Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 115111 |
|---|---|
| ensemblid | ENSG00000147606.9 |
| hgncid | 14467 |
| symbol | SLC26A7 |
| name | solute carrier family 26 member 7 |
| refseq_nuc | NM_052832.4 |
| refseq_prot | NP_439897.1 |
| ensembl_nuc | ENST00000276609.8 |
| ensembl_prot | ENSP00000276609.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 91249319 |
| end | 91398155 |
| strand | + |
| ver | v1.2 |
| region | chr8:91249319-91398155 |
| region5000 | chr8:91244319-91403155 |
| regionname0 | SLC26A7_chr8_91249319_91398155 |
| regionname5000 | SLC26A7_chr8_91244319_91403155 |
| 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 | 1/0 | 656 | 199 | 72 | 55 | 44 | 6 | 21 | 28 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0002 | 0/1 | 656 | 7 | 3 | 1 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0003 | 0/0 | 656 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0004 | 0/0 | 656 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0005 | 0/0 | 656 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| 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 | 1/0 | 1971 | 148 | 46 | 40 | 41 | 5 | 15 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0002 | 0/0 | 1971 | 44 | 23 | 15 | 1 | 1 | 4 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0003 | 0/1 | 1971 | 7 | 3 | 1 | 0 | 2 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0004 | 0/0 | 1971 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0005 | 0/0 | 1971 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0006 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0007 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0008 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0009 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0010 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0011 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| c0012 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| 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 | 1/0 | 3267 | 142 | 39 | 43 | 36 | 5 | 18 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0002 | 0/0 | 3267 | 19 | 6 | 6 | 3 | 1 | 3 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0003 | 0/0 | 3267 | 7 | 7 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0004 | 0/0 | 3267 | 6 | 2 | 2 | 0 | 2 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0005 | 0/0 | 3267 | 5 | 4 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0006 | 0/0 | 3267 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0007 | 0/0 | 3267 | 3 | 0 | 0 | 3 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0008 | 0/0 | 3267 | 3 | 0 | 2 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0009 | 0/0 | 3267 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0010 | 0/0 | 3267 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0011 | 0/0 | 3266 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0012 | 0/0 | 3267 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0013 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0014 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0015 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0016 | 0/1 | 3267 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0017 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0018 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0019 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0020 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0021 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0022 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| t0023 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| 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 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| 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 | 1/0 | 1971 | 148 | 46 | 40 | 41 | 5 | 15 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002 | 0/0 | 1971 | 44 | 23 | 15 | 1 | 1 | 4 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0004 | 0/0 | 1971 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0005 | 0/0 | 1971 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0007 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0008 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0012 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0002c0003 | 0/1 | 1971 | 7 | 3 | 1 | 0 | 2 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0003c0006 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0003c0009 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0004c0011 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0005c0010 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5237 | 118 | 27 | 35 | 36 | 5 | 14 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0002 | 0/0 | 5237 | 7 | 4 | 2 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0003 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0004 | 0/0 | 5237 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0005 | 0/0 | 5237 | 4 | 3 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0007 | 0/0 | 5237 | 3 | 0 | 0 | 3 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0009 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0010 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0012 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0013 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0017 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0018 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0020 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0021 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0001t0023 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0001 | 0/0 | 5237 | 19 | 9 | 8 | 0 | 0 | 2 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0002 | 0/0 | 5237 | 9 | 2 | 4 | 1 | 1 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0003 | 0/0 | 5237 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0004 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0005 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0006 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0008 | 0/0 | 5237 | 3 | 0 | 2 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0009 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0012 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0015 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0002t0022 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0004t0002 | 0/0 | 5237 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0005t0006 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0007t0002 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0008t0001 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0001c0012t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0002c0003t0001 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0002c0003t0004 | 0/0 | 5237 | 3 | 0 | 1 | 0 | 2 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0002c0003t0016 | 0/1 | 5237 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0002c0003t0019 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0003c0006t0011 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0003c0009t0011 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0004c0011t0014 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| a0005c0010t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | copy fasta | chr8 | 91244319 | 91403155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0017g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0018g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0023g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0008g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0012g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0004t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0005t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0005t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0007t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0008t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0016g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0019g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0003c0006t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0003c0009t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0004c0011t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0005c0010t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0120 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0095 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00733 | hp2 | a0001 | c0002 | t0008 | g0190 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00735 | hp1 | a0001 | c0002 | t0012 | g0100 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0146 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0051 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01891 | hp1 | a0004 | c0011 | t0014 | g0022 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01934 | hp1 | a0001 | c0002 | t0008 | g0189 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01993 | hp1 | a0001 | c0001 | t0017 | g0192 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02055 | hp1 | a0003 | c0006 | t0011 | g0069 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0088 | EAS | CDX | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02257 | hp1 | a0001 | c0002 | t0006 | g0019 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0117 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0031 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0094 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0203 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0124 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02886 | hp2 | a0001 | c0001 | t0023 | g0104 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0092 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02970 | hp1 | a0001 | c0002 | t0009 | g0102 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02970 | hp2 | a0001 | c0005 | t0006 | g0109 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0136 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03130 | hp1 | a0001 | c0002 | t0022 | g0023 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0135 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0201 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03516 | hp1 | a0001 | c0002 | t0015 | g0024 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03927 | hp2 | a0001 | c0002 | t0008 | g0158 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03942 | hp2 | a0005 | c0010 | t0001 | g0074 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04184 | hp1 | a0001 | c0012 | t0001 | g0075 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04184 | hp2 | a0001 | c0007 | t0002 | g0195 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0206 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18947 | hp2 | a0001 | c0004 | t0002 | g0159 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18963 | hp1 | a0001 | c0004 | t0002 | g0144 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18966 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19006 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0204 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20752 | hp1 | a0002 | c0003 | t0004 | g0156 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0148 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20805 | hp1 | a0002 | c0003 | t0004 | g0157 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02486 | hp2 | a0002 | c0003 | t0019 | g0009 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG06807 | hp2 | a0001 | c0005 | t0006 | g0106 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20300 | hp2 | a0003 | c0009 | t0011 | g0143 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0016 | g0155 | REF | REF | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91318250
|
C | T | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.512C>T | p.Thr171Ile | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/19 | 720/5237 | 512/1971 | 171/656 | chr8 | 91318250 | ||
| chr8:91334295
|
A | G | 1 | a0002 | 7 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.643A>G | p.Ile215Val | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/19 | 851/5237 | 643/1971 | 215/656 | chr8 | 91334295 | ||
| chr8:91363504
|
A | T | 1 | a0005 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1454A>T | p.Glu485Val | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/19 | 1662/5237 | 1454/1971 | 485/656 | chr8 | 91363504 | ||
| chr8:91389374
|
A | C | 1 | a0003 | 2 | HG02055.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1712A>C | p.Tyr571Ser | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/19 | 1920/5237 | 1712/1971 | 571/656 | chr8 | 91389374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91295565
|
C | T | 1 | a0001c0012 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.339C>T | p.Asn113Asn | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/19 | 547/5237 | 339/1971 | 113/656 | chr8 | 91295565 | ||
| chr8:91351872
|
T | C | 3 | a0001c0002a0001c0004a0003c0006 | 47 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(44): Show |
synonymous_variant | LOW | c.1203T>C | p.Leu401Leu | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/19 | 1411/5237 | 1203/1971 | 401/656 | chr8 | 91351872 | ||
| chr8:91362412
|
G | A | 1 | a0001c0007 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1374G>A | p.Leu458Leu | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/19 | 1582/5237 | 1374/1971 | 458/656 | chr8 | 91362412 | ||
| chr8:91393841
|
C | T | 1 | a0001c0004 | 2 | NA18947.hp2 NA18963.hp1 |
