0001 | g0168 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0136 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02055 | hp1 | a0001 | c0010 | t0003 | g0348 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CDX | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0316 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0194 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02809 | hp2 | a0004 | c0004 | t0002 | g0315 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0295 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02965 | hp2 | a0003 | c0008 | t0001 | g0006 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0297 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0296 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0351 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19079 | hp2 | a0002 | c0006 | t0001 | g0325 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ASW | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0294 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0293 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | USA | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | USA | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0122 | REF | REF | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28769966
|
C | T | 1 | a0002 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.1723G>A | p.Val575Ile | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/17 | 1810/2549 | 1723/1977 | 575/658 | chr8 | 28769966 | ||
| chr8:28813551
|
T | C | 1 | a0003 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.550A>G | p.Met184Val | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/17 | 637/2549 | 550/1977 | 184/658 | chr8 | 28813551 | ||
| chr8:28837641
|
C | T | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.397G>A | p.Gly133Ser | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/17 | 484/2549 | 397/1977 | 133/658 | chr8 | 28837641 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28780908
|
G | A | 1 | a0001c0002 | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.1185C>T | p.Thr395Thr | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/17 | 1272/2549 | 1185/1977 | 395/658 | chr8 | 28780908 | ||
| chr8:28780938
|
G | A | 1 | a0001c0007 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1155C>T | p.Asn385Asn | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/17 | 1242/2549 | 1155/1977 | 385/658 | chr8 | 28780938 | ||
| chr8:28780986
|
C | T | 1 | a0001c0003 | 3 | HG01261.hp1 HG02451.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1107G>A | p.Gln369Gln | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/17 | 1194/2549 | 1107/1977 | 369/658 | chr8 | 28780986 | ||
| chr8:28813588
|
A | G | 1 | a0001c0005 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.513T>C | p.Asp171Asp | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/17 | 600/2549 | 513/1977 | 171/658 | chr8 | 28813588 | ||
| chr8:28850222
|
G | A | 1 | a0001c0009 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.189C>T | p.Phe63Phe | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/17 | 276/2549 | 189/1977 | 63/658 | chr8 | 28850222 | ||
| chr8:28850264
|
C | A | 1 | a0001c0010 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.147G>T | p.Leu49Leu | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/17 | 234/2549 | 147/1977 | 49/658 | chr8 | 28850264 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28767912
|
A | G | 1 | a0001c0001t0006 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 234 | chr8 | 28767912 | |||||
| chr8:28767923
|
G | A | 1 | a0001c0001t0005 | 2 | HG03516.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*223C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 223 | chr8 | 28767923 | |||||
| chr8:28767939
|
G | T | 3 | a0001c0001t0003a0001c0002t0003a0001c0010t0003 | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 207 | chr8 | 28767939 | |||||
| chr8:28768016
|
T | C | 1 | a0001c0001t0004 | 8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*130A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 130 | chr8 | 28768016 | |||||
| chr8:28768070
|
G | C | 4 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(1): Show | 15 | HG00738.hp2 HG01243.hp2 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 76 | chr8 | 28768070 | |||||
| chr8:28768091
|
G | A | 1 | a0001c0001t0007 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 55 | chr8 | 28768091 | |||||
| chr8:28768123
|
G | C | 1 | a0001c0001t0008 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 23 | chr8 | 28768123 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28768594
|
A | C | 1 | a0001c0001t0008g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1801-272T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768594 | ||||||
| chr8:28768625
|
C | T | 1 | a0001c0001t0006g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1801-303G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768625 | ||||||
| chr8:28768738
|
G | A | 4 | a0001c0001t0002g0028a0001c0001t0002g0164a0001c0001t0002g0165others(1): Show | 4 | HG00738.hp2 HG01243.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1801-416C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768738 | ||||||
| chr8:28768819
|
A | G | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1801-497T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768819 | ||||||
| chr8:28768901
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(123): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1801-579G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768901 | ||||||
| chr8:28768953
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 126 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1801-631C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768953 | ||||||
| chr8:28769035
|
T | A | 15 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0314others(12): Show | 16 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1801-713A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769035 | ||||||
| chr8:28769116
|
C | T | 7 | a0001c0001t0002g0146a0001c0001t0002g0274a0001c0001t0002g0312others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1800+773G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769116 | ||||||
| chr8:28769178
|
A | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0104others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1800+711T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769178 | ||||||
| chr8:28769189
|
C | T | 27 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0104others(24): Show | 27 | HG00738.hp2 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1800+700G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769189 | ||||||
| chr8:28769397
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1800+492A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769397 | ||||||
| chr8:28769582
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1800+307G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769582 | ||||||
| chr8:28770195
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-169T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770195 | ||||||
| chr8:28770202
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1663-176G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770202 | ||||||
| chr8:28770279
|
A | G | 7 | a0001c0001t0004g0002a0001c0001t0004g0111a0001c0001t0004g0153others(4): Show | 8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663-253T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770279 | ||||||
| chr8:28770307
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | NA18947.hp1 NA19007.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-281C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770307 | ||||||
| chr8:28770324
|
G | C | 15 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0185others(12): Show | 15 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1663-298C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770324 | ||||||
| chr8:28770350
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-324G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770350 | ||||||
| chr8:28770457
|
T | C | 3 | a0001c0001t0002g0028a0001c0001t0002g0262a0001c0001t0002g0305 | 3 | HG02630.hp2 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1663-431A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770457 | ||||||
| chr8:28770476
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1663-450G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770476 | ||||||
| chr8:28770477
|
G | A | 33 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(30): Show | 33 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1663-451C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770477 | ||||||
| chr8:28770515
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1662+467C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770515 | ||||||
| chr8:28770524
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+458C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770524 | ||||||
| chr8:28770651
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+331T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770651 | ||||||
| chr8:28770659
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1662+323C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770659 | ||||||
| chr8:28770701
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1662+281G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770701 | ||||||
| chr8:28770720
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1662+262G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770720 | ||||||
| chr8:28770767
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1662+215G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770767 | ||||||
| chr8:28770776
|
G | A | 33 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(30): Show | 33 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1662+206C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770776 | ||||||
| chr8:28770881
|
A | G | 8 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0314others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+101T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770881 | ||||||
| chr8:28770903
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(193): Show | 199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1662+79T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770903 | ||||||
| chr8:28771320
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1564-240C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771320 | ||||||
| chr8:28771323
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1564-243G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771323 | ||||||
| chr8:28771324
|
G | A | 2 | a0001c0001t0002g0262a0001c0001t0002g0305 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1564-244C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771324 | ||||||
| chr8:28771636
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1564-556A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771636 | ||||||
| chr8:28771643
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(143): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1564-563C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771643 | ||||||
| chr8:28771656
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1564-576G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771656 | ||||||
| chr8:28771680
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1564-600C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771680 | ||||||
| chr8:28771693
|
G | A | 8 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0314others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564-613C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771693 | ||||||
| chr8:28771699
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1564-619G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771699 | ||||||
| chr8:28771862
|
G | A | 2 | a0001c0001t0002g0262a0001c0001t0002g0305 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1564-782C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771862 | ||||||
| chr8:28771901
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1564-821G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771901 | ||||||
| chr8:28772001
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1564-921G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772001 | ||||||
| chr8:28772234
|
G | A | 32 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(29): Show | 32 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1564-1154C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772234 | ||||||
| chr8:28772239
|
G | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(159): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1564-1159C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772239 | ||||||
| chr8:28772253
|
G | A | 30 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 30 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1564-1173C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772253 | ||||||
| chr8:28772262
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-1182G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772262 | ||||||
| chr8:28772317
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1564-1237G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772317 | ||||||
| chr8:28772407
|
G | A | 1 | a0001c0002t0003g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-1327C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772407 | ||||||
| chr8:28772530
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1564-1450G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772530 | ||||||
| chr8:28772537
|
G | A | 1 | a0001c0002t0003g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1564-1457C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772537 | ||||||
| chr8:28772632
|
CCT | C | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0288others(1): Show | 4 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564-1554_1564-155 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772632 | ||||||
| chr8:28772794
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG00642.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1564-1714C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772794 | ||||||
| chr8:28772801
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02922.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1564-1721G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772801 | ||||||
| chr8:28772806
|
CAAAAAAA others(3): Show |
C | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(123): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1564-1736_1564-172 others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772806 | ||||||
| chr8:28772806
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0263 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1564-1737_1564-172 others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772806 | ||||||
| chr8:28772862
|
A | G | 7 | a0001c0001t0004g0002a0001c0001t0004g0111a0001c0001t0004g0153others(4): Show | 8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564-1782T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772862 | ||||||
| chr8:28773058
|
T | C | 13 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0203others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1564-1978A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773058 | ||||||
| chr8:28773132
|
G | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0273 | 2 | NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1564-2052C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773132 | ||||||
| chr8:28773184
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1564-2104G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773184 | ||||||
| chr8:28773238
|
T | C | 8 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG00597.hp1 HG02027.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-2158A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773238 | ||||||
| chr8:28773274
|
T | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1564-2194A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773274 | ||||||
| chr8:28773279
|
C | T | 15 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 15 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1564-2199G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773279 | ||||||
| chr8:28773371
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1564-2291C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773371 | ||||||
| chr8:28773395
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0222 | 4 | HG02818.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564-2315G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773395 | ||||||
| chr8:28773463
|
C | CA | 8 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0004g0002others(5): Show | 9 | HG02630.hp1 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1563+2295dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | ||||||
| chr8:28773463
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1563+2295delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | ||||||
| chr8:28773463
|
CAA | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(120): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1563+2294_1563+229 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | ||||||
| chr8:28773463
|
CAAA | C | 10 | a0001c0001t0001g0221a0001c0001t0001g0281a0001c0001t0002g0146others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1563+2293_1563+229 others(7): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | ||||||
| chr8:28773464
|
A | C | 1 | a0001c0002t0003g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1563+2295T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773464 | ||||||
| chr8:28773490
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1563+2269T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773490 | ||||||
| chr8:28773554
|
C | CT | 22 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0103others(19): Show | 22 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1563+2204dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773554 | ||||||
| chr8:28773598
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1563+2161G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773598 | ||||||
| chr8:28773664
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1563+2095G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773664 | ||||||
| chr8:28773694
|
G | GT | 141 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(138): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1563+2064dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773694 | ||||||
| chr8:28773694
|
G | GTTT | 8 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0314others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563+2062_1563+206 others(7): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773694 | ||||||
| chr8:28773771
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1563+1988C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773771 | ||||||
| chr8:28773845
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0022 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1563+1914G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773845 | ||||||
| chr8:28773966
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1563+1793G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773966 | ||||||
| chr8:28774016
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1563+1743G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774016 | ||||||
| chr8:28774074
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 135 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.1563+1685G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774074 | ||||||
| chr8:28774093
|
G | A | 2 | a0001c0001t0003g0314a0001c0010t0003g0348 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1563+1666C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774093 | ||||||
| chr8:28774111
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1563+1648G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774111 | ||||||
| chr8:28774298
|
A | G | 8 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0314others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563+1461T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774298 | ||||||
| chr8:28774524
|
GAA | G | 7 | a0001c0001t0004g0002a0001c0001t0004g0111a0001c0001t0004g0153others(4): Show | 8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563+1233_1563+123 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774524 | ||||||
| chr8:28774689
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1563+1070C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774689 | ||||||
| chr8:28775035
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563+724G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775035 | ||||||
| chr8:28775251
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1563+508G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775251 | ||||||
| chr8:28775428
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1563+331G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775428 | ||||||
| chr8:28775462
|
A | G | 13 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+297T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775462 | ||||||
| chr8:28775581
|
A | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1563+178T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775581 | ||||||
| chr8:28775631
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1563+128G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775631 | ||||||
| chr8:28775646
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0288others(1): Show | 4 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1563+113C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775646 | ||||||
| chr8:28775695
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1563+64A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775695 | ||||||
| chr8:28776029
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1396-103T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776029 | ||||||
| chr8:28776071
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1396-145T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776071 | ||||||
| chr8:28776168
|
C | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 124 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1396-242G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776168 | ||||||
| chr8:28776227
|
T | G | 4 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0314others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-301A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776227 | ||||||
| chr8:28776413
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(130): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1396-487C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776413 | ||||||
| chr8:28776427
|
G | GT | 53 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0054others(50): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1396-502dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776427 | ||||||
| chr8:28776427
|
G | GTT | 18 | a0001c0001t0001g0082a0001c0001t0001g0128a0001c0001t0001g0133others(15): Show | 18 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1396-503_1396-502d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776427 | ||||||
| chr8:28776429
|
TTTTTTTT others(4): Show |
T | 12 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(9): Show | 13 | HG00738.hp2 HG01243.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1396-514_1396-504d others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776429 | ||||||
| chr8:28776433
|
TTTTTTTG | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0147others(68): Show | 72 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1396-514_1396-508d others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776433 | ||||||
| chr8:28776436
|
T | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 124 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1396-510A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776436 | ||||||
| chr8:28776438
|
TTG | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 118 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1396-514_1396-513d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776438 | ||||||
| chr8:28776439
|
TG | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0181a0001c0001t0003g0309others(3): Show | 6 | HG02055.hp1 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-514delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776439 | ||||||
| chr8:28776440
|
G | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0054others(74): Show | 78 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1396-514C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776440 | ||||||
| chr8:28776445
|
T | G | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1396-519A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776445 | ||||||
| chr8:28777057
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395+772G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777057 | ||||||
| chr8:28777077
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1395+752A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777077 | ||||||
| chr8:28777259
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1395+570C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777259 | ||||||
| chr8:28777283
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1395+546G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777283 | ||||||
| chr8:28777284
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0228 | 2 | NA18944.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1395+545C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777284 | ||||||
| chr8:28777313
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395+516G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777313 | ||||||
| chr8:28777336
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1395+493G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777336 | ||||||
| chr8:28777338
|
C | T | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1395+491G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777338 | ||||||
| chr8:28777370
|
T | A | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1395+459A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777370 | ||||||
| chr8:28777453
|
T | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0156a0001c0003t0001g0316others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+376A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777453 | ||||||
| chr8:28777540
|
C | CT | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(155): Show | 161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1395+288dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777540 | ||||||
| chr8:28777639
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1395+190C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777639 | ||||||
| chr8:28777680
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1395+149C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777680 | ||||||
| chr8:28777786
|
G | C | 19 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0203others(16): Show | 20 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395+43C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777786 | ||||||
| chr8:28778045
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0287 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1271-92T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778045 | ||||||
| chr8:28778199
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1271-246C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778199 | ||||||
| chr8:28778270
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0067others(50): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1271-317C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778270 | ||||||
| chr8:28778294
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1271-341T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778294 | ||||||
| chr8:28778353
|
G | C | 1 | a0001c0002t0003g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1271-400C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778353 | ||||||
| chr8:28778454
|
G | A | 5 | a0001c0001t0002g0146a0001c0001t0002g0274a0001c0001t0002g0312others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-501C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778454 | ||||||
| chr8:28778592
|
CG | C | 5 | a0001c0001t0002g0146a0001c0001t0002g0274a0001c0001t0002g0312others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-640delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778592 | ||||||
| chr8:28778595
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1271-642C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778595 | ||||||
| chr8:28778730
|
T | C | 5 | a0001c0001t0002g0146a0001c0001t0002g0274a0001c0001t0002g0312others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-777A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778730 | ||||||
| chr8:28778759
|
G | A | 2 | a0001c0001t0002g0274a0004c0004t0002g0315 | 2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1271-806C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778759 | ||||||
| chr8:28778771
|
T | C | 7 | a0001c0001t0004g0002a0001c0001t0004g0111a0001c0001t0004g0153others(4): Show | 8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1271-818A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778771 | ||||||
| chr8:28779078
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1271-1125A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779078 | ||||||
| chr8:28779165
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1271-1212C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779165 | ||||||
| chr8:28779166
|
C | A | 1 | a0001c0001t0001g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1271-1213G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779166 | ||||||
| chr8:28779452
|
T | G | 2 | a0001c0001t0001g0352a0001c0003t0001g0136 | 2 | HG01261.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1270+1371A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779452 | ||||||
| chr8:28779510
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1270+1313A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779510 | ||||||
| chr8:28779639
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0343 | 2 | HG01168.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1270+1184C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779639 | ||||||
| chr8:28779669
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0148a0001c0005t0001g0293 | 3 | HG02258.hp2 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1270+1154G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779669 | ||||||
| chr8:28779818
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG01884.hp1 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1270+1005T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779818 | ||||||
| chr8:28779887
|
C | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1270+936G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779887 | ||||||
| chr8:28780008
|
G | A | 2 | a0001c0001t0001g0345a0001c0001t0001g0352 | 2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1270+815C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780008 | ||||||
| chr8:28780044
|
C | A | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270+779G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780044 | ||||||
| chr8:28780051
|
A | AT | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1270+771_1270+772i others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780051 | ||||||
| chr8:28780052
|
G | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(138): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1270+771C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780052 | ||||||
| chr8:28780053
|
G | GTT | 7 | a0001c0001t0001g0033a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG00639.hp1 HG01069.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1270+768_1270+769d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780053 | ||||||
| chr8:28780053
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1270+770C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780053 | ||||||
| chr8:28780065
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1270+758A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780065 | ||||||
| chr8:28780069
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1270+754G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780069 | ||||||
| chr8:28780070
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1270+753A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780070 | ||||||
| chr8:28780076
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1270+747G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780076 | ||||||
| chr8:28780127
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1270+696G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780127 | ||||||
| chr8:28780129
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1270+694T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780129 | ||||||
| chr8:28780166
|
GGAA | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1270+654_1270+656d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780166 | ||||||
| chr8:28780167
|
G | T | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1270+656C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780167 | ||||||
| chr8:28780178
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0286 | 2 | NA18999.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1270+645T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780178 | ||||||
| chr8:28780227
|
TA | T | 24 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 24 | HG00408.hp1 HG00621.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+595delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAA | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0052others(28): Show | 31 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1270+594_1270+595d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAA | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0102others(24): Show | 28 | HG00597.hp1 HG01109.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.1270+593_1270+595d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAA | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0104others(12): Show | 15 | HG01070.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1270+592_1270+595d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(2): Show |
T | 18 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0032others(15): Show | 18 | HG00735.hp2 HG01175.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270+587_1270+595d others(11): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(3): Show |
T | 79 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 80 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1270+586_1270+595d others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(4): Show |
T | 11 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0156others(8): Show | 12 | HG01069.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1270+585_1270+595d others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+584_1270+595d others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(6): Show |
T | 25 | a0001c0001t0001g0074a0001c0001t0001g0082a0001c0001t0001g0152others(22): Show | 25 | HG00597.hp2 HG00738.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1270+583_1270+595d others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(7): Show |
T | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(96): Show | 101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1270+582_1270+595d others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0270a0001c0001t0001g0276a0001c0001t0001g0302 | 3 | HG01496.hp1 HG01943.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1270+581_1270+595d others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780227
|
TAAAAAAA others(16): Show |
T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0009t0001g0207 | 3 | HG00140.hp1 HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1270+573_1270+595d others(25): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | ||||||
| chr8:28780237
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1270+586T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780237 | ||||||
| chr8:28780341
|
C | T | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270+482G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780341 | ||||||
| chr8:28780356
|
A | G | 3 | a0001c0001t0002g0146a0001c0001t0002g0274a0004c0004t0002g0315 | 3 | HG02809.hp2 HG02965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1270+467T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780356 | ||||||
| chr8:28780361
|
A | G | 1 | a0001c0001t0001g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1270+462T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780361 | ||||||
| chr8:28780515
|
C | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1270+308G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780515 | ||||||
| chr8:28780554
|
G | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1270+269C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780554 | ||||||
| chr8:28780608
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1270+215G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780608 | ||||||
| chr8:28780644
|
A | G | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1270+179T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780644 | ||||||
| chr8:28780664
|
C | A | 6 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(3): Show | 6 | HG00738.hp2 HG01243.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270+159G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780664 | ||||||
| chr8:28780706
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1270+117G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780706 | ||||||
| chr8:28780752
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1270+71A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780752 | ||||||
| chr8:28780796
|
A | G | 9 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0111others(6): Show | 10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1270+27T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780796 | ||||||
| chr8:28781060
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(61): Show | 65 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1099-66G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781060 | ||||||
| chr8:28781179
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-185G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781179 | ||||||
| chr8:28781223
|
G | A | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1099-229C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781223 | ||||||
| chr8:28781296
|
G | A | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-302C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781296 | ||||||
| chr8:28781396
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1099-402C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781396 | ||||||
| chr8:28781587
|
C | T | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1099-593G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781587 | ||||||
| chr8:28781627
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-633G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781627 | ||||||
| chr8:28781752
|
G | T | 9 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0111others(6): Show | 10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-758C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781752 | ||||||
| chr8:28781758
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1099-764G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781758 | ||||||
| chr8:28781851
|
G | A | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1099-857C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781851 | ||||||
| chr8:28781859
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1099-865C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781859 | ||||||
| chr8:28781884
|
T | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-890A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781884 | ||||||
| chr8:28781927
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1099-933G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781927 | ||||||
| chr8:28781943
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-949G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781943 | ||||||
| chr8:28781944
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1099-950C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781944 | ||||||
| chr8:28781952
|
G | A | 2 | a0001c0001t0001g0345a0001c0001t0001g0352 | 2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1099-958C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781952 | ||||||
| chr8:28781953
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1099-959A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781953 | ||||||
| chr8:28781967
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1099-973C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781967 | ||||||
| chr8:28782019
|
T | A | 3 | a0001c0001t0005g0162a0001c0001t0005g0177a0003c0008t0001g0006 | 3 | HG02965.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1099-1025A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782019 | ||||||
| chr8:28782042
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-1048C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782042 | ||||||
| chr8:28782288
|
T | A | 13 | a0001c0001t0001g0180a0001c0001t0001g0211a0001c0001t0001g0226others(10): Show | 13 | NA18612.hp2 NA18944.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-1294A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782288 | ||||||
| chr8:28782304
|
C | G | 15 | a0001c0001t0001g0287a0001c0001t0001g0345a0001c0001t0001g0352others(12): Show | 15 | HG01261.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-1310G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782304 | ||||||
| chr8:28782352
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1099-1358A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782352 | ||||||
| chr8:28782353
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1099-1359G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782353 | ||||||
| chr8:28782507
|
T | C | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1513A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782507 | ||||||
| chr8:28782539
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-1545C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782539 | ||||||
| chr8:28782770
|
C | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1099-1776G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782770 | ||||||
| chr8:28782833
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG01346.hp1 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-1839T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782833 | ||||||
| chr8:28782853
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(118): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1099-1859C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782853 | ||||||
| chr8:28782870
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-1876T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782870 | ||||||
| chr8:28783031
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1099-2037C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783031 | ||||||
| chr8:28783093
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1099-2099G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783093 | ||||||
| chr8:28783102
|
G | A | 11 | a0001c0001t0001g0287a0001c0001t0001g0343a0001c0001t0001g0345others(8): Show | 11 | HG01261.hp1 HG02451.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-2108C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783102 | ||||||
| chr8:28783109
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1099-2115G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783109 | ||||||
| chr8:28783142
|
C | CA | 17 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(14): Show | 17 | HG01261.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-2149dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
C | CAA | 11 | a0001c0001t0001g0050a0001c0001t0001g0109a0001c0001t0001g0345others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-2150_1099-214 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CA | C | 54 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(51): Show | 55 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1099-2149delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CAAA | C | 26 | a0001c0001t0001g0156a0001c0001t0001g0173a0001c0001t0001g0201others(23): Show | 27 | HG00597.hp2 HG00738.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1099-2151_1099-214 others(7): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CAAAA | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(95): Show | 100 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1099-2152_1099-214 others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CAAAAA | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0242a0001c0001t0001g0256others(3): Show | 6 | HG02258.hp1 HG02976.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-2153_1099-214 others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0185others(9): Show | 12 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1099-2159_1099-214 others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CAAAAAAA others(5): Show |
C | 82 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1099-2160_1099-214 others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783142
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0005g0162a0001c0001t0005g0177a0003c0008t0001g0006 | 3 | HG02965.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1099-2161_1099-214 others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | ||||||
| chr8:28783183
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-2189G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783183 | ||||||
| chr8:28783188
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-2194G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783188 | ||||||
| chr8:28783242
|
T | C | 352 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(349): Show | 357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1099-2248A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783242 | ||||||
| chr8:28783254
|
A | G | 24 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(21): Show | 24 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1099-2260T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783254 | ||||||
| chr8:28783568
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1099-2574C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783568 | ||||||
| chr8:28783658
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1099-2664C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783658 | ||||||
| chr8:28783670
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1099-2676C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783670 | ||||||
| chr8:28783693
|
T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-2699A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783693 | ||||||
| chr8:28783855
|
T | C | 9 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0111others(6): Show | 10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-2861A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783855 | ||||||
| chr8:28783885
|
A | C | 2 | a0001c0001t0001g0300a0001c0001t0001g0303 | 2 | NA18941.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1099-2891T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783885 | ||||||
| chr8:28783898
|
G | C | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-2904C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783898 | ||||||
| chr8:28784011
|
T | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-3017A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784011 | ||||||
| chr8:28784132
|
T | A | 24 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(21): Show | 24 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1099-3138A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784132 | ||||||
| chr8:28784162
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1099-3168T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784162 | ||||||
| chr8:28784205
|
C | T | 5 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-3211G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784205 | ||||||
| chr8:28784207
|
A | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-3213T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784207 | ||||||
| chr8:28784221
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | NA18947.hp1 NA19007.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-3227T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784221 | ||||||
| chr8:28784704
|
G | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0224 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1098+3125C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784704 | ||||||
| chr8:28784705
|
G | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(117): Show | 122 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1098+3124C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784705 | ||||||
| chr8:28784758
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1098+3071G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784758 | ||||||
| chr8:28784954
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1098+2875G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784954 | ||||||
| chr8:28785069
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0045 | 2 | HG01074.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1098+2760A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785069 | ||||||
| chr8:28785140
|
G | A | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0185others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+2689C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785140 | ||||||
| chr8:28785188
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1098+2641G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785188 | ||||||
| chr8:28785244
|
A | G | 19 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1098+2585T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785244 | ||||||
| chr8:28785411
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1098+2418G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785411 | ||||||
| chr8:28785502
|
T | C | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+2327A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785502 | ||||||
| chr8:28785543
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(186): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1098+2286G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785543 | ||||||
| chr8:28785579
|
C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1098+2250G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785579 | ||||||
| chr8:28785620
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1098+2209G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785620 | ||||||
| chr8:28785664
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1098+2165G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785664 | ||||||
| chr8:28785709
|
C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1098+2120G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785709 | ||||||
| chr8:28785792
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1098+2037A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785792 | ||||||
| chr8:28785904
|
G | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(183): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1098+1925C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785904 | ||||||
| chr8:28785940
|
G | A | 2 | a0001c0001t0001g0281a0001c0005t0001g0293 | 2 | HG02559.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1098+1889C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785940 | ||||||
| chr8:28786205
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1098+1624A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786205 | ||||||
| chr8:28786226
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+1603G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786226 | ||||||
| chr8:28786300
|
G | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(63): Show | 67 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1098+1529C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786300 | ||||||
| chr8:28786327
|
A | G | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+1502T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786327 | ||||||
| chr8:28786352
|
T | G | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1098+1477A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786352 | ||||||
| chr8:28786583
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1098+1246C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786583 | ||||||
| chr8:28786672
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1098+1157G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786672 | ||||||
| chr8:28786729
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+1100A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786729 | ||||||
| chr8:28786766
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1098+1063T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786766 | ||||||
| chr8:28786829
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1098+1000A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786829 | ||||||
| chr8:28786863
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+966T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786863 | ||||||
| chr8:28786908
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1098+921C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786908 | ||||||
| chr8:28786952
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1098+877A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786952 | ||||||
| chr8:28786960
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1098+869T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786960 | ||||||
| chr8:28787007
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(1): Show | 4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+822C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787007 | ||||||
| chr8:28787013
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1098+816T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787013 | ||||||
| chr8:28787117
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1098+712A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787117 | ||||||
| chr8:28787141
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+688G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787141 | ||||||
| chr8:28787154
|
TCATAATA others(4): Show |
T | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+664_1098+674d others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787154 | ||||||
| chr8:28787254
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1098+575T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787254 | ||||||
| chr8:28787301
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1098+528A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787301 | ||||||
| chr8:28787440
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0057others(118): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1098+389C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787440 | ||||||
| chr8:28787626
|
G | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0345others(6): Show | 9 | HG01261.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+203C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787626 | ||||||
| chr8:28787681
|
TA | T | 14 | a0001c0001t0001g0287a0001c0001t0001g0343a0001c0001t0002g0146others(11): Show | 14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+147delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787681 | ||||||
| chr8:28787754
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1098+75G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787754 | ||||||
| chr8:28787971
|
T | C | 7 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038-82A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28787971 | ||||||
| chr8:28788048
|
G | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1038-159C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788048 | ||||||
| chr8:28788153
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | NA18944.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1038-264T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788153 | ||||||
| chr8:28788156
|
G | C | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0072others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038-267C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788156 | ||||||
| chr8:28788171
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1038-282G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788171 | ||||||
| chr8:28788217
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1038-328G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788217 | ||||||
| chr8:28788306
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1038-417T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788306 | ||||||
| chr8:28788324
|
T | G | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038-435A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788324 | ||||||
| chr8:28788339
|
G | A | 2 | a0001c0001t0001g0317a0001c0001t0001g0337 | 2 | NA18963.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1038-450C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788339 | ||||||
| chr8:28788449
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1038-560G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788449 | ||||||
| chr8:28788562
|
G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1038-673C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788562 | ||||||
| chr8:28788691
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 80 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1038-802A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788691 | ||||||
| chr8:28788890
|
A | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1038-1001T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788890 | ||||||
| chr8:28788941
|
A | T | 3 | a0001c0003t0001g0136a0001c0003t0001g0316a0001c0003t0001g0351 | 3 | HG01261.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1038-1052T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788941 | ||||||
| chr8:28789092
|
A | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038-1203T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789092 | ||||||
| chr8:28789195
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1038-1306G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789195 | ||||||
| chr8:28789351
|
T | C | 22 | a0001c0001t0001g0050a0001c0001t0001g0104a0001c0001t0001g0105others(19): Show | 22 | HG00738.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1038-1462A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789351 | ||||||
| chr8:28789385
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1038-1496G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789385 | ||||||
| chr8:28789456
|
AGGAGATC others(49): Show |
A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG00140.hp1 HG00323.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-1623_1038-156 others(60): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789456 | ||||||
| chr8:28789514
|
T | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1038-1625A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789514 | ||||||
| chr8:28789767
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1038-1878T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789767 | ||||||
| chr8:28789880
|
AAACCAAC others(1): Show |
A | 97 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1038-1999_1038-199 others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789880 | ||||||
| chr8:28789909
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1038-2020T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789909 | ||||||
| chr8:28790315
|
A | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1038-2426T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790315 | ||||||
| chr8:28790475
|
G | A | 9 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0269others(6): Show | 9 | HG01358.hp1 HG01496.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038-2586C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790475 | ||||||
| chr8:28790513
|
A | C | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1038-2624T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790513 | ||||||
| chr8:28790579
|
T | C | 4 | a0001c0001t0001g0343a0001c0001t0002g0349a0001c0001t0003g0309others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-2690A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790579 | ||||||
| chr8:28790774
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1038-2885G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790774 | ||||||
| chr8:28790944
|
A | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+2863T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790944 | ||||||
| chr8:28790969
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+2838A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790969 | ||||||
| chr8:28790992
|
G | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(111): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1037+2815C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790992 | ||||||
| chr8:28791081
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+2726C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791081 | ||||||
| chr8:28791184
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1037+2623C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791184 | ||||||
| chr8:28791306
|
C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1037+2501G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791306 | ||||||
| chr8:28791437
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+2370A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791437 | ||||||
| chr8:28791466
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1037+2341G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791466 | ||||||
| chr8:28791617
|
G | A | 5 | a0001c0001t0001g0227a0001c0001t0001g0232a0001c0001t0001g0233others(2): Show | 5 | NA18747.hp1 NA18944.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037+2190C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791617 | ||||||
| chr8:28792048
|
G | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+1759C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792048 | ||||||
| chr8:28792062
|
G | A | 1 | a0001c0009t0001g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1037+1745C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792062 | ||||||
| chr8:28792148
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1037+1659G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792148 | ||||||
| chr8:28792269
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1037+1538T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792269 | ||||||
| chr8:28792336
|
A | C | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+1471T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792336 | ||||||
| chr8:28792552
|
C | CA | 128 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1037+1254dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792552 | ||||||
| chr8:28792769
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1037+1038G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792769 | ||||||
| chr8:28792782
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+1025C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792782 | ||||||
| chr8:28792907
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1037+900G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792907 | ||||||
| chr8:28792912
|
C | CA | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1037+894dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792912 | ||||||
| chr8:28792946
|
T | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+861A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792946 | ||||||
| chr8:28792984
|
A | AG | 9 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0089others(6): Show | 9 | HG00423.hp2 HG02071.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1037+822dupC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792984 | ||||||
| chr8:28792986
|
C | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1037+821G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792986 | ||||||
| chr8:28792991
|
A | G | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1037+816T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792991 | ||||||
| chr8:28793341
|
G | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0219others(6): Show | 10 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037+466C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793341 | ||||||
| chr8:28793412
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1037+395T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793412 | ||||||
| chr8:28793456
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1037+351T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793456 | ||||||
| chr8:28793776
|
T | TCA | 8 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0153others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1037+29_1037+30dup others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793776 | ||||||
| chr8:28793779
|
C | CA | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+27dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793779 | ||||||
| chr8:28793780
|