synonymous_variant | LOW | c.1821C>T | p.Ala607Ala | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 17/19 | 2029/5237 | 1821/1971 | 607/656 | chr8 | 91393841 | ||
| chr8:91394003
|
G | A | 1 | a0001c0005 | 2 | HG02970.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.1899G>A | p.Ser633Ser | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/19 | 2107/5237 | 1899/1971 | 633/656 | chr8 | 91394003 | ||
| chr8:91394012
|
T | C | 1 | a0001c0008 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1908T>C | p.Ala636Ala | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/19 | 2116/5237 | 1908/1971 | 636/656 | chr8 | 91394012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91395105
|
T | C | 2 | a0003c0006t0011a0003c0009t0011 | 2 | HG02055.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 8 | chr8 | 91395105 | |||||
| chr8:91395218
|
C | T | 7 | a0001c0001t0002a0001c0001t0023a0001c0002t0002others(4): Show | 22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*121C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 121 | chr8 | 91395218 | |||||
| chr8:91395247
|
G | A | 1 | a0001c0001t0013 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 150 | chr8 | 91395247 | |||||
| chr8:91395296
|
G | A | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(11): Show | 37 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*199G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 199 | chr8 | 91395296 | |||||
| chr8:91395471
|
G | T | 7 | a0001c0001t0002a0001c0001t0023a0001c0002t0002others(4): Show | 22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*374G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 374 | chr8 | 91395471 | |||||
| chr8:91395562
|
C | T | 3 | a0001c0001t0012a0001c0002t0012a0001c0002t0022 | 3 | HG00735.hp1 HG02572.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*465C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 465 | chr8 | 91395562 | |||||
| chr8:91395677
|
C | T | 1 | a0001c0001t0021 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 580 | chr8 | 91395677 | |||||
| chr8:91395883
|
A | G | 1 | a0001c0001t0010 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*786A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 786 | chr8 | 91395883 | |||||
| chr8:91395936
|
A | G | 1 | a0001c0001t0020 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 839 | chr8 | 91395936 | |||||
| chr8:91396017
|
A | G | 2 | a0001c0001t0009a0001c0002t0009 | 3 | HG02970.hp1 HG03041.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*920A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 920 | chr8 | 91396017 | |||||
| chr8:91396102
|
T | G | 7 | a0001c0001t0002a0001c0001t0023a0001c0002t0002others(4): Show | 22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1005T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1005 | chr8 | 91396102 | |||||
| chr8:91396110
|
A | G | 1 | a0001c0002t0015 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1013 | chr8 | 91396110 | |||||
| chr8:91396226
|
T | C | 2 | a0001c0001t0005a0001c0002t0005 | 5 | HG01109.hp2 HG01884.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1129T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1129 | chr8 | 91396226 | |||||
| chr8:91396755
|
G | C | 1 | a0001c0002t0022 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1658 | chr8 | 91396755 | |||||
| chr8:91396819
|
C | T | 9 | a0001c0001t0002a0001c0001t0018a0001c0001t0023others(6): Show | 24 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1722C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1722 | chr8 | 91396819 | |||||
| chr8:91396842
|
T | C | 7 | a0001c0001t0002a0001c0001t0023a0001c0002t0002others(4): Show | 22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1745T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1745 | chr8 | 91396842 | |||||
| chr8:91396867
|
G | A | 3 | a0001c0001t0023a0003c0006t0011a0003c0009t0011 | 3 | HG02055.hp1 HG02886.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1770 | chr8 | 91396867 | |||||
| chr8:91396910
|
G | A | 4 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(1): Show | 19 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1813G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1813 | chr8 | 91396910 | |||||
| chr8:91397053
|
G | A | 1 | a0001c0001t0007 | 3 | HG00558.hp2 NA19006.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1956G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1956 | chr8 | 91397053 | |||||
| chr8:91397193
|
T | C | 1 | a0001c0001t0018 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2096 | chr8 | 91397193 | |||||
| chr8:91397200
|
T | G | 1 | a0001c0002t0008 | 3 | HG00733.hp2 HG01934.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2103T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2103 | chr8 | 91397200 | |||||
| chr8:91397220
|
G | A | 3 | a0001c0001t0003a0001c0002t0003a0004c0011t0014 | 8 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2123G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2123 | chr8 | 91397220 | |||||
| chr8:91397271
|
GT | G | 2 | a0003c0006t0011a0003c0009t0011 | 2 | HG02055.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2175delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2175 | chr8 | 91397271 | |||||
| chr8:91397311
|
G | A | 3 | a0001c0001t0003a0001c0002t0003a0004c0011t0014 | 8 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2214G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2214 | chr8 | 91397311 | |||||
| chr8:91397313
|
C | T | 1 | a0004c0011t0014 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2216 | chr8 | 91397313 | |||||
| chr8:91397469
|
G | A | 7 | a0001c0001t0002a0001c0001t0023a0001c0002t0002others(4): Show | 22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2372G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2372 | chr8 | 91397469 | |||||
| chr8:91397527
|
G | T | 1 | a0001c0001t0017 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2430 | chr8 | 91397527 | |||||
| chr8:91397841
|
A | G | 2 | a0001c0001t0003a0001c0002t0003 | 7 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2744A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2744 | chr8 | 91397841 | |||||
| chr8:91397861
|
A | G | 7 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(4): Show | 15 | HG00642.hp1 HG00738.hp1 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2764A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2764 | chr8 | 91397861 | |||||
| chr8:91397962
|
A | C | 2 | a0001c0002t0006a0001c0005t0006 | 4 | HG02257.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2865A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2865 | chr8 | 91397962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91249477
|