A | AC | 3 | a0001c0001t0001g0241a0001c0001t0001g0264a0001c0001t0001g0353 | 3 | HG00733.hp2 HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1037+26_1037+27ins others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793780 | ||||||
| chr8:28793781
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1037+26T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793781 | ||||||
| chr8:28793782
|
A | C | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1037+25T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793782 | ||||||
| chr8:28793783
|
A | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 76 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1037+24T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793783 | ||||||
| chr8:28793785
|
A | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0150 | 3 | HG01074.hp1 HG03041.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1037+22T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793785 | ||||||
| chr8:28793795
|
C | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0082a0001c0001t0001g0181 | 3 | HG02486.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1037+12G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793795 | ||||||
| chr8:28794040
|
TATAAAG | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.857-59_857-54delCT others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794040 | ||||||
| chr8:28794229
|
T | C | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.857-242A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794229 | ||||||
| chr8:28794284
|
G | A | 13 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0185others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.857-297C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794284 | ||||||
| chr8:28794523
|
G | A | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.857-536C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794523 | ||||||
| chr8:28794537
|
T | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.857-550A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794537 | ||||||
| chr8:28794730
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.857-743G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794730 | ||||||
| chr8:28794892
|
G | GT | 4 | a0001c0001t0001g0004a0001c0001t0001g0247a0001c0001t0001g0257others(1): Show | 5 | HG00597.hp2 HG00673.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-906dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794892 | ||||||
| chr8:28795092
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.857-1105G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795092 | ||||||
| chr8:28795093
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.857-1106C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795093 | ||||||
| chr8:28795210
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.857-1223C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795210 | ||||||
| chr8:28795247
|
C | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0188others(4): Show | 7 | HG02027.hp2 NA18941.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.857-1260G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795247 | ||||||
| chr8:28795338
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.856+1206G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795338 | ||||||
| chr8:28795407
|
C | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(113): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.856+1137G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795407 | ||||||
| chr8:28795512
|
C | A | 6 | a0001c0001t0002g0305a0001c0001t0003g0309a0001c0001t0003g0310others(3): Show | 6 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+1032G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795512 | ||||||
| chr8:28795554
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.856+990G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795554 | ||||||
| chr8:28795556
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856+988G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795556 | ||||||
| chr8:28795582
|
G | C | 7 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+962C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795582 | ||||||
| chr8:28795595
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.856+949C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795595 | ||||||
| chr8:28795614
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856+930A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795614 | ||||||
| chr8:28795639
|
C | CA | 13 | a0001c0001t0001g0017a0001c0001t0001g0071a0001c0001t0001g0100others(10): Show | 13 | HG00408.hp1 HG01928.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.856+904dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | ||||||
| chr8:28795639
|
CAAA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 77 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.856+902_856+904del others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | ||||||
| chr8:28795639
|
CAAAA | C | 24 | a0001c0001t0001g0056a0001c0001t0001g0101a0001c0001t0001g0147others(21): Show | 24 | HG00323.hp1 HG00738.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.856+901_856+904del others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | ||||||
| chr8:28795639
|
CAAAAA | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.856+900_856+904del others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | ||||||
| chr8:28795639
|
CAAAAAA | C | 7 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(4): Show | 7 | HG01261.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+899_856+904del others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | ||||||
| chr8:28795646
|
A | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.856+898T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795646 | ||||||
| chr8:28795742
|
GA | G | 3 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305 | 3 | HG02630.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.856+801delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795742 | ||||||
| chr8:28795824
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856+720C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795824 | ||||||
| chr8:28796051
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.856+493C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796051 | ||||||
| chr8:28796080
|
C | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0304a0001c0001t0001g0340 | 3 | HG00558.hp2 NA18993.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.856+464G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796080 | ||||||
| chr8:28796086
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0311 | 2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.856+458C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796086 | ||||||
| chr8:28796087
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.856+457T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796087 | ||||||
| chr8:28796112
|
C | T | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+432G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796112 | ||||||
| chr8:28796175
|
T | C | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856+369A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796175 | ||||||
| chr8:28796183
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.856+361C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796183 | ||||||
| chr8:28796237
|
C | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.856+307G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796237 | ||||||
| chr8:28796271
|
C | G | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.856+273G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796271 | ||||||
| chr8:28796317
|
C | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.856+227G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796317 | ||||||
| chr8:28796335
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+209T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796335 | ||||||
| chr8:28796411
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(120): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.856+133T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796411 | ||||||
| chr8:28796695
|
G | A | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-40C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796695 | ||||||
| chr8:28796791
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.745-136T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796791 | ||||||
| chr8:28796953
|
A | G | 7 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-298T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796953 | ||||||
| chr8:28796991
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.745-336A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796991 | ||||||
| chr8:28797088
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-433G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797088 | ||||||
| chr8:28797128
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.745-473C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797128 | ||||||
| chr8:28797188
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-533A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797188 | ||||||
| chr8:28797211
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.745-556T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797211 | ||||||
| chr8:28797289
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.745-634C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797289 | ||||||
| chr8:28797489
|
A | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.745-834T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797489 | ||||||
| chr8:28797563
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.745-908C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797563 | ||||||
| chr8:28797577
|
A | ACTCACCA others(119): Show |
1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.745-1048_745-923du others(127): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797577 | ||||||
| chr8:28797603
|
G | T | 4 | a0001c0001t0001g0343a0001c0003t0001g0136a0001c0003t0001g0316others(1): Show | 4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-948C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797603 | ||||||
| chr8:28797724
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.745-1069C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797724 | ||||||
| chr8:28797898
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.745-1243A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797898 | ||||||
| chr8:28797915
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.745-1260G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797915 | ||||||
| chr8:28797924
|
C | G | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-1269G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797924 | ||||||
| chr8:28798009
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.745-1354C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798009 | ||||||
| chr8:28798267
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-1612C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798267 | ||||||
| chr8:28798414
|
C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.745-1759G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798414 | ||||||
| chr8:28798519
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.745-1864A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798519 | ||||||
| chr8:28798615
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1960G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798615 | ||||||
| chr8:28798784
|
C | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.745-2129G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798784 | ||||||
| chr8:28798825
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.745-2170T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798825 | ||||||
| chr8:28798849
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.745-2194T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798849 | ||||||
| chr8:28798982
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(1): Show | 4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-2327C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798982 | ||||||
| chr8:28798986
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0328a0002c0006t0001g0325 | 3 | NA18962.hp1 NA19067.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.745-2331A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798986 | ||||||
| chr8:28799007
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745-2352T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799007 | ||||||
| chr8:28799021
|
G | C | 4 | a0001c0001t0001g0343a0001c0003t0001g0136a0001c0003t0001g0316others(1): Show | 4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-2366C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799021 | ||||||
| chr8:28799160
|
C | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.745-2505G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799160 | ||||||
| chr8:28799189
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.745-2534C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799189 | ||||||
| chr8:28799193
|
G | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-2538C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799193 | ||||||
| chr8:28799283
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.745-2628G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799283 | ||||||
| chr8:28799296
|
C | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(113): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.745-2641G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799296 | ||||||
| chr8:28799323
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.745-2668C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799323 | ||||||
| chr8:28799342
|
T | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.745-2687A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799342 | ||||||
| chr8:28799594
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-2939G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799594 | ||||||
| chr8:28799662
|
A | C | 4 | a0001c0001t0001g0343a0001c0003t0001g0136a0001c0003t0001g0316others(1): Show | 4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3007T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799662 | ||||||
| chr8:28799676
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-3021G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799676 | ||||||
| chr8:28799677
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG00642.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.745-3022C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799677 | ||||||
| chr8:28799984
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-3329C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799984 | ||||||
| chr8:28800064
|
G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-3409C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800064 | ||||||
| chr8:28800093
|
T | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.745-3438A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800093 | ||||||
| chr8:28800244
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.745-3589C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800244 | ||||||
| chr8:28800481
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.745-3826T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800481 | ||||||
| chr8:28800559
|
T | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.745-3904A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800559 | ||||||
| chr8:28800559
|
T | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.745-3904A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800559 | ||||||
| chr8:28800704
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.745-4049G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800704 | ||||||
| chr8:28800860
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-4205G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800860 | ||||||
| chr8:28800998
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0190 | 2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.745-4343T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800998 | ||||||
| chr8:28801047
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.745-4392G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801047 | ||||||
| chr8:28801134
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-4479C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801134 | ||||||
| chr8:28801173
|
T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745-4518A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801173 | ||||||
| chr8:28801315
|
C | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-4660G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801315 | ||||||
| chr8:28801339
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.745-4684T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801339 | ||||||
| chr8:28801340
|
A | G | 4 | a0001c0001t0001g0343a0001c0003t0001g0136a0001c0003t0001g0316others(1): Show | 4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-4685T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801340 | ||||||
| chr8:28801348
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.745-4693C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801348 | ||||||
| chr8:28801505
|
AC | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.745-4851delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801505 | ||||||
| chr8:28801506
|
C | A | 20 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0065others(17): Show | 20 | HG01070.hp2 HG01261.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.745-4851G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801506 | ||||||
| chr8:28801506
|
CA | C | 7 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-4852delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801506 | ||||||
| chr8:28801513
|
A | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0263a0001c0001t0005g0162others(1): Show | 4 | HG02055.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-4858T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801513 | ||||||
| chr8:28801514
|
C | A | 3 | a0001c0001t0001g0263a0001c0001t0005g0162a0001c0001t0005g0177 | 3 | HG03516.hp2 NA18522.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.745-4859G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801514 | ||||||
| chr8:28801531
|
A | C | 7 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-4876T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801531 | ||||||
| chr8:28801540
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.745-4885A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801540 | ||||||
| chr8:28801983
|
G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.745-5328C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801983 | ||||||
| chr8:28802002
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.745-5347A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802002 | ||||||
| chr8:28802047
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745-5392G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802047 | ||||||
| chr8:28802217
|
G | C | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-5562C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802217 | ||||||
| chr8:28802238
|
A | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(113): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.745-5583T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802238 | ||||||
| chr8:28802370
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.745-5715G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802370 | ||||||
| chr8:28802385
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.745-5730C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802385 | ||||||
| chr8:28802446
|
C | G | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.745-5791G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802446 | ||||||
| chr8:28802693
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(119): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.745-6038T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802693 | ||||||
| chr8:28802946
|
C | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.745-6291G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802946 | ||||||
| chr8:28802946
|
C | CA | 24 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0032others(21): Show | 25 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.745-6292dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802946 | ||||||
| chr8:28802946
|
C | CAA | 7 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-6293_745-6292d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802946 | ||||||
| chr8:28802975
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.745-6320A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802975 | ||||||
| chr8:28803378
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745-6723G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803378 | ||||||
| chr8:28803379
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.745-6724T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803379 | ||||||
| chr8:28803491
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00621.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.745-6836C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803491 | ||||||
| chr8:28803679
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.745-7024A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803679 | ||||||
| chr8:28803769
|
G | C | 3 | a0001c0003t0001g0136a0001c0003t0001g0316a0001c0003t0001g0351 | 3 | HG01261.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.745-7114C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803769 | ||||||
| chr8:28803855
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-7200A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803855 | ||||||
| chr8:28803986
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-7331G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803986 | ||||||
| chr8:28804011
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-7356G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804011 | ||||||
| chr8:28804026
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.745-7371G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804026 | ||||||
| chr8:28804246
|
G | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.745-7591C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804246 | ||||||
| chr8:28804260
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.745-7605C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804260 | ||||||
| chr8:28804273
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.745-7618C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804273 | ||||||
| chr8:28804294
|
A | T | 2 | a0001c0001t0002g0350a0001c0005t0001g0293 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.745-7639T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804294 | ||||||
| chr8:28804467
|
G | A | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-7812C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804467 | ||||||
| chr8:28804530
|
A | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.744+7797T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804530 | ||||||
| chr8:28804559
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.744+7768C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804559 | ||||||
| chr8:28804583
|
G | A | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.744+7744C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804583 | ||||||
| chr8:28804650
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0212 | 3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.744+7677C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804650 | ||||||
| chr8:28804682
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.744+7645C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804682 | ||||||
| chr8:28804901
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.744+7426T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804901 | ||||||
| chr8:28805016
|
T | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+7311A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805016 | ||||||
| chr8:28805121
|
A | G | 8 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0153others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+7206T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805121 | ||||||
| chr8:28805161
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.744+7166T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805161 | ||||||
| chr8:28805229
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.744+7098C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805229 | ||||||
| chr8:28805373
|
C | CT | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+6953dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805373 | ||||||
| chr8:28805497
|
A | G | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.744+6830T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805497 | ||||||
| chr8:28805575
|
T | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(111): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.744+6752A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805575 | ||||||
| chr8:28805807
|
C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.744+6520G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805807 | ||||||
| chr8:28805838
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.744+6489T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805838 | ||||||
| chr8:28805906
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.744+6421C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805906 | ||||||
| chr8:28806026
|
T | G | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+6301A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806026 | ||||||
| chr8:28806086
|
C | CA | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 118 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.744+6240dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806086 | ||||||
| chr8:28806222
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.744+6105G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806222 | ||||||
| chr8:28806437
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.744+5890G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806437 | ||||||
| chr8:28806480
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.744+5847G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806480 | ||||||
| chr8:28806506
|
TAA | T | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+5819_744+5820d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806506 | ||||||
| chr8:28806538
|
A | G | 1 | a0002c0006t0001g0325 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.744+5789T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806538 | ||||||
| chr8:28806587
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.744+5740G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806587 | ||||||
| chr8:28806721
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.744+5606A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806721 | ||||||
| chr8:28806789
|
C | T | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0072others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.744+5538G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806789 | ||||||
| chr8:28806843
|
G | A | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+5484C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806843 | ||||||
| chr8:28806960
|
G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+5367C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806960 | ||||||
| chr8:28807072
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.744+5255A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807072 | ||||||
| chr8:28807073
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.744+5254C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807073 | ||||||
| chr8:28807102
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.744+5225A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807102 | ||||||
| chr8:28807602
|
T | G | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+4725A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807602 | ||||||
| chr8:28807706
|
T | C | 8 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0153others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+4621A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807706 | ||||||
| chr8:28807744
|
C | A | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+4583G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807744 | ||||||
| chr8:28807958
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.744+4369A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807958 | ||||||
| chr8:28807991
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.744+4336T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807991 | ||||||
| chr8:28808193
|
AT | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0001g0266others(4): Show | 7 | HG02572.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+4133delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808193 | ||||||
| chr8:28808193
|
ATT | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.744+4132_744+4133d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808193 | ||||||
| chr8:28808251
|
T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.744+4076A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808251 | ||||||
| chr8:28808378
|
A | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+3949T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808378 | ||||||
| chr8:28808420
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.744+3907C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808420 | ||||||
| chr8:28808480
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00621.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.744+3847C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808480 | ||||||
| chr8:28808496
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.744+3831G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808496 | ||||||
| chr8:28808528
|
C | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.744+3799G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808528 | ||||||
| chr8:28808752
|
G | A | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+3575C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808752 | ||||||
| chr8:28808765
|
G | A | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3562C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808765 | ||||||
| chr8:28808812
|
C | G | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3515G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808812 | ||||||
| chr8:28808929
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.744+3398T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808929 | ||||||
| chr8:28808952
|
C | CT | 9 | a0001c0001t0001g0078a0001c0001t0001g0125a0001c0001t0001g0127others(6): Show | 9 | HG01069.hp1 HG01346.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+3374dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808952 | ||||||
| chr8:28808952
|
CT | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.744+3374delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808952 | ||||||
| chr8:28809023
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.744+3304G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809023 | ||||||
| chr8:28809024
|
AC | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.744+3302delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809024 | ||||||
| chr8:28809026
|
T | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.744+3301A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809026 | ||||||
| chr8:28809118
|
T | C | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.744+3209A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809118 | ||||||
| chr8:28809121
|
T | A | 17 | a0001c0001t0001g0156a0001c0001t0002g0164a0001c0001t0002g0165others(14): Show | 18 | HG00738.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.744+3206A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809121 | ||||||
| chr8:28809143
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(109): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.744+3184C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809143 | ||||||
| chr8:28809198
|
A | G | 1 | a0001c0001t0001g0323 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.744+3129T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809198 | ||||||
| chr8:28809265
|
G | A | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3062C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809265 | ||||||
| chr8:28809312
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.744+3015A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809312 | ||||||
| chr8:28809455
|
C | G | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+2872G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809455 | ||||||
| chr8:28809658