A | G | 9 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(6): Show | 9 | HG02257.hp2 HG02809.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-113-62A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 1/18 | chr8 | 91249477 | ||||||
| chr8:91249495
|
A | ATC | 3 | a0001c0001t0005g0004a0001c0001t0007g0005a0001c0001t0007g0006 | 3 | HG01109.hp2 NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-113-26_-113-25dup others(2): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 91249495 | |||||
| chr8:91250057
|
T | G | 2 | a0001c0001t0001g0008a0001c0001t0002g0007 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.193+213T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91250057 | ||||||
| chr8:91250656
|
T | G | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.193+812T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91250656 | ||||||
| chr8:91250933
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0196a0001c0002t0001g0197others(1): Show | 5 | HG00735.hp2 HG00738.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+1089C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91250933 | ||||||
| chr8:91251047
|
AT | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(131): Show | 136 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.193+1213delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91251047 | |||||
| chr8:91251253
|
A | G | 16 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0001g0115others(13): Show | 16 | HG00558.hp2 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+1409A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251253 | ||||||
| chr8:91251455
|
A | T | 1 | a0001c0001t0009g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193+1611A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251455 | ||||||
| chr8:91251672
|
C | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+1828C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251672 | ||||||
| chr8:91251804
|
C | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0030others(87): Show | 92 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.193+1960C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251804 | ||||||
| chr8:91252102
|
T | C | 1 | a0001c0002t0002g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193+2258T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252102 | ||||||
| chr8:91252155
|
T | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(152): Show | 158 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.193+2311T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252155 | ||||||
| chr8:91252378
|
C | A | 2 | a0001c0001t0018g0124a0001c0002t0003g0125 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.193+2534C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252378 | ||||||
| chr8:91252552
|
G | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0194others(6): Show | 9 | HG00558.hp2 HG01123.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+2708G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252552 | ||||||
| chr8:91252735
|
A | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+2891A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252735 | ||||||
| chr8:91252940
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.193+3096A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252940 | ||||||
| chr8:91253295
|
C | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(49): Show | 52 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.193+3451C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253295 | ||||||
| chr8:91253400
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.193+3556T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253400 | ||||||
| chr8:91253405
|
C | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3561C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253405 | ||||||
| chr8:91253410
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0025others(74): Show | 80 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.193+3566A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253410 | ||||||
| chr8:91253464
|
C | T | 4 | a0001c0001t0001g0018a0001c0002t0015g0024a0001c0002t0022g0023others(1): Show | 4 | HG01261.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+3620C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253464 | ||||||
| chr8:91253504
|
A | G | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+3660A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253504 | ||||||
| chr8:91253755
|
C | T | 11 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+3911C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253755 | ||||||
| chr8:91254079
|
T | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0005g0004others(6): Show | 9 | HG01070.hp2 HG01109.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+4235T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254079 | ||||||
| chr8:91254250
|
G | A | 2 | a0001c0001t0001g0145a0001c0004t0002g0144 | 2 | NA18963.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.193+4406G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254250 | ||||||
| chr8:91254576
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+4732T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254576 | ||||||
| chr8:91254683
|
G | A | 2 | a0001c0001t0001g0119a0001c0002t0002g0121 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.193+4839G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254683 | ||||||
| chr8:91254735
|
T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+4891T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254735 | ||||||
| chr8:91255055
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.193+5211A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255055 | ||||||
| chr8:91255190
|
T | C | 16 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(13): Show | 16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+5346T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255190 | ||||||
| chr8:91255263
|
A | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+5419A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255263 | ||||||
| chr8:91255329
|
A | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+5485A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255329 | ||||||
| chr8:91255529
|
C | G | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+5685C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255529 | ||||||
| chr8:91255581
|
A | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+5737A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255581 | ||||||
| chr8:91255803
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+5959A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255803 | ||||||
| chr8:91255982
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193+6138T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255982 | ||||||
| chr8:91256150
|
C | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0072 | 3 | HG03195.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.193+6306C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256150 | ||||||
| chr8:91256304
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+6460C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256304 | ||||||
| chr8:91256397
|
A | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+6553A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256397 | ||||||
| chr8:91256676
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.193+6832G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256676 | ||||||
| chr8:91257167
|
A | G | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+7323A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257167 | ||||||
| chr8:91257595
|
C | A | 3 | a0001c0001t0001g0111a0001c0002t0001g0110a0001c0002t0001g0112 | 3 | HG01081.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.193+7751C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257595 | ||||||
| chr8:91257626
|
A | T | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193+7782A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257626 | ||||||
| chr8:91257635
|
A | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0115others(9): Show | 13 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.193+7791A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257635 | ||||||
| chr8:91257729
|
G | C | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193+7885G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257729 | ||||||
| chr8:91257928
|
A | G | 2 | a0001c0001t0001g0071a0001c0002t0002g0070 | 2 | NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.193+8084A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257928 | ||||||
| chr8:91257935
|
C | T | 2 | a0001c0001t0001g0137a0003c0006t0011g0069 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.193+8091C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257935 | ||||||
| chr8:91258007
|
A | G | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+8163A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258007 | ||||||
| chr8:91258428
|
G | C | 2 | a0001c0001t0001g0191a0001c0001t0017g0192 | 2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.193+8584G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258428 | ||||||
| chr8:91258637
|
T | C | 2 | a0001c0001t0001g0119a0001c0002t0002g0121 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.193+8793T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258637 | ||||||
| chr8:91258662
|
TAA | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+8819_193+8820d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258662 | ||||||
| chr8:91258682
|
C | G | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+8838C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258682 | ||||||
| chr8:91258963
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.193+9119C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258963 | ||||||
| chr8:91258964
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+9120G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258964 | ||||||
| chr8:91259281
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.193+9437C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259281 | ||||||
| chr8:91259354
|
G | A | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+9510G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259354 | ||||||
| chr8:91259364
|
G | T | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+9520G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259364 | ||||||
| chr8:91259481
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+9637G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259481 | ||||||
| chr8:91259635
|
C | T | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.193+9791C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259635 | ||||||
| chr8:91259739
|
A | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+9895A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259739 | ||||||
| chr8:91259739
|
A | T | 22 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.193+9895A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259739 | ||||||
| chr8:91259749
|
A | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+9905A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259749 | ||||||
| chr8:91259767
|
G | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193+9923G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259767 | ||||||
| chr8:91259895
|
T | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.193+10051T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259895 | ||||||
| chr8:91259909
|
T | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.193+10065T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259909 | ||||||
| chr8:91260046
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193+10202T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260046 | ||||||
| chr8:91260156
|
A | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0002t0002g0070 | 3 | HG02523.hp2 NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.193+10312A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260156 | ||||||
| chr8:91260318
|
G | A | 60 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(57): Show | 60 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.193+10474G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260318 | ||||||
| chr8:91260437
|
C | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+10593C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260437 | ||||||
| chr8:91260973
|
C | T | 3 | a0001c0001t0010g0092a0001c0001t0010g0093a0001c0001t0010g0094 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.193+11129C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260973 | ||||||
| chr8:91261088
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0009g0201 | 3 | HG02896.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.193+11244G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261088 | ||||||
| chr8:91261108
|
T | G | 1 | a0005c0010t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.193+11264T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261108 | ||||||
| chr8:91261432
|
G | C | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+11588G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261432 | ||||||
| chr8:91261485
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.193+11641G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261485 | ||||||
| chr8:91261568
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.193+11724G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261568 | ||||||
| chr8:91261734
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.193+11890G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261734 | ||||||