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.744+2669G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809658 | ||||||
| chr8:28809820
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.744+2507G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809820 | ||||||
| chr8:28809849
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.744+2478G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809849 | ||||||
| chr8:28809978
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.744+2349A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809978 | ||||||
| chr8:28810104
|
T | C | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+2223A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810104 | ||||||
| chr8:28810331
|
A | T | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.744+1996T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810331 | ||||||
| chr8:28810352
|
T | TA | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.744+1974dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810352 | ||||||
| chr8:28810422
|
C | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG00733.hp2 HG01074.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+1905G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810422 | ||||||
| chr8:28810429
|
G | C | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.744+1898C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810429 | ||||||
| chr8:28810520
|
C | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.744+1807G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810520 | ||||||
| chr8:28810600
|
TTCTCTC | T | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1721_744+1726d others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810600 | ||||||
| chr8:28810604
|
C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+1723G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810604 | ||||||
| chr8:28810781
|
C | CT | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(119): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.744+1545_744+1546i others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810781 | ||||||
| chr8:28810866
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+1461G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810866 | ||||||
| chr8:28811099
|
TTC | T | 21 | a0001c0001t0001g0156a0001c0001t0002g0164a0001c0001t0002g0165others(18): Show | 22 | HG00738.hp2 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.744+1226_744+1227d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811099 | ||||||
| chr8:28811128
|
CT | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0039others(22): Show | 26 | HG00738.hp2 HG01243.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.744+1198delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811128 | ||||||
| chr8:28811128
|
CTT | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(113): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.744+1197_744+1198d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811128 | ||||||
| chr8:28811221
|
G | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0070a0001c0001t0001g0071others(6): Show | 9 | HG01346.hp1 HG01928.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+1106C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811221 | ||||||
| chr8:28811251
|
C | T | 1 | a0001c0001t0007g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.744+1076G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811251 | ||||||
| chr8:28811308
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.744+1019C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811308 | ||||||
| chr8:28811406
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.744+921C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811406 | ||||||
| chr8:28811423
|
CT | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.744+903delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811423 | ||||||
| chr8:28811465
|
G | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.744+862C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811465 | ||||||
| chr8:28811475
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.744+852T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811475 | ||||||
| chr8:28811940
|
C | T | 1 | a0001c0002t0003g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.744+387G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811940 | ||||||
| chr8:28811941
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0263 | 2 | NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.744+386C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811941 | ||||||
| chr8:28812219
|
A | G | 10 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.744+108T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28812219 | ||||||
| chr8:28812223
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+104G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28812223 | ||||||
| chr8:28812493
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0259 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.610-32C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812493 | ||||||
| chr8:28812779
|
A | C | 1 | a0001c0001t0001g0290 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.610-318T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812779 | ||||||
| chr8:28812804
|
T | G | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.610-343A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812804 | ||||||
| chr8:28812827
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.610-366T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812827 | ||||||
| chr8:28812907
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.610-446C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812907 | ||||||
| chr8:28813022
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.609+470C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813022 | ||||||
| chr8:28813229
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.609+263A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813229 | ||||||
| chr8:28813245
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.609+247G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813245 | ||||||
| chr8:28813266
|
G | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.609+226C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813266 | ||||||
| chr8:28813278
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.609+214G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813278 | ||||||
| chr8:28813321
|
G | A | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.609+171C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813321 | ||||||
| chr8:28813679
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489-67T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813679 | ||||||
| chr8:28813705
|
G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-93C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813705 | ||||||
| chr8:28813730
|
T | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-118A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813730 | ||||||
| chr8:28813785
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-173T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813785 | ||||||
| chr8:28813813
|
T | C | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-201A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813813 | ||||||
| chr8:28813821
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(1): Show | 4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-209G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813821 | ||||||
| chr8:28813830
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489-218C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813830 | ||||||
| chr8:28813868
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.489-256G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813868 | ||||||
| chr8:28814060
|
T | A | 2 | a0001c0003t0001g0136a0001c0003t0001g0351 | 2 | HG01261.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.489-448A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814060 | ||||||
| chr8:28814070
|
T | A | 17 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0069others(14): Show | 17 | HG01261.hp1 HG02109.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.489-458A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814070 | ||||||
| chr8:28814070
|
T | TA | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0219others(6): Show | 10 | HG02165.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-459dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814070 | ||||||
| chr8:28814070
|
TA | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0123others(20): Show | 24 | HG01069.hp1 HG01081.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.489-459delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814070 | ||||||
| chr8:28814238
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.489-626G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814238 | ||||||
| chr8:28814282
|
TCTCACAC others(5): Show |
T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489-682_489-671del others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814282 | ||||||
| chr8:28814284
|
T | A | 3 | a0001c0001t0002g0146a0001c0001t0002g0274a0004c0004t0002g0315 | 3 | HG02809.hp2 HG02965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.489-672A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
T | TCA | 29 | a0001c0001t0001g0004a0001c0001t0001g0067a0001c0001t0001g0112others(26): Show | 30 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.489-674_489-673dup others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
T | TCACA | 18 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0104others(15): Show | 18 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.489-676_489-673dup others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
T | TCACACA | 6 | a0001c0001t0001g0068a0001c0001t0001g0110a0001c0001t0001g0117others(3): Show | 6 | HG00738.hp1 HG01255.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-678_489-673dup others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0174 | 3 | HG01070.hp1 HG02258.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.489-682_489-673dup others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCA | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0015others(46): Show | 52 | HG01168.hp1 HG01256.hp1 HG01358.hp1 others(49): Show |
intron_variant | MODIFIER | c.489-674_489-673del others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACA | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0070others(34): Show | 37 | HG00280.hp2 HG00733.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.489-676_489-673del others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACA | T | 88 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.489-678_489-673del others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(1): Show |
T | 39 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 40 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.489-680_489-673del others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(3): Show |
T | 6 | a0001c0001t0001g0059a0001c0001t0001g0097a0001c0001t0001g0199others(3): Show | 6 | HG00738.hp2 HG01070.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-682_489-673del others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(5): Show |
T | 5 | a0001c0001t0001g0047a0001c0001t0001g0187a0001c0001t0002g0164others(2): Show | 5 | HG01243.hp2 HG01358.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-684_489-673del others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(9): Show |
T | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489-688_489-673del others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(11): Show |
T | 3 | a0001c0001t0001g0185a0001c0001t0001g0203a0001c0001t0001g0347 | 3 | HG01069.hp1 HG01167.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.489-690_489-673del others(18): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(13): Show |
T | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0186others(7): Show | 10 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-692_489-673del others(20): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814284
|
TCACACAC others(15): Show |
T | 2 | a0001c0001t0001g0007a0001c0001t0008g0194 | 2 | HG02451.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.489-694_489-673del others(22): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | ||||||
| chr8:28814288
|
A | T | 6 | a0001c0001t0004g0002a0001c0001t0004g0153a0001c0001t0004g0154others(3): Show | 7 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-676T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814288 | ||||||
| chr8:28814290
|
A | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489-678T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814290 | ||||||
| chr8:28814296
|
A | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.489-684T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814296 | ||||||
| chr8:28814334
|
A | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489-722T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814334 | ||||||
| chr8:28814341
|
C | T | 24 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 24 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.489-729G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814341 | ||||||
| chr8:28814547
|
T | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-935A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814547 | ||||||
| chr8:28814591
|
C | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489-979G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814591 | ||||||
| chr8:28814703
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.489-1091C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814703 | ||||||
| chr8:28814756
|
T | C | 1 | a0001c0001t0001g0327 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.489-1144A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814756 | ||||||
| chr8:28814844
|
G | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(109): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-1232C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814844 | ||||||
| chr8:28814938
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.489-1326A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814938 | ||||||
| chr8:28815019
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489-1407G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815019 | ||||||
| chr8:28815071
|
G | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-1459C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815071 | ||||||
| chr8:28815146
|
C | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-1534G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815146 | ||||||
| chr8:28815162
|
T | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-1550A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815162 | ||||||
| chr8:28815325
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.489-1713C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815325 | ||||||
| chr8:28815325
|
G | T | 11 | a0001c0001t0001g0156a0001c0001t0002g0349a0001c0001t0003g0309others(8): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.489-1713C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815325 | ||||||
| chr8:28815380
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489-1768G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815380 | ||||||
| chr8:28815594
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-1982C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815594 | ||||||
| chr8:28815723
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-2111G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815723 | ||||||
| chr8:28815863
|
C | T | 8 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-2251G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815863 | ||||||
| chr8:28815872
|
A | C | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-2260T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815872 | ||||||
| chr8:28815929
|
A | T | 1 | a0001c0009t0001g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.489-2317T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815929 | ||||||
| chr8:28816155
|
A | C | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-2543T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816155 | ||||||
| chr8:28816230
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.489-2618C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816230 | ||||||
| chr8:28816260
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489-2648C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816260 | ||||||
| chr8:28816449
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.489-2837G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816449 | ||||||
| chr8:28816456
|
G | A | 10 | a0001c0001t0001g0156a0001c0001t0003g0309a0001c0001t0003g0310others(7): Show | 11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-2844C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816456 | ||||||
| chr8:28816458
|
C | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0073 | 3 | HG00639.hp1 HG01069.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.489-2846G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816458 | ||||||
| chr8:28816462
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(109): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-2850C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816462 | ||||||
| chr8:28816527
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.489-2915G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816527 | ||||||
| chr8:28816602
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489-2990G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816602 | ||||||
| chr8:28816604
|
C | G | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489-2992G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816604 | ||||||
| chr8:28816633
|
T | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-3021A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816633 | ||||||
| chr8:28816640
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-3028T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816640 | ||||||
| chr8:28816644
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-3032G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816644 | ||||||
| chr8:28816723
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489-3111G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816723 | ||||||
| chr8:28816724
|
G | A | 10 | a0001c0001t0001g0156a0001c0001t0003g0309a0001c0001t0003g0310others(7): Show | 11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-3112C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816724 | ||||||
| chr8:28816814
|
T | C | 2 | a0001c0001t0002g0274a0004c0004t0002g0315 | 2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.489-3202A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816814 | ||||||
| chr8:28816921
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(109): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-3309A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816921 | ||||||
| chr8:28817052
|
T | C | 8 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0153others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.489-3440A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817052 | ||||||
| chr8:28817078
|
C | T | 3 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305 | 3 | HG02630.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.489-3466G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817078 | ||||||
| chr8:28817419
|
C | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-3807G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817419 | ||||||
| chr8:28817476
|
G | A | 2 | a0001c0001t0002g0349a0001c0001t0004g0111 | 2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489-3864C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817476 | ||||||
| chr8:28817563
|
C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489-3951G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817563 | ||||||
| chr8:28817586
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-3974G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817586 | ||||||
| chr8:28817629
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.489-4017C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817629 | ||||||
| chr8:28817723
|
TGAATCTA others(61): Show |
T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(109): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-4179_489-4112d others(70): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817723 | ||||||
| chr8:28817805
|
T | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-4193A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817805 | ||||||
| chr8:28817838
|
T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-4226A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817838 | ||||||
| chr8:28817882
|
G | A | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.489-4270C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817882 | ||||||
| chr8:28818222
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.489-4610G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818222 | ||||||
| chr8:28818253
|
G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-4641C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818253 | ||||||
| chr8:28818275
|
A | G | 5 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-4663T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818275 | ||||||
| chr8:28818434
|
G | A | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-4822C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818434 | ||||||
| chr8:28818483
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.489-4871A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818483 | ||||||
| chr8:28818564
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489-4952A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818564 | ||||||
| chr8:28818581
|
A | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-4969T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818581 | ||||||
| chr8:28818613
|
C | G | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-5001G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818613 | ||||||
| chr8:28818635
|
C | A | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489-5023G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818635 | ||||||
| chr8:28818694
|
T | C | 11 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0203others(8): Show | 11 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-5082A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818694 | ||||||
| chr8:28818737
|
C | T | 1 | a0001c0009t0001g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.489-5125G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818737 | ||||||
| chr8:28818791
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.489-5179A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818791 | ||||||
| chr8:28819159
|
C | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-5547G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819159 | ||||||
| chr8:28819172
|
A | T | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-5560T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819172 | ||||||
| chr8:28819247
|
G | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.489-5635C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819247 | ||||||
| chr8:28819485
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.489-5873T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819485 | ||||||
| chr8:28819503
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0248a0001c0001t0001g0301 | 3 | NA18949.hp2 NA18960.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.489-5891G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819503 | ||||||
| chr8:28819628
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.489-6016A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819628 | ||||||
| chr8:28819670
|
T | C | 2 | a0001c0001t0001g0352a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.489-6058A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819670 | ||||||
| chr8:28819688
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.489-6076C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819688 | ||||||
| chr8:28819867
|
T | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-6255A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819867 | ||||||
| chr8:28819966
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0265 | 2 | HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.489-6354C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819966 | ||||||
| chr8:28819996
|
A | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-6384T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819996 | ||||||
| chr8:28820251
|
T | C | 2 | a0001c0003t0001g0136a0001c0003t0001g0351 | 2 | HG01261.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.489-6639A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820251 | ||||||
| chr8:28820410
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.489-6798A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820410 | ||||||
| chr8:28820430
|
A | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.489-6818T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820430 | ||||||
| chr8:28820582
|
G | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-6970C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820582 | ||||||
| chr8:28820607
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.489-6995C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820607 | ||||||
| chr8:28820657
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.489-7045T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820657 | ||||||
| chr8:28820815
|
T | C | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-7203A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820815 | ||||||
| chr8:28820849
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-7237C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820849 | ||||||
| chr8:28820850
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-7238C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820850 | ||||||
| chr8:28820916
|
TA | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-7305delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820916 | ||||||
| chr8:28821094
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-7482A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821094 | ||||||
| chr8:28821217
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-7605C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821217 | ||||||
| chr8:28821246
|
C | T | 67 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(64): Show | 68 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.489-7634G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821246 | ||||||
| chr8:28821255
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(88): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.489-7643G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821255 | ||||||
| chr8:28821303
|
T | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-7691A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821303 | ||||||
| chr8:28821348
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.489-7736C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821348 | ||||||
| chr8:28821456
|
C | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(110): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.489-7844G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821456 | ||||||
| chr8:28821575
|
A | AAAC | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-7966_489-7964d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821575 | ||||||
| chr8:28821591
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0303 | 2 | NA18941.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.489-7979G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821591 | ||||||
| chr8:28821759
|
G | GT | 8 | a0001c0001t0001g0035a0001c0001t0001g0215a0001c0001t0001g0216others(5): Show | 8 | HG01981.hp1 HG03471.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.489-8148dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821759 | ||||||
| chr8:28821794
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489-8182T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821794 | ||||||
| chr8:28822016
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.489-8404G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822016 | ||||||
| chr8:28822292
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.489-8680C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822292 | ||||||
| chr8:28822303
|
CT | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(111): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.489-8692delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822303 | ||||||
| chr8:28822348
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.489-8736C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822348 | ||||||
| chr8:28822437
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-8825G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822437 | ||||||
| chr8:28822574
|
A | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-8962T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822574 | ||||||
| chr8:28822600
|
C | T | 10 | a0001c0001t0001g0156a0001c0001t0003g0309a0001c0001t0003g0310others(7): Show | 11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-8988G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822600 | ||||||
| chr8:28822815
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.489-9203C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822815 | ||||||
| chr8:28823012
|
C | T | 1 | a0001c0001t0006g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.489-9400G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823012 | ||||||
| chr8:28823049
|
T | C | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-9437A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823049 | ||||||
| chr8:28823252
|
C | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.489-9640G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823252 | ||||||
| chr8:28823349
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.489-9737C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823349 | ||||||
| chr8:28823482
|
T | A | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-9870A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823482 | ||||||
| chr8:28823499
|
G | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(62): Show | 66 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.489-9887C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823499 | ||||||
| chr8:28823500
|
T | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.489-9888A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823500 | ||||||
| chr8:28823540
|
T | A | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-9928A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823540 | ||||||
| chr8:28823595
|
AC | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(112): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.489-9984delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823595 | ||||||
| chr8:28823727
|
A | G | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-10115T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823727 | ||||||
| chr8:28823757
|
TAACTC | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(63): Show | 67 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.489-10150_489-1014 others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823757 | ||||||
| chr8:28823789
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.489-10177A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823789 | ||||||
| chr8:28823811
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-10199G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823811 | ||||||
| chr8:28823860
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.489-10248A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823860 | ||||||
| chr8:28824072
|
C | G | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-10460G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824072 | ||||||
| chr8:28824164
|
T | C | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489-10552A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824164 | ||||||
| chr8:28824195
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.489-10583C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824195 | ||||||
| chr8:28824247
|
A | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(65): Show | 69 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.489-10635T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824247 | ||||||
| chr8:28824447
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.489-10835G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824447 | ||||||
| chr8:28824705
|
T | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488+10587A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824705 | ||||||
| chr8:28824712
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.488+10580G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824712 | ||||||
| chr8:28824791
|
G | C | 1 | a0001c0001t0001g0313 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.488+10501C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824791 | ||||||
| chr8:28824919
|
T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+10373A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824919 | ||||||
| chr8:28825033
|
C | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.488+10259G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825033 | ||||||
| chr8:28825077
|
G | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.488+10215C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825077 | ||||||
| chr8:28825190
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.488+10102A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825190 | ||||||
| chr8:28825204
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.488+10088A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825204 | ||||||
| chr8:28825304
|
G | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.488+9988C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825304 | ||||||
| chr8:28825511
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0002g0349a0001c0001t0003g0309others(8): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.488+9781G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825511 | ||||||
| chr8:28825734
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.488+9558A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825734 | ||||||
| chr8:28825783
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(111): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.488+9509G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825783 | ||||||
| chr8:28825846
|
G | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.488+9446C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825846 | ||||||
| chr8:28825852
|
C | A | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.488+9440G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825852 | ||||||
| chr8:28825963
|
C | G | 11 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0072others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.488+9329G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825963 | ||||||
| chr8:28826045
|
A | G | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(112): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.488+9247T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826045 | ||||||
| chr8:28826079
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | NA18973.hp1 NA18999.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.488+9213G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826079 | ||||||
| chr8:28826111
|
A | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+9181T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826111 | ||||||
| chr8:28826114
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.488+9178C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826114 | ||||||
| chr8:28826311
|
A | G | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.488+8981T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826311 | ||||||
| chr8:28826312
|
T | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(62): Show | 66 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.488+8980A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826312 | ||||||
| chr8:28826356
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488+8936G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826356 | ||||||
| chr8:28826445
|
G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.488+8847C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826445 | ||||||
| chr8:28826451
|
G | C | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.488+8841C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826451 | ||||||
| chr8:28826463
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0352 | 3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.488+8829G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826463 | ||||||
| chr8:28826497
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+8795C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826497 | ||||||
| chr8:28826689
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0352 | 3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.488+8603G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826689 | ||||||
| chr8:28827090
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.488+8202C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827090 | ||||||
| chr8:28827354
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.488+7938C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827354 | ||||||
| chr8:28827356
|
G | GT | 8 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+7935dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827356 | ||||||
| chr8:28827466
|
G | A | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(121): Show | 127 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.488+7826C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827466 | ||||||
| chr8:28827511
|
G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.488+7781C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827511 | ||||||
| chr8:28827643
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.488+7649C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827643 | ||||||
| chr8:28827656
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488+7636G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827656 | ||||||
| chr8:28827675
|
C | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(120): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.488+7617G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827675 | ||||||
| chr8:28827704
|
G | T | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.488+7588C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827704 | ||||||
| chr8:28827812
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.488+7480A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827812 | ||||||
| chr8:28827865
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.488+7427A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827865 | ||||||
| chr8:28827962
|
G | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.488+7330C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827962 | ||||||
| chr8:28827968
|
G | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488+7324C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827968 | ||||||
| chr8:28827970
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.488+7322T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827970 | ||||||
| chr8:28828058
|
G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.488+7234C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828058 | ||||||
| chr8:28828099
|
C | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7193G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828099 | ||||||
| chr8:28828100
|
T | G | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7192A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828100 | ||||||
| chr8:28828101
|
C | G | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7191G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828101 | ||||||
| chr8:28828102
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7190A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828102 | ||||||
| chr8:28828123
|
T | G | 8 | a0001c0001t0001g0156a0001c0001t0004g0002a0001c0001t0004g0153others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.488+7169A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828123 | ||||||
| chr8:28828541
|
C | A | 5 | a0001c0001t0001g0287a0001c0001t0002g0146a0001c0001t0002g0274others(2): Show | 5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+6751G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828541 | ||||||
| chr8:28828571
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(3): Show | 6 | HG00621.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.488+6721C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828571 | ||||||
| chr8:28828706
|
T | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+6586A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828706 | ||||||
| chr8:28829084
|
T | G | 5 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+6208A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829084 | ||||||
| chr8:28829154
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.488+6138G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829154 | ||||||
| chr8:28829379
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0085 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.488+5913C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829379 | ||||||
| chr8:28829450
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.488+5842T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829450 | ||||||
| chr8:28829667
|
A | G | 4 | a0001c0001t0001g0345a0001c0001t0002g0262a0001c0001t0002g0305others(1): Show | 4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+5625T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829667 | ||||||
| chr8:28829757
|
G | A | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0189others(2): Show | 5 | HG03041.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+5535C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829757 | ||||||
| chr8:28829780
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(98): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.488+5512G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829780 | ||||||
| chr8:28829838
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.488+5454A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829838 | ||||||
| chr8:28829919
|
A | G | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+5373T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829919 | ||||||
| chr8:28829954
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.488+5338G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829954 | ||||||
| chr8:28830052
|
G | GA | 86 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 87 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.488+5239dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830052 | ||||||
| chr8:28830096
|
G | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(296): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.488+5196C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830096 | ||||||
| chr8:28830208
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0088a0001c0001t0002g0028 | 3 | HG02717.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.488+5084T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830208 | ||||||
| chr8:28830525
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(112): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.488+4767C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830525 | ||||||
| chr8:28830632
|
T | TA | 9 | a0001c0001t0001g0188a0001c0001t0001g0287a0001c0001t0001g0290others(6): Show | 9 | HG00621.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.488+4659dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830632 | ||||||
| chr8:28830632
|
TA | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0025others(4): Show | 7 | HG00639.hp1 HG02615.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+4659delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830632 | ||||||
| chr8:28830655
|
T | C | 1 | a0001c0001t0001g0331 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.488+4637A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830655 | ||||||
| chr8:28830870
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.488+4422T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830870 | ||||||
| chr8:28830896
|
C | A | 5 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(2): Show | 5 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+4396G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830896 | ||||||
| chr8:28830897
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.488+4395G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830897 | ||||||
| chr8:28831050
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.488+4242C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831050 | ||||||
| chr8:28831184
|
T | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+4108A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831184 | ||||||
| chr8:28831314
|
C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.488+3978G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831314 | ||||||
| chr8:28831371
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+3921C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831371 | ||||||
| chr8:28831462
|
A | T | 10 | a0001c0001t0001g0343a0001c0001t0002g0164a0001c0001t0002g0165others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+3830T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831462 | ||||||
| chr8:28831499
|
G | A | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.488+3793C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831499 | ||||||
| chr8:28831589
|
A | T | 1 | a0001c0001t0001g0324 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.488+3703T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831589 | ||||||
| chr8:28831637
|
G | A | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0345others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+3655C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831637 | ||||||
| chr8:28831687
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.488+3605A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831687 | ||||||
| chr8:28831704
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.488+3588A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831704 | ||||||
| chr8:28831729
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0010t0003g0348 | 3 | HG02055.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.488+3563G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831729 | ||||||
| chr8:28831746
|
T | G | 1 | a0001c0001t0007g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.488+3546A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831746 | ||||||
| chr8:28831759
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+3533G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831759 | ||||||
| chr8:28831848
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.488+3444T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831848 | ||||||
| chr8:28831855
|
C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.488+3437G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831855 | ||||||
| chr8:28832232
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.488+3060G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832232 | ||||||
| chr8:28832460
|
G | A | 1 | a0001c0001t0004g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.488+2832C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832460 | ||||||
| chr8:28832617
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.488+2675C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832617 | ||||||
| chr8:28832651
|
G | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+2641C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832651 | ||||||
| chr8:28832674
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.488+2618T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832674 | ||||||
| chr8:28832768
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.488+2524A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832768 | ||||||
| chr8:28832935
|
C | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.488+2357G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832935 | ||||||
| chr8:28833065
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.488+2227T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833065 | ||||||
| chr8:28833101
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.488+2191C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833101 | ||||||
| chr8:28833109
|
C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.488+2183G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833109 | ||||||
| chr8:28833124
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+2168G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833124 | ||||||
| chr8:28833125
|
G | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0097 | 2 | HG01070.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.488+2167C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833125 | ||||||
| chr8:28833216
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.488+2076A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833216 | ||||||
| chr8:28833425
|
TC | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1866delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833425 | ||||||
| chr8:28833438
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.488+1854C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833438 | ||||||
| chr8:28833451
|
C | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0098 | 3 | NA18961.hp1 NA18966.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.488+1841G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833451 | ||||||
| chr8:28833480
|
T | C | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1812A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833480 | ||||||
| chr8:28833618
|
TCAAAAAC others(5): Show |
T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.488+1662_488+1673d others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833618 | ||||||
| chr8:28833620
|
A | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(115): Show | 120 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.488+1672T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833620 | ||||||
| chr8:28833638
|
A | C | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.488+1654T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833638 | ||||||
| chr8:28833642
|
ACAAAAAC | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1643_488+1649d others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833642 | ||||||
| chr8:28833650
|
C | A | 7 | a0001c0001t0003g0314a0001c0002t0003g0294a0001c0002t0003g0295others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+1642G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833650 | ||||||
| chr8:28833651
|
A | C | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1641T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833651 | ||||||
| chr8:28833678
|
G | GA | 10 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0272others(7): Show | 11 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+1613dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833678 | ||||||
| chr8:28834189
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.488+1103G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834189 | ||||||
| chr8:28834215
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.488+1077C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834215 | ||||||
| chr8:28834288
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1004G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834288 | ||||||
| chr8:28834321
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+971G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834321 | ||||||
| chr8:28834328
|
A | C | 1 | a0001c0001t0004g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488+964T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834328 | ||||||
| chr8:28834359
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0097 | 2 | HG01070.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.488+933G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834359 | ||||||
| chr8:28834546
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0304 | 2 | HG00558.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.488+746G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834546 | ||||||
| chr8:28834663
|
G | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+629C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834663 | ||||||
| chr8:28834676
|
G | GT | 66 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0025others(63): Show | 67 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.488+615dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834676 | ||||||
| chr8:28834676
|
GT | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(125): Show | 131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.488+615delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834676 | ||||||
| chr8:28834885
|
C | G | 1 | a0001c0001t0006g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.488+407G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834885 | ||||||
| chr8:28834968
|
C | T | 2 | a0001c0001t0003g0314a0001c0010t0003g0348 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.488+324G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834968 | ||||||
| chr8:28834971
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0060 | 2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.488+321G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834971 | ||||||
| chr8:28835134
|
T | C | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.488+158A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28835134 | ||||||
| chr8:28835155
|
C | G | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.488+137G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28835155 | ||||||
| chr8:28835266
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.488+26G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28835266 | ||||||
| chr8:28835421
|
T | G | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-43A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835421 | ||||||
| chr8:28835598
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.402-220T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835598 | ||||||
| chr8:28835667
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.402-289G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835667 | ||||||
| chr8:28835698
|
T | G | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.402-320A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835698 | ||||||
| chr8:28835797
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.402-419C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835797 | ||||||
| chr8:28835808
|
G | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-430C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835808 | ||||||
| chr8:28835873
|
A | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.402-495T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835873 | ||||||
| chr8:28836057
|
G | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402-679C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836057 | ||||||
| chr8:28836061
|
C | T | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.402-683G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836061 | ||||||
| chr8:28836195
|
A | C | 1 | a0001c0001t0001g0334 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.402-817T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836195 | ||||||
| chr8:28836250
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-872G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836250 | ||||||
| chr8:28836251
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.402-873C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836251 | ||||||
| chr8:28836289
|
G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.402-911C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836289 | ||||||
| chr8:28836294
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.402-916C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836294 | ||||||
| chr8:28836312
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 84 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.402-934C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836312 | ||||||
| chr8:28836358
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.402-980A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836358 | ||||||
| chr8:28836576
|
A | C | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(6): Show | 10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.401+1061T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836576 | ||||||
| chr8:28836698
|
G | A | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(8): Show | 12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.401+939C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836698 | ||||||
| chr8:28836727
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 108 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.401+910A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836727 | ||||||
| chr8:28836770
|
A | G | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.401+867T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836770 | ||||||
| chr8:28836857
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.401+780G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836857 | ||||||
| chr8:28836890
|
C | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+747G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836890 | ||||||
| chr8:28836906
|
C | T | 2 | a0001c0001t0001g0311a0001c0001t0001g0340 | 2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.401+731G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836906 | ||||||
| chr8:28837032
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.401+605G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837032 | ||||||
| chr8:28837248
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.401+389C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837248 | ||||||
| chr8:28837277
|
TTTC | T | 13 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.401+357_401+359del others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837277 | ||||||
| chr8:28837392
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0224 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.401+245C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837392 | ||||||
| chr8:28837437
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.401+200G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837437 | ||||||
| chr8:28837574
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401+63G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837574 | ||||||
| chr8:28837844
|
C | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(112): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.262-68G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837844 | ||||||
| chr8:28837860
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.262-84G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837860 | ||||||
| chr8:28837941
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.262-165T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837941 | ||||||
| chr8:28837966
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-190G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837966 | ||||||
| chr8:28838071
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.262-295G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838071 | ||||||
| chr8:28838163
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.262-387A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838163 | ||||||
| chr8:28838177
|
T | C | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-401A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838177 | ||||||
| chr8:28838191
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0045 | 2 | HG01074.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.262-415C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838191 | ||||||
| chr8:28838300
|
G | C | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-524C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838300 | ||||||
| chr8:28838355
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.262-579G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838355 | ||||||
| chr8:28838446
|
T | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0212 | 3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.262-670A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838446 | ||||||
| chr8:28838521
|
C | T | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(8): Show | 12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.262-745G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838521 | ||||||
| chr8:28838582
|
C | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0236a0001c0001t0001g0273others(1): Show | 4 | HG02071.hp2 HG02602.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-806G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838582 | ||||||
| chr8:28838878
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.262-1102C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838878 | ||||||
| chr8:28838892
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.262-1116G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838892 | ||||||
| chr8:28839042
|
G | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-1266C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839042 | ||||||
| chr8:28839131
|
G | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-1355C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839131 | ||||||
| chr8:28839203
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262-1427T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839203 | ||||||
| chr8:28839211
|
T | C | 9 | a0001c0001t0001g0344a0001c0001t0002g0350a0001c0001t0003g0314others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.262-1435A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839211 | ||||||
| chr8:28839279
|
T | G | 1 | a0001c0001t0001g0341 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.262-1503A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839279 | ||||||
| chr8:28839328
|
GT | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0088others(1): Show | 4 | HG02723.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1553delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839328 | ||||||
| chr8:28839345
|
C | T | 5 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1569G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839345 | ||||||
| chr8:28839346
|
A | G | 5 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1570T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839346 | ||||||
| chr8:28839472
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0025others(60): Show | 64 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.262-1696G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839472 | ||||||
| chr8:28839477
|
C | T | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-1701G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839477 | ||||||
| chr8:28839578
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(112): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.262-1802C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839578 | ||||||
| chr8:28839632
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0126others(2): Show | 5 | HG00597.hp1 NA18951.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-1856G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839632 | ||||||
| chr8:28839638
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.262-1862T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839638 | ||||||
| chr8:28839741
|
T | G | 3 | a0001c0001t0001g0105a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02145.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.262-1965A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839741 | ||||||
| chr8:28839821
|
C | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2045G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839821 | ||||||
| chr8:28839916
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.262-2140C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839916 | ||||||
| chr8:28839933
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00733.hp2 HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.262-2157A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839933 | ||||||
| chr8:28839955
|
C | A | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.262-2179G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839955 | ||||||
| chr8:28840029
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0025others(60): Show | 64 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.262-2253G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840029 | ||||||
| chr8:28840221
|
G | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2445C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840221 | ||||||
| chr8:28840270
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.262-2494T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840270 | ||||||
| chr8:28840294
|
G | A | 1 | a0001c0001t0006g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.262-2518C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840294 | ||||||
| chr8:28840384
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.262-2608A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840384 | ||||||