| chr8:91262002
|
C | T | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+12158C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262002 | ||||||
| chr8:91262138
|
C | T | 2 | a0001c0001t0001g0071a0001c0002t0002g0070 | 2 | NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.193+12294C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262138 | ||||||
| chr8:91262451
|
A | G | 16 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(13): Show | 16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+12607A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262451 | ||||||
| chr8:91262554
|
C | G | 8 | a0001c0001t0001g0010a0001c0001t0005g0108a0001c0001t0018g0124others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+12710C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262554 | ||||||
| chr8:91262892
|
T | A | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+13048T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262892 | ||||||
| chr8:91262919
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+13075C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262919 | ||||||
| chr8:91263041
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193+13197C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263041 | ||||||
| chr8:91263068
|
C | T | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193+13224C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263068 | ||||||
| chr8:91263234
|
A | T | 5 | a0001c0001t0001g0039a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00558.hp1 NA18960.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+13390A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263234 | ||||||
| chr8:91263540
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+13696C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263540 | ||||||
| chr8:91263576
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.193+13732G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263576 | ||||||
| chr8:91263644
|
C | T | 22 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.193+13800C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263644 | ||||||
| chr8:91263680
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.193+13836G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263680 | ||||||
| chr8:91263966
|
AT | A | 22 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.193+14131delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91263966 | |||||
| chr8:91264606
|
C | T | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+14762C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264606 | ||||||
| chr8:91264657
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.193+14813G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264657 | ||||||
| chr8:91264722
|
G | A | 3 | a0001c0001t0004g0202a0001c0001t0012g0117a0001c0002t0004g0203 | 3 | HG02257.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.193+14878G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264722 | ||||||
| chr8:91264748
|
A | T | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+14904A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264748 | ||||||
| chr8:91264995
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.193+15151C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264995 | ||||||
| chr8:91265154
|
G | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+15310G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265154 | ||||||
| chr8:91265377
|
C | T | 4 | a0001c0001t0001g0030a0001c0002t0015g0024a0001c0002t0022g0023others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+15533C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265377 | ||||||
| chr8:91265537
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(59): Show | 63 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.193+15693T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265537 | ||||||
| chr8:91265724
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193+15880T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265724 | ||||||
| chr8:91265740
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+15896T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265740 | ||||||
| chr8:91265761
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.193+15917G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265761 | ||||||
| chr8:91265893
|
T | G | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193+16049T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265893 | ||||||
| chr8:91266161
|
A | T | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193+16317A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266161 | ||||||
| chr8:91266178
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193+16334C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266178 | ||||||
| chr8:91266219
|
G | A | 3 | a0001c0001t0005g0004a0001c0002t0002g0046a0001c0002t0002g0047 | 3 | HG01070.hp2 HG01109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.193+16375G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266219 | ||||||
| chr8:91266327
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+16483G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266327 | ||||||
| chr8:91266446
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.193+16602A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266446 | ||||||
| chr8:91267055
|
T | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+17211T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267055 | ||||||
| chr8:91267060
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+17216A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267060 | ||||||
| chr8:91267070
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(157): Show | 163 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.193+17226T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267070 | ||||||
| chr8:91267105
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+17261T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267105 | ||||||
| chr8:91267207
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.193+17363T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267207 | ||||||
| chr8:91267271
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+17427T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267271 | ||||||
| chr8:91267283
|
G | A | 1 | a0001c0012t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193+17439G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267283 | ||||||
| chr8:91267360
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+17516A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267360 | ||||||
| chr8:91267509
|
T | C | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+17665T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267509 | ||||||
| chr8:91267660
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(147): Show | 153 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.193+17816A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267660 | ||||||
| chr8:91267681
|
T | C | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.193+17837T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267681 | ||||||
| chr8:91267910
|
C | T | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.193+18066C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267910 | ||||||
| chr8:91268335
|
T | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+18491T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268335 | ||||||
| chr8:91268434
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.193+18590T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268434 | ||||||
| chr8:91268560
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.193+18716A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268560 | ||||||
| chr8:91268678
|
T | A | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+18834T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268678 | ||||||
| chr8:91268684
|
G | C | 1 | a0001c0001t0012g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.193+18840G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268684 | ||||||
| chr8:91268885
|
T | A | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+19041T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268885 | ||||||
| chr8:91268943
|
CA | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(149): Show | 155 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.193+19109delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91268943 | |||||
| chr8:91269027
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193+19183T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269027 | ||||||
| chr8:91269223
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.193+19379A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269223 | ||||||
| chr8:91269294
|
C | CAG | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+19451_193+1945 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91269294 | |||||
| chr8:91269407
|
G | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+19563G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269407 | ||||||
| chr8:91269507
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-19629A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269507 | ||||||
| chr8:91269707
|
T | A | 5 | a0001c0001t0001g0101a0001c0001t0005g0099a0001c0002t0001g0103others(2): Show | 5 | HG00735.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-19429T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269707 | ||||||
| chr8:91269906
|
A | AT | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-19225dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91269906 | |||||
| chr8:91269937
|
A | G | 4 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-19199A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269937 | ||||||
| chr8:91269947
|
T | C | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.194-19189T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269947 | ||||||
| chr8:91270080
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-19056A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270080 | ||||||
| chr8:91270087
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-19049T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270087 | ||||||
| chr8:91270123
|
T | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-19013T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270123 | ||||||
| chr8:91270261
|
T | C | 3 | a0001c0002t0015g0024a0001c0002t0022g0023a0004c0011t0014g0022 | 3 | HG01891.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194-18875T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270261 | ||||||
| chr8:91270271
|
G | A | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-18865G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270271 | ||||||
| chr8:91270372
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.194-18764G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270372 | ||||||
| chr8:91270405
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-18731A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270405 | ||||||
| chr8:91270525
|
T | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-18611T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270525 | ||||||
| chr8:91270682
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.194-18454A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270682 | ||||||
| chr8:91270706
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.194-18430T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270706 | ||||||
| chr8:91271003
|
A | G | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-18133A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271003 | ||||||
| chr8:91271103
|
G | A | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-18033G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271103 | ||||||
| chr8:91271167
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.194-17969T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271167 | ||||||
| chr8:91271238
|
G | T | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-17898G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271238 | ||||||
| chr8:91271371
|
G | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-17765G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271371 | ||||||
| chr8:91271402
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17734C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271402 | ||||||
| chr8:91271590
|
C | CT | 16 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0050others(13): Show | 17 | HG00438.hp1 HG00609.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-17524dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | |||||
| chr8:91271590
|
C | CTT | 6 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0009g0201others(3): Show | 6 | HG02572.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-17525_194-1752 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | |||||
| chr8:91271590
|
CTTT | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17526_194-1752 others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | |||||
| chr8:91271590
|
CTTTT | C | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-17527_194-1752 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | |||||
| chr8:91271626
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17510G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271626 | ||||||
| chr8:91271719
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-17417C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271719 | ||