| chr8:28840475
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.262-2699T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840475 | ||||||
| chr8:28840505
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.262-2729A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840505 | ||||||
| chr8:28840506
|
G | A | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.262-2730C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840506 | ||||||
| chr8:28840581
|
G | T | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.262-2805C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840581 | ||||||
| chr8:28840665
|
C | A | 14 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0001g0169others(11): Show | 14 | HG00735.hp1 HG01975.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-2889G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840665 | ||||||
| chr8:28840685
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2909G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840685 | ||||||
| chr8:28840686
|
A | G | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2910T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840686 | ||||||
| chr8:28840731
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.262-2955C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840731 | ||||||
| chr8:28840734
|
C | T | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.262-2958G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840734 | ||||||
| chr8:28840797
|
T | TG | 43 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.262-3022dupC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840797 | ||||||
| chr8:28840844
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-3068A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840844 | ||||||
| chr8:28840959
|
T | TA | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0080others(6): Show | 9 | HG02109.hp2 HG02723.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-3184dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840959 | ||||||
| chr8:28840967
|
A | C | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.262-3191T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840967 | ||||||
| chr8:28840970
|
AG | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0328a0001c0001t0002g0164others(1): Show | 4 | HG02922.hp1 NA18522.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-3195delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840970 | ||||||
| chr8:28840971
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(303): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.262-3195C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840971 | ||||||
| chr8:28840988
|
A | AGCAGATC others(4): Show |
4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3213_262-3212i others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840988 | ||||||
| chr8:28840989
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3213G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840989 | ||||||
| chr8:28840992
|
A | G | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3216T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840992 | ||||||
| chr8:28841051
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.262-3275A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841051 | ||||||
| chr8:28841071
|
C | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.262-3295G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841071 | ||||||
| chr8:28841257
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.262-3481G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841257 | ||||||
| chr8:28841386
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.262-3610T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841386 | ||||||
| chr8:28841703
|
GA | G | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3928delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841703 | ||||||
| chr8:28841782
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0069 | 2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.262-4006G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841782 | ||||||
| chr8:28841866
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.262-4090C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841866 | ||||||
| chr8:28841867
|
C | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.262-4091G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841867 | ||||||
| chr8:28841944
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-4168G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841944 | ||||||
| chr8:28842065
|
G | C | 1 | a0001c0001t0001g0331 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.262-4289C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842065 | ||||||
| chr8:28842087
|
C | CA | 5 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG01884.hp2 HG01981.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-4312dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842087 | ||||||
| chr8:28842096
|
T | A | 1 | a0004c0004t0002g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.262-4320A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842096 | ||||||
| chr8:28842103
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0081 | 2 | HG01884.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.262-4327C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842103 | ||||||
| chr8:28842988
|
C | T | 5 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+3759G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842988 | ||||||
| chr8:28843027
|
G | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.261+3720C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843027 | ||||||
| chr8:28843037
|
T | G | 15 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(12): Show | 16 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.261+3710A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843037 | ||||||
| chr8:28843045
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.261+3702G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843045 | ||||||
| chr8:28843220
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+3527C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843220 | ||||||
| chr8:28843310
|
G | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0025others(57): Show | 61 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.261+3437C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843310 | ||||||
| chr8:28843348
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.261+3399C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843348 | ||||||
| chr8:28843636
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261+3111C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843636 | ||||||
| chr8:28843663
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.261+3084A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843663 | ||||||
| chr8:28843753
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261+2994C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843753 | ||||||
| chr8:28843834
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.261+2913G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843834 | ||||||
| chr8:28843835
|
A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.261+2912T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843835 | ||||||
| chr8:28843908
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.261+2839A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843908 | ||||||
| chr8:28844066
|
G | C | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(8): Show | 12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+2681C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844066 | ||||||
| chr8:28844077
|
G | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.261+2670C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844077 | ||||||
| chr8:28844105
|
A | G | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.261+2642T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844105 | ||||||
| chr8:28844147
|
C | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0025others(57): Show | 61 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.261+2600G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844147 | ||||||
| chr8:28844187
|
CTTTT | C | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(8): Show | 12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+2556_261+2559d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844187 | ||||||
| chr8:28844214
|
T | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0067others(116): Show | 121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.261+2533A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844214 | ||||||
| chr8:28844216
|
G | T | 22 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+2531C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844216 | ||||||
| chr8:28844368
|
C | G | 1 | a0001c0001t0001g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.261+2379G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844368 | ||||||
| chr8:28844564
|
G | A | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(8): Show | 12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+2183C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844564 | ||||||
| chr8:28844862
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.261+1885C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844862 | ||||||
| chr8:28845011
|
G | A | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1736C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845011 | ||||||
| chr8:28845095
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.261+1652G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845095 | ||||||
| chr8:28845282
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.261+1465G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845282 | ||||||
| chr8:28845426
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.261+1321C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845426 | ||||||
| chr8:28845525
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.261+1222A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845525 | ||||||
| chr8:28846039
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.261+708G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846039 | ||||||
| chr8:28846369
|
C | CTGGCACT others(10): Show |
1 | a0001c0001t0001g0253 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.261+377_261+378ins others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846369 | ||||||
| chr8:28846369
|
C | CTGGCATT others(10): Show |
238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.261+377_261+378ins others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846369 | ||||||
| chr8:28846369
|
C | CTGGCATT others(10): Show |
9 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+377_261+378ins others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846369 | ||||||
| chr8:28846393
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.261+354A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846393 | ||||||
| chr8:28846475
|
T | C | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.261+272A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846475 | ||||||
| chr8:28846912
|
C | G | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.199-103G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28846912 | ||||||
| chr8:28846984
|
G | T | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-175C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28846984 | ||||||
| chr8:28847063
|
C | A | 1 | a0001c0001t0004g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.199-254G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847063 | ||||||
| chr8:28847132
|
C | T | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.199-323G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847132 | ||||||
| chr8:28847268
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(1): Show | 4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-459A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847268 | ||||||
| chr8:28847329
|
C | T | 4 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0262others(1): Show | 4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-520G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847329 | ||||||
| chr8:28847454
|
TCCACCAC others(2): Show |
T | 3 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0191 | 3 | HG00735.hp1 HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.199-654_199-646del others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847454 | ||||||
| chr8:28847468
|
C | CACCACTA others(20): Show |
4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-686_199-660dup others(27): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847468 | ||||||
| chr8:28847603
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-794A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847603 | ||||||
| chr8:28847684
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.199-875T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847684 | ||||||
| chr8:28847794
|
G | C | 4 | a0001c0001t0001g0287a0001c0001t0001g0343a0001c0001t0002g0146others(1): Show | 4 | HG02809.hp2 HG06807.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-985C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847794 | ||||||
| chr8:28848186
|
A | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0073 | 3 | HG00639.hp1 HG01069.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.199-1377T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848186 | ||||||
| chr8:28848200
|
G | A | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-1391C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848200 | ||||||
| chr8:28848304
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.199-1495A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848304 | ||||||
| chr8:28848371
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.199-1562C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848371 | ||||||
| chr8:28848439
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 115 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.199-1630A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848439 | ||||||
| chr8:28848463
|
T | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.199-1654A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848463 | ||||||
| chr8:28848483
|
A | G | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1674T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848483 | ||||||
| chr8:28848548
|
T | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(111): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.198+1665A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848548 | ||||||
| chr8:28848555
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+1658C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848555 | ||||||
| chr8:28848645
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.198+1568A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848645 | ||||||
| chr8:28848750
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.198+1463A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848750 | ||||||
| chr8:28848758
|
C | T | 14 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+1455G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848758 | ||||||
| chr8:28848897
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | NA18945.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.198+1316C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848897 | ||||||
| chr8:28849046
|
G | C | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198+1167C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849046 | ||||||
| chr8:28849308
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198+905A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849308 | ||||||
| chr8:28849472
|
T | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.198+741A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849472 | ||||||
| chr8:28849528
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.198+685A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849528 | ||||||
| chr8:28849541
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198+672C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849541 | ||||||
| chr8:28849544
|
A | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0237a0001c0001t0001g0263 | 3 | NA18943.hp1 NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.198+669T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849544 | ||||||
| chr8:28849604
|
G | A | 1 | a0001c0001t0001g0341 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.198+609C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849604 | ||||||
| chr8:28849646
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.198+567G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849646 | ||||||
| chr8:28849663
|
G | A | 2 | a0001c0001t0003g0314a0001c0010t0003g0348 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+550C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849663 | ||||||
| chr8:28849984
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198+229A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849984 | ||||||
| chr8:28850053
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 115 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.198+160G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850053 | ||||||
| chr8:28850105
|
G | GA | 6 | a0001c0001t0001g0084a0001c0001t0001g0246a0001c0001t0002g0349others(3): Show | 6 | HG02572.hp2 HG02886.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+107dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850105 | ||||||
| chr8:28850105
|
GA | G | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(6): Show | 10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+107delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850105 | ||||||
| chr8:28850126
|
G | GTCACACT others(4): Show |
1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+76_198+86dupTA others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850126 | ||||||
| chr8:28850150
|
G | C | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+63C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850150 | ||||||
| chr8:28850408
|
T | TAAAAAAT others(323): Show |
1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-136_138-135ins others(330): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850408 | ||||||
| chr8:28850504
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0283 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.138-231T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850504 | ||||||
| chr8:28850531
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.138-258T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850531 | ||||||
| chr8:28850702
|
G | A | 19 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(16): Show | 19 | HG00597.hp1 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.138-429C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850702 | ||||||
| chr8:28850735
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.138-462T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850735 | ||||||
| chr8:28850836
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.138-563T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850836 | ||||||
| chr8:28850867
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.138-594G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850867 | ||||||
| chr8:28851129
|
AGGATTTC others(370): Show |
A | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138-1233_138-857de others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851129 | ||||||
| chr8:28851195
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138-922C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851195 | ||||||
| chr8:28851315
|
A | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.138-1042T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851315 | ||||||
| chr8:28851322
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.138-1049C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851322 | ||||||
| chr8:28851437
|
G | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0218a0001c0001t0001g0248 | 3 | NA18946.hp1 NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.138-1164C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851437 | ||||||
| chr8:28851586
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(108): Show | 113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.138-1313G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851586 | ||||||
| chr8:28851698
|
A | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG02886.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-1425T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851698 | ||||||
| chr8:28851863
|
T | G | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138-1590A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851863 | ||||||
| chr8:28851946
|
T | C | 4 | a0001c0001t0002g0349a0001c0001t0003g0309a0001c0001t0003g0310others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-1673A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851946 | ||||||
| chr8:28851958
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.138-1685G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851958 | ||||||
| chr8:28852028
|
G | A | 5 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-1755C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852028 | ||||||
| chr8:28852091
|
CGCTT | C | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(6): Show | 10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.138-1822_138-1819d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852091 | ||||||
| chr8:28852130
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.138-1857C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852130 | ||||||
| chr8:28852294
|
CT | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(126): Show | 132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.138-2022delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852294 | ||||||
| chr8:28852294
|
CTT | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(108): Show | 112 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.138-2023_138-2022d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852294 | ||||||
| chr8:28852328
|
A | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG01346.hp1 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-2055T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852328 | ||||||
| chr8:28852350
|
C | G | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138-2077G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852350 | ||||||
| chr8:28852993
|
T | C | 7 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-2720A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852993 | ||||||
| chr8:28852995
|
A | G | 7 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-2722T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852995 | ||||||
| chr8:28853023
|
A | G | 1 | a0001c0001t0006g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.138-2750T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853023 | ||||||
| chr8:28853073
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.138-2800G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853073 | ||||||
| chr8:28853266
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138-2993T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853266 | ||||||
| chr8:28853296
|
C | T | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.138-3023G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853296 | ||||||
| chr8:28853413
|
C | CAAA | 17 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(14): Show | 18 | HG01261.hp1 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.138-3143_138-3141d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853413 | ||||||
| chr8:28853527
|
C | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.138-3254G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853527 | ||||||
| chr8:28853675
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.138-3402G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853675 | ||||||
| chr8:28853692
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.138-3419T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853692 | ||||||
| chr8:28853770
|
CT | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0219others(6): Show | 10 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-3498delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853770 | ||||||
| chr8:28853777
|
T | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0087a0001c0001t0001g0094 | 3 | HG01243.hp1 HG01978.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.138-3504A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853777 | ||||||
| chr8:28853778
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.138-3505A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853778 | ||||||
| chr8:28853966
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.138-3693C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853966 | ||||||
| chr8:28854012
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 93 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.138-3739G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854012 | ||||||
| chr8:28854230
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138-3957C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854230 | ||||||
| chr8:28854394
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(105): Show | 110 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.138-4121C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854394 | ||||||
| chr8:28854493
|
A | C | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-4220T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854493 | ||||||
| chr8:28854578
|
T | C | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.138-4305A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854578 | ||||||
| chr8:28854897
|
T | C | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.137+4539A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854897 | ||||||
| chr8:28855084
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.137+4352T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855084 | ||||||
| chr8:28855087
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+4349G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855087 | ||||||
| chr8:28855097
|
C | A | 5 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+4339G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855097 | ||||||
| chr8:28855284
|
A | G | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.137+4152T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855284 | ||||||
| chr8:28855819
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.137+3617C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855819 | ||||||
| chr8:28855984
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0212 | 3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.137+3452T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855984 | ||||||
| chr8:28856097
|
G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+3339C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856097 | ||||||
| chr8:28856120
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.137+3316T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856120 | ||||||
| chr8:28856135
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.137+3301A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856135 | ||||||
| chr8:28856289
|
G | T | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.137+3147C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856289 | ||||||
| chr8:28856423
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.137+3013C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856423 | ||||||
| chr8:28856442
|
G | GTCTC | 8 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02280.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+2990_137+2993d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856442 | ||||||
| chr8:28856456
|
C | G | 1 | a0001c0001t0004g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137+2980G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856456 | ||||||
| chr8:28856476
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.137+2960G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856476 | ||||||
| chr8:28856661
|
C | T | 2 | a0001c0001t0002g0146a0004c0004t0002g0315 | 2 | HG02809.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.137+2775G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856661 | ||||||
| chr8:28856680
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.137+2756A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856680 | ||||||
| chr8:28857121
|
G | A | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.137+2315C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857121 | ||||||
| chr8:28857241
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.137+2195G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857241 | ||||||
| chr8:28857261
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0172others(7): Show | 11 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.137+2175T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857261 | ||||||
| chr8:28857360
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.137+2076A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857360 | ||||||
| chr8:28857484
|
G | GA | 3 | a0001c0001t0001g0102a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.137+1951dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857484 | ||||||
| chr8:28857560
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+1876T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857560 | ||||||
| chr8:28857622
|
A | G | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137+1814T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857622 | ||||||
| chr8:28857657
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1779A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857657 | ||||||
| chr8:28857676
|
T | A | 1 | a0001c0001t0001g0021 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.137+1760A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857676 | ||||||
| chr8:28857722
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1714T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857722 | ||||||
| chr8:28857836
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.137+1600G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857836 | ||||||
| chr8:28857935
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1501T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857935 | ||||||
| chr8:28858009
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(1): Show | 4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+1427G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858009 | ||||||
| chr8:28858079
|
G | A | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.137+1357C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858079 | ||||||
| chr8:28858115
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.137+1321T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858115 | ||||||
| chr8:28858155
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137+1281C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858155 | ||||||
| chr8:28858160
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1276C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858160 | ||||||
| chr8:28858592
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+844A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858592 | ||||||
| chr8:28858790
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.137+646G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858790 | ||||||
| chr8:28858974
|
T | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0190 | 2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.137+462A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858974 | ||||||
| chr8:28859021
|
T | TGAAAATA others(2874): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0308 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.137+414_137+415ins others(2881): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859021 | ||||||
| chr8:28859080
|
C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+356G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859080 | ||||||
| chr8:28859192
|
T | C | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(6): Show | 10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+244A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859192 | ||||||
| chr8:28859208
|
G | T | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137+228C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859208 | ||||||
| chr8:28859267
|
G | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(5): Show | 9 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+169C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859267 | ||||||
| chr8:28859423
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.137+13G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859423 | ||||||
| chr8:28859638
|
T | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-75A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28859638 | ||||||
| chr8:28859830
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.10-267A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28859830 | ||||||
| chr8:28859845
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-282G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28859845 | ||||||
| chr8:28860018
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.10-455G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860018 | ||||||
| chr8:28860021
|
GT | G | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(6): Show | 10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-459delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860021 | ||||||
| chr8:28860031
|
TTAAC | T | 3 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0003t0001g0351 | 3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.10-472_10-469delGT others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860031 | ||||||
| chr8:28860121
|
T | G | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.10-558A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860121 | ||||||
| chr8:28860147
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.10-584G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860147 | ||||||
| chr8:28860211
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0001g0131others(1): Show | 4 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-648T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860211 | ||||||
| chr8:28860300
|
A | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0328a0002c0006t0001g0325 | 3 | NA18962.hp1 NA19067.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.10-737T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860300 | ||||||
| chr8:28860323
|
C | A | 2 | a0001c0001t0003g0314a0001c0010t0003g0348 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-760G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860323 | ||||||
| chr8:28860475
|
C | CT | 6 | a0001c0001t0001g0072a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG00323.hp2 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-913dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860475 | ||||||
| chr8:28860664
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10-1101T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860664 | ||||||
| chr8:28860843
|
C | T | 3 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0305 | 3 | HG02630.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-1280G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860843 | ||||||
| chr8:28861120
|
A | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.10-1557T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861120 | ||||||
| chr8:28861313
|
C | A | 10 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(7): Show | 10 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-1750G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861313 | ||||||
| chr8:28861417
|
C | T | 1 | a0004c0004t0002g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.10-1854G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861417 | ||||||
| chr8:28861500
|
T | C | 2 | a0001c0001t0001g0352a0001c0001t0003g0314 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-1937A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861500 | ||||||
| chr8:28861527
|
G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.10-1964C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861527 | ||||||
| chr8:28861596
|
C | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.10-2033G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861596 | ||||||
| chr8:28861767
|
T | G | 24 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0170others(21): Show | 25 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-2204A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861767 | ||||||
| chr8:28861770
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.10-2207C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861770 | ||||||
| chr8:28862003
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.10-2440T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862003 | ||||||
| chr8:28862054
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-2491C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862054 | ||||||
| chr8:28862119
|
C | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-2556G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862119 | ||||||
| chr8:28862162
|
G | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-2599C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862162 | ||||||
| chr8:28862520
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-2957A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862520 | ||||||
| chr8:28862522
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.10-2959G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862522 | ||||||
| chr8:28862547
|
A | C | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-2984T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862547 | ||||||
| chr8:28862675
|
T | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3112A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862675 | ||||||
| chr8:28862793
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3230G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862793 | ||||||
| chr8:28862902
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-3339G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862902 | ||||||
| chr8:28863020
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG02165.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.10-3457T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863020 | ||||||
| chr8:28863174
|
A | AAGTGAAT others(270): Show |
1 | a0001c0001t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.10-3612_10-3611ins others(277): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863174 | ||||||
| chr8:28863212
|
T | A | 1 | a0001c0001t0001g0332 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10-3649A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863212 | ||||||
| chr8:28863530
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3967G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863530 | ||||||
| chr8:28863547
|
G | A | 24 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0170others(21): Show | 25 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-3984C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863547 | ||||||
| chr8:28863593
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10-4030G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863593 | ||||||
| chr8:28863610
|
T | C | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.10-4047A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863610 | ||||||
| chr8:28863611
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(110): Show | 115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.10-4048T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863611 | ||||||
| chr8:28863612
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-4049G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863612 | ||||||
| chr8:28863677
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-4114T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863677 | ||||||
| chr8:28863782
|
A | AAAAAAC | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0047others(9): Show | 12 | HG01167.hp1 HG01346.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.10-4225_10-4220dup others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863782 | ||||||
| chr8:28863856
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-4293C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863856 | ||||||
| chr8:28863937
|
T | C | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-4374A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863937 | ||||||
| chr8:28864076
|
C | T | 9 | a0001c0001t0001g0193a0001c0001t0001g0239a0001c0001t0001g0240others(6): Show | 9 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.10-4513G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864076 | ||||||
| chr8:28864080
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.10-4517A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864080 | ||||||
| chr8:28864164
|
G | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10-4601C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864164 | ||||||
| chr8:28864444
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-4881C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864444 | ||||||
| chr8:28864700
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 6 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-5137G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864700 | ||||||
| chr8:28864703
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-5140C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864703 | ||||||
| chr8:28864784
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.10-5221G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864784 | ||||||
| chr8:28864818
|
A | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5255T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864818 | ||||||
| chr8:28864972
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5409A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864972 | ||||||
| chr8:28864985
|
C | CA | 22 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 23 | HG01168.hp1 HG01346.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.10-5423dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864985 | ||||||
| chr8:28864995
|
A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG01175.hp1 HG01516.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5432T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864995 | ||||||
| chr8:28865249
|
A | T | 1 | a0001c0001t0001g0188 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.10-5686T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865249 | ||||||
| chr8:28865259
|
T | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(107): Show | 112 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.10-5696A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865259 | ||||||
| chr8:28865260
|
A | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5697T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865260 | ||||||
| chr8:28865472
|
T | TA | 8 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0150others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-5910dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865472 | ||||||
| chr8:28865539
|
T | C | 1 | a0001c0009t0001g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.10-5976A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865539 | ||||||
| chr8:28865818
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10-6255A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865818 | ||||||
| chr8:28866237
|
T | C | 5 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-6674A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866237 | ||||||
| chr8:28866243
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.10-6680A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866243 | ||||||
| chr8:28866244
|
A | G | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.10-6681T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866244 | ||||||
| chr8:28866283
|
A | G | 38 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(35): Show | 39 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.10-6720T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866283 | ||||||
| chr8:28866402
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.10-6839A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866402 | ||||||
| chr8:28866492
|
C | T | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.10-6929G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866492 | ||||||
| chr8:28866515
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-6952C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866515 | ||||||
| chr8:28866526
|
G | A | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10-6963C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866526 | ||||||
| chr8:28866568
|
T | G | 1 | a0001c0001t0001g0303 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.10-7005A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866568 | ||||||
| chr8:28866751
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.10-7188G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866751 | ||||||
| chr8:28866848
|
G | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-7285C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866848 | ||||||
| chr8:28866970
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0002g0350others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-7408_10-7407ins others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866970 | ||||||
| chr8:28866970
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0342 | 3 | HG02886.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.10-7408_10-7407ins others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866970 | ||||||
| chr8:28866970
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10-7408_10-7407ins others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866970 | ||||||
| chr8:28867030
|
T | C | 3 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0003t0001g0351 | 3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.10-7467A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867030 | ||||||
| chr8:28867052
|
C | T | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.10-7489G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867052 | ||||||
| chr8:28867264
|
A | AAAAC | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-7702_10-7701ins others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867264 | ||||||
| chr8:28867440
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10-7877A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867440 | ||||||
| chr8:28867450
|
A | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-7887T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867450 | ||||||
| chr8:28867459
|
C | T | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.10-7896G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867459 | ||||||
| chr8:28867526
|
G | A | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-7963C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867526 | ||||||
| chr8:28867531
|
T | TA | 7 | a0001c0001t0001g0077a0001c0001t0001g0092a0001c0001t0001g0144others(4): Show | 7 | HG01081.hp2 HG02300.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.10-7969dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867531 | ||||||
| chr8:28867531
|
TA | T | 9 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.10-7969delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867531 | ||||||
| chr8:28867532
|
A | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(108): Show | 113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.10-7969T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867532 | ||||||
| chr8:28867577
|
AACT | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.10-8017_10-8015del others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867577 | ||||||
| chr8:28867606
|
A | G | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-8043T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867606 | ||||||
| chr8:28867665
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10-8102T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867665 | ||||||
| chr8:28867677
|
G | A | 2 | a0001c0001t0001g0259a0001c0003t0001g0316 | 2 | HG02451.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.10-8114C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867677 | ||||||
| chr8:28867719
|
G | GT | 21 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(18): Show | 21 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.10-8157dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867719 | ||||||
| chr8:28867764
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.10-8201T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867764 | ||||||
| chr8:28867897
|
G | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.10-8334C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867897 | ||||||
| chr8:28867948
|
T | C | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-8385A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867948 | ||||||
| chr8:28868070
|
A | G | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0003g0309others(2): Show | 5 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-8507T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868070 | ||||||
| chr8:28868106
|
T | C | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0003g0309others(2): Show | 5 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-8543A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868106 | ||||||
| chr8:28868516
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0007g0041 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.10-8953C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868516 | ||||||
| chr8:28868556
|
G | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-8993C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868556 | ||||||
| chr8:28868795
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.10-9232A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868795 | ||||||
| chr8:28868840
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0344others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-9277A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868840 | ||||||
| chr8:28868841
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.10-9278C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868841 | ||||||
| chr8:28868869
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-9306C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868869 | ||||||
| chr8:28868881
|
CT | C | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0003g0309others(2): Show | 5 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-9319delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868881 | ||||||
| chr8:28868916
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.10-9353A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868916 | ||||||
| chr8:28868919
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.10-9356G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868919 | ||||||
| chr8:28868942
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0074others(112): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.10-9379A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868942 | ||||||
| chr8:28869012
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10-9449A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869012 | ||||||
| chr8:28869525
|
A | G | 10 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(7): Show | 10 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-9962T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869525 | ||||||
| chr8:28869543
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.10-9980T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869543 | ||||||
| chr8:28869644
|
A | G | 2 | a0001c0001t0003g0314a0001c0010t0003g0348 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-10081T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869644 | ||||||
| chr8:28869650
|
G | A | 9 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-10087C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869650 | ||||||
| chr8:28869997
|
T | C | 3 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0305 | 3 | HG02630.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-10434A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869997 | ||||||
| chr8:28870117
|
A | C | 1 | a0001c0001t0001g0333 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.10-10554T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870117 | ||||||
| chr8:28870135
|
C | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | NA18943.hp2 NA18959.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-10572G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870135 | ||||||
| chr8:28870145
|
T | C | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.10-10582A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870145 | ||||||
| chr8:28870319
|
A | AT | 124 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.10-10757dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870319 | ||||||
| chr8:28870319
|
A | ATT | 6 | a0001c0001t0001g0102a0001c0001t0001g0342a0001c0001t0001g0343others(3): Show | 6 | HG00738.hp2 HG01243.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-10758_10-10757d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870319 | ||||||
| chr8:28870349
|
CT | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0018others(77): Show | 81 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.10-10787delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | ||||||
| chr8:28870349
|
CTT | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.10-10788_10-10787d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | ||||||
| chr8:28870349
|
CTTT | C | 11 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0001g0282others(8): Show | 11 | HG01516.hp1 HG02109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.10-10789_10-10787d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | ||||||
| chr8:28870349
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0352a0001c0003t0001g0351 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.10-10799_10-10787d others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | ||||||
| chr8:28870357
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-10794A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870357 | ||||||
| chr8:28870358
|
T | C | 2 | a0001c0001t0001g0344a0001c0001t0002g0350 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.10-10795A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870358 | ||||||
| chr8:28870408
|
C | A | 2 | a0001c0001t0003g0314a0001c0010t0003g0348 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-10845G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870408 | ||||||
| chr8:28871151
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-11588T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871151 | ||||||
| chr8:28871161
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10-11598G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871161 | ||||||
| chr8:28871354
|
A | G | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.10-11791T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871354 | ||||||
| chr8:28871474
|
G | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.10-11911C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871474 | ||||||
| chr8:28871610
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.10-12047A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871610 | ||||||
| chr8:28871658
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-12095C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871658 | ||||||
| chr8:28871748
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0283 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.10-12185C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871748 | ||||||
| chr8:28871754
|
A | C | 2 | a0001c0002t0003g0294a0001c0002t0003g0297 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.10-12191T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871754 | ||||||
| chr8:28871763
|
T | C | 2 | a0001c0002t0003g0294a0001c0002t0003g0297 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.10-12200A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871763 | ||||||
| chr8:28871810
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0304 | 2 | HG00558.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.10-12247A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871810 | ||||||
| chr8:28871825
|
G | T | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.10-12262C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871825 | ||||||
| chr8:28871849
|
T | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.10-12286A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871849 | ||||||
| chr8:28871943
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0311a0001c0001t0001g0340 | 3 | HG00558.hp1 NA18993.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.10-12380T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871943 | ||||||
| chr8:28872060
|
C | G | 5 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-12497G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872060 | ||||||
| chr8:28872122
|
A | G | 3 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0002g0305 | 3 | HG02630.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-12559T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872122 | ||||||
| chr8:28872129
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.10-12566T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872129 | ||||||
| chr8:28872223
|
T | A | 1 | a0001c0001t0001g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.10-12660A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872223 | ||||||
| chr8:28872375
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10-12812A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872375 | ||||||
| chr8:28872408
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.10-12845C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872408 | ||||||
| chr8:28873007
|
T | G | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-13444A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873007 | ||||||
| chr8:28873051
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0087 | 2 | HG01243.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.10-13488C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873051 | ||||||
| chr8:28873101
|
TA | T | 4 | a0001c0002t0003g0294a0001c0002t0003g0295a0001c0002t0003g0296others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-13539delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873101 | ||||||
| chr8:28873714
|
T | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG01167.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.10-14151A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873714 | ||||||
| chr8:28873801
|
T | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.10-14238A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873801 | ||||||
| chr8:28873905
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.10-14342A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873905 | ||||||
| chr8:28873931
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.10-14368T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873931 | ||||||
| chr8:28873997
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.10-14434A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873997 | ||||||
| chr8:28874048
|
T | C | 1 | a0001c0001t0001g0298 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.10-14485A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874048 | ||||||
| chr8:28874100
|
ATTC | A | 3 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0003t0001g0351 | 3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.10-14540_10-14538d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874100 | ||||||
| chr8:28874289
|
G | GT | 6 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0086others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-14727dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874289 | ||||||
| chr8:28874322
|
C | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(5): Show | 9 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-14759G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874322 | ||||||
| chr8:28874450
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.10-14887G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874450 | ||||||
| chr8:28874451
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.10-14888C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874451 | ||||||
| chr8:28874606
|
A | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10-15043T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874606 | ||||||
| chr8:28874814
|
A | C | 1 | a0001c0001t0001g0211 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.9+15060T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874814 | ||||||
| chr8:28874890
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0163a0001c0001t0001g0167others(41): Show | 45 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.9+14984C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874890 | ||||||
| chr8:28875111
|
C | A | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+14763G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875111 | ||||||
| chr8:28875155
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0082others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+14719C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875155 | ||||||
| chr8:28875172
|
G | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0286 | 2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.9+14702C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875172 | ||||||
| chr8:28875249
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+14625C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875249 | ||||||
| chr8:28875289
|
C | CA | 13 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+14584dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875289 | ||||||
| chr8:28875371
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0137others(112): Show | 117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.9+14503A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875371 | ||||||
| chr8:28875432
|
G | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG01167.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+14442C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875432 | ||||||
| chr8:28875624
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.9+14250C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875624 | ||||||
| chr8:28875709
|
T | C | 1 | a0001c0001t0002g0262 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.9+14165A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875709 | ||||||
| chr8:28875827
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9+14047C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875827 | ||||||
| chr8:28875939
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG02056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.9+13935G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875939 | ||||||
| chr8:28876001
|
C | T | 4 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(1): Show | 4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+13873G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28876001 | ||||||
| chr8:28876098
|
C | T | 12 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02280.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.9+13776G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28876098 | ||||||
| chr8:28876569
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.9+13305A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28876569 | ||||||
| chr8:28877057
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0048others(1): Show | 5 | HG00140.hp2 HG01884.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+12817T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877057 | ||||||
| chr8:28877254
|
A | G | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.9+12620T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877254 | ||||||
| chr8:28877353
|
A | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01975.hp2 HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.9+12521T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877353 | ||||||
| chr8:28877534
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9+12340G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877534 | ||||||
| chr8:28877577
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.9+12297A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877577 | ||||||
| chr8:28877644
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.9+12230A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877644 | ||||||
| chr8:28877668
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.9+12206T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877668 | ||||||
| chr8:28877742
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.9+12132C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877742 | ||||||
| chr8:28877854
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+12020C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877854 | ||||||
| chr8:28877908
|
C | A | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(9): Show | 12 | HG02056.hp1 HG02809.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+11966G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877908 | ||||||
| chr8:28878208
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9+11666A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878208 | ||||||
| chr8:28878278
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0048others(1): Show | 5 | HG00140.hp2 HG01884.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+11596C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878278 | ||||||
| chr8:28878338
|
G | A | 5 | a0001c0001t0001g0352a0001c0001t0002g0312a0001c0001t0002g0349others(2): Show | 5 | HG02280.hp2 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+11536C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878338 | ||||||
| chr8:28878477
|
T | TA | 26 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0138others(23): Show | 27 | HG01175.hp2 HG01261.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.9+11396dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878477 | ||||||
| chr8:28878518
|
G | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+11356C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878518 | ||||||
| chr8:28878549
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+11325G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878549 | ||||||
| chr8:28878590
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.9+11284C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878590 | ||||||
| chr8:28878606
|
G | C | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.9+11268C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878606 | ||||||
| chr8:28878628
|
G | GT | 8 | a0001c0001t0001g0102a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01261.hp1 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+11245dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878628 | ||||||
| chr8:28878628
|
G | GTT | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(3): Show | 7 | HG02622.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+11244_9+11245dup others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878628 | ||||||
| chr8:28878641
|
T | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0272others(2): Show | 5 | HG00738.hp1 HG01070.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+11233A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878641 | ||||||
| chr8:28878641
|
T | TA | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(9): Show | 12 | HG02056.hp1 HG02809.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+11232dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878641 | ||||||
| chr8:28878642
|
A | T | 16 | a0001c0001t0001g0025a0001c0001t0001g0102a0001c0001t0001g0150others(13): Show | 16 | HG02572.hp2 HG02886.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.9+11232T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878642 | ||||||
| chr8:28878643
|
A | T | 4 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(1): Show | 4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+11231T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878643 | ||||||
| chr8:28878644
|
A | T | 4 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(1): Show | 4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+11230T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878644 | ||||||
| chr8:28878647
|
A | C | 6 | a0001c0001t0001g0353a0001c0002t0003g0294a0001c0002t0003g0295others(3): Show | 6 | HG00741.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.9+11227T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878647 | ||||||
| chr8:28878652
|
C | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9+11222G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878652 | ||||||
| chr8:28878670
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | NA18747.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.9+11204A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878670 | ||||||
| chr8:28878766
|
G | C | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0269others(5): Show | 8 | HG01358.hp1 HG01496.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+11108C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878766 | ||||||
| chr8:28878767
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0048others(1): Show | 5 | HG00140.hp2 HG01884.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+11107C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878767 | ||||||
| chr8:28878791
|
C | T | 10 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0171others(7): Show | 11 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+11083G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878791 | ||||||
| chr8:28878890
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.9+10984C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878890 | ||||||
| chr8:28878978
|
CA | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.9+10895delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878978 | ||||||
| chr8:28879045
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0283 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.9+10829C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879045 | ||||||
| chr8:28879250
|
CAGGAATG others(890): Show |
C | 1 | a0001c0001t0001g0306 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.9+9727_9+10623del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879250 | ||||||
| chr8:28879338
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9+10536A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879338 | ||||||
| chr8:28879399
|
G | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0137others(108): Show | 113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.9+10475C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879399 | ||||||
| chr8:28879606
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.9+10268A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879606 | ||||||
| chr8:28879712
|
G | C | 4 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02165.hp2 NA18963.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9+10162C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879712 | ||||||
| chr8:28879809
|
T | A | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(9): Show | 12 | HG02056.hp1 HG02809.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+10065A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879809 | ||||||
| chr8:28879823
|
C | A | 1 | a0002c0006t0001g0325 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.9+10051G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879823 | ||||||
| chr8:28879981
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9+9893A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879981 | ||||||
| chr8:28880034
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+9840A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880034 | ||||||
| chr8:28880131
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.9+9743T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880131 | ||||||
| chr8:28880225
|
G | GCTCTCC | 9 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0086others(6): Show | 9 | HG01109.hp1 HG02723.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+9643_9+9648dupGG others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | ||||||
| chr8:28880225
|
G | GCTCTCCC others(11): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0169 | 2 | HG02486.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.9+9631_9+9648dupGG others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | ||||||
| chr8:28880225
|
GCTCTCC | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 69 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.9+9643_9+9648delGG others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | ||||||
| chr8:28880225
|
GCTCTCCC others(5): Show |
G | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0029others(130): Show | 135 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.9+9637_9+9648delGG others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | ||||||
| chr8:28880225
|
GCTCTCCC others(11): Show |
G | 4 | a0001c0001t0001g0231a0001c0001t0002g0349a0001c0001t0002g0350others(1): Show | 4 | HG02280.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.9+9631_9+9648delGG others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | ||||||
| chr8:28880225
|
GCTCTCCC others(17): Show |
G | 4 | a0001c0001t0001g0102a0001c0001t0001g0172a0001c0001t0001g0342others(1): Show | 4 | HG02886.hp1 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+9625_9+9648delGG others(22): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | ||||||
| chr8:28880249
|
CCTCTCCC others(7): Show |
C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9611_9+9624delAG others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880249 | ||||||
| chr8:28880275
|
T | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9599A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880275 | ||||||
| chr8:28880277
|
T | G | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9597A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880277 | ||||||
| chr8:28880277
|
T | TCCCTCTC others(223): Show |
1 | a0001c0001t0001g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.9+9596_9+9597insGG others(228): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880277 | ||||||
| chr8:28880277
|
T | TCCCTCTC others(265): Show |
1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9+9596_9+9597insGG others(270): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880277 | ||||||
| chr8:28880278
|
C | G | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9596G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880278 | ||||||
| chr8:28880385
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.9+9489T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880385 | ||||||
| chr8:28880419
|
T | A | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+9455A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880419 | ||||||
| chr8:28880422
|
C | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02040.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.9+9452G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880422 | ||||||
| chr8:28880431
|
G | GT | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0018others(21): Show | 24 | HG00423.hp2 HG01175.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.9+9442dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880431 | ||||||
| chr8:28880469
|
C | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0163a0001c0001t0001g0167others(46): Show | 50 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.9+9405G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880469 | ||||||
| chr8:28880506
|
C | T | 7 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02572.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+9368G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880506 | ||||||
| chr8:28880521
|
G | A | 9 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+9353C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880521 | ||||||
| chr8:28880589
|
G | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0343 | 2 | HG01975.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.9+9285C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880589 | ||||||
| chr8:28880775
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 216 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.9+9099C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880775 | ||||||
| chr8:28880865
|
G | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.9+9009C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880865 | ||||||
| chr8:28880876
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+8998C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880876 | ||||||
| chr8:28881007
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.9+8867T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881007 | ||||||
| chr8:28881029
|
C | T | 3 | a0001c0001t0001g0344a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG02572.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9+8845G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881029 | ||||||
| chr8:28881035
|
AGAAGTGA others(33): Show |
A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.9+8799_9+8838delCC others(38): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881035 | ||||||
| chr8:28881055
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.9+8819A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881055 | ||||||
| chr8:28881100
|
C | T | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18944.hp1 NA18985.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.9+8774G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881100 | ||||||
| chr8:28881131
|
G | C | 4 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(1): Show | 4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+8743C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881131 | ||||||
| chr8:28881135
|
GC | G | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+8738delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881135 | ||||||
| chr8:28881173
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.9+8701C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881173 | ||||||
| chr8:28881175
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.9+8699C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881175 | ||||||
| chr8:28881206
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.9+8668A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881206 | ||||||
| chr8:28881215
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 223 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.9+8659G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881215 | ||||||
| chr8:28881219
|
TGCCCGGC others(42): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.9+8606_9+8654delGG others(47): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881219 | ||||||
| chr8:28881252
|
G | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9+8622C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881252 | ||||||
| chr8:28881285
|
AGTCCGGG others(269): Show |
A | 8 | a0001c0001t0001g0180a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 8 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+8313_9+8588del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881285 | ||||||
| chr8:28881316
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.9+8558G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881316 | ||||||
| chr8:28881330
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.9+8544C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881330 | ||||||
| chr8:28881363
|
G | A | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+8511C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881363 | ||||||
| chr8:28881398
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.9+8476G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881398 | ||||||
| chr8:28881416
|
C | T | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+8458G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881416 | ||||||
| chr8:28881444
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0283 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.9+8430G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881444 | ||||||
| chr8:28881444
|
C | T | 11 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(8): Show | 11 | HG02056.hp1 HG02809.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+8430G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881444 | ||||||
| chr8:28881464
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.9+8410G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881464 | ||||||
| chr8:28881465
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.9+8409G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881465 | ||||||
| chr8:28881476
|
A | AGGGGGGG others(42): Show |
1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.9+8397_9+8398insAC others(47): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | ||||||
| chr8:28881476
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0115 | 2 | HG02602.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.9+8398T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | ||||||
| chr8:28881476
|
AG | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.9+8397delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | ||||||
| chr8:28881476
|
AGGGGGGG others(43): Show |
A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0288others(1): Show | 4 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+8348_9+8397delAC others(48): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | ||||||
| chr8:28881477
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0339 | 2 | NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.9+8397C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881477 | ||||||
| chr8:28881588
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.9+8286G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881588 | ||||||
| chr8:28881602
|
AGCCGCCC others(120): Show |
A | 11 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(8): Show | 11 | HG02056.hp1 HG02809.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+8145_9+8271del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881602 | ||||||
| chr8:28881639
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.9+8235C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881639 | ||||||
| chr8:28881654
|
G | T | 3 | a0001c0001t0001g0344a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG02572.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9+8220C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881654 | ||||||
| chr8:28881666
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG02165.hp1 NA18954.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.9+8208G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881666 | ||||||
| chr8:28881674
|
C | CCGGCCAG others(42): Show |
1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+8199_9+8200insAC others(47): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | ||||||
| chr8:28881674
|
C | CCGGCCAG others(40): Show |
2 | a0001c0001t0002g0349a0001c0003t0001g0351 | 2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.9+8199_9+8200insAC others(45): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | ||||||
| chr8:28881674
|
C | CCGGCCAG others(39): Show |
1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+8199_9+8200insAC others(44): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | ||||||
| chr8:28881674
|
C | CCGGCCAG others(37): Show |
1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+8199_9+8200insAC others(42): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | ||||||
| chr8:28881700
|
AGGTGGGG others(120): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.9+8047_9+8173del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881700 | ||||||
| chr8:28881738
|
G | A | 1 | a0001c0001t0004g0002 | 2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+8136C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881738 | ||||||
| chr8:28881832
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9+8042C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881832 | ||||||
| chr8:28881834
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9+8040C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881834 | ||||||
| chr8:28881848
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9+8026C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881848 | ||||||
| chr8:28881851
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.9+8023G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881851 | ||||||
| chr8:28881872
|
A | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.9+8002T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881872 | ||||||
| chr8:28881873
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+8001C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881873 | ||||||
| chr8:28881892
|
C | T | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18944.hp1 NA18985.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.9+7982G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881892 | ||||||
| chr8:28881897
|
G | A | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.9+7977C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881897 | ||||||
| chr8:28881919
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+7955G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881919 | ||||||
| chr8:28881929
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0219others(7): Show | 11 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+7945G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881929 | ||||||
| chr8:28881985
|
T | C | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+7889A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881985 | ||||||
| chr8:28882088
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+7786G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882088 | ||||||
| chr8:28882109
|
C | A | 12 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02280.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.9+7765G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882109 | ||||||
| chr8:28882136
|
T | C | 3 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0003t0001g0351 | 3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.9+7738A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882136 | ||||||
| chr8:28882244
|
T | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+7630A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882244 | ||||||
| chr8:28882328
|
AGGCCG | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.9+7541_9+7545delCG others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882328 | ||||||
| chr8:28882334
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.9+7540G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882334 | ||||||
| chr8:28882459
|
A | T | 3 | a0001c0001t0001g0344a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG02572.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9+7415T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882459 | ||||||
| chr8:28882475
|
G | A | 12 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG02280.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.9+7399C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882475 | ||||||
| chr8:28882494
|
TA | T | 12 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0157others(9): Show | 13 | HG01261.hp1 HG02027.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+7379delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882494 | ||||||
| chr8:28882499
|
A | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 236 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.9+7375T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882499 | ||||||
| chr8:28882532
|
TA | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.9+7341delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882532 | ||||||
| chr8:28882547
|
A | G | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+7327T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882547 | ||||||
| chr8:28882548
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+7326C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882548 | ||||||
| chr8:28882548
|
GA | G | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(19): Show | 22 | HG00642.hp2 HG00735.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.9+7325delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882548 | ||||||
| chr8:28882549
|
A | G | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.9+7325T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882549 | ||||||
| chr8:28882605
|
G | A | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+7269C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882605 | ||||||
| chr8:28882610
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+7264T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882610 | ||||||
| chr8:28882955
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+6919G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882955 | ||||||
| chr8:28883225
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+6649A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883225 | ||||||
| chr8:28883510
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+6364G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883510 | ||||||
| chr8:28883678
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9+6196A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883678 | ||||||
| chr8:28883688
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9+6186G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883688 | ||||||
| chr8:28883710
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.9+6164C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883710 | ||||||
| chr8:28883732
|
ATC | A | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG00423.hp2 HG02071.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+6140_9+6141delGA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883732 | ||||||
| chr8:28884067
|
T | G | 66 | a0001c0001t0001g0005a0001c0001t0001g0163a0001c0001t0001g0167others(63): Show | 67 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.9+5807A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884067 | ||||||
| chr8:28884168
|
CT | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0129a0001c0001t0001g0130others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.9+5705delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTT | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(104): Show | 109 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.9+5704_9+5705delAA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(105): Show | 109 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.9+5703_9+5705delAA others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTTT | C | 10 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(7): Show | 10 | HG01070.hp2 HG01167.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+5702_9+5705delAA others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0308 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.9+5696_9+5705delAA others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0311a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG00558.hp1 HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.9+5695_9+5705delAA others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+5694_9+5705delAA others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0313a0001c0010t0003g0348 | 2 | HG02055.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.9+5693_9+5705delAA others(11): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884168
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.9+5690_9+5705delAA others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | ||||||
| chr8:28884217
|
G | A | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.9+5657C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884217 | ||||||
| chr8:28884627
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.9+5247G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884627 | ||||||
| chr8:28884768
|
G | A | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(9): Show | 12 | HG02056.hp1 HG02809.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+5106C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884768 | ||||||
| chr8:28884831
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+5043G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884831 | ||||||
| chr8:28885057
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.9+4817G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885057 | ||||||
| chr8:28885057
|
C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+4817G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885057 | ||||||
| chr8:28885109
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.9+4765A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885109 | ||||||
| chr8:28885247
|
C | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0004g0002others(5): Show | 9 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.9+4627G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885247 | ||||||
| chr8:28885390
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.9+4484G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885390 | ||||||
| chr8:28885624
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+4250T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885624 | ||||||
| chr8:28885645
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+4229A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885645 | ||||||
| chr8:28885726
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.9+4148T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885726 | ||||||
| chr8:28885910
|
A | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.9+3964T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885910 | ||||||
| chr8:28885964
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01975.hp2 HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.9+3910C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885964 | ||||||
| chr8:28886009
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.9+3865G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886009 | ||||||
| chr8:28886091
|
A | G | 4 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(1): Show | 4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3783T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886091 | ||||||
| chr8:28886208
|
TA | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 4 | HG02896.hp2 NA18963.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3665delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886208 | ||||||
| chr8:28886216
|
A | T | 9 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(6): Show | 9 | HG02056.hp1 NA18943.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.9+3658T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886216 | ||||||
| chr8:28886217
|
T | A | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.9+3657A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886217 | ||||||
| chr8:28886405
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0317a0001c0001t0001g0318others(22): Show | 26 | HG01109.hp2 HG03490.hp2 HG03927.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+3469C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886405 | ||||||
| chr8:28887369
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.9+2505C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28887369 | ||||||
| chr8:28887557
|
T | C | 1 | a0001c0001t0001g0341 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.9+2317A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28887557 | ||||||
| chr8:28887957
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0342 | 2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+1917C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28887957 | ||||||
| chr8:28888031
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.9+1843T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888031 | ||||||
| chr8:28888228
|
C | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.9+1646G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888228 | ||||||
| chr8:28888316
|
T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9+1558A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888316 | ||||||
| chr8:28888450
|
CGCG | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.9+1421_9+1423delCG others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888450 | ||||||
| chr8:28888456
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.9+1418C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888456 | ||||||
| chr8:28888507
|
G | A | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+1367C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888507 | ||||||
| chr8:28888694
|
G | A | 2 | a0001c0001t0001g0345a0001c0001t0001g0346 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+1180C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888694 | ||||||
| chr8:28888751
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+1123C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888751 | ||||||
| chr8:28888752
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+1122T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888752 | ||||||
| chr8:28888761
|
C | A | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+1113G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888761 | ||||||
| chr8:28888776
|
C | A | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.9+1098G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888776 | ||||||
| chr8:28888807
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.9+1067T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888807 | ||||||
| chr8:28889093
|
G | A | 5 | a0001c0001t0001g0352a0001c0001t0002g0349a0001c0001t0002g0350others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+781C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28889093 | ||||||
| chr8:28889285
|
A | G | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+589T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28889285 | ||||||
| chr8:28889391
|
G | C | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.9+483C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28889391 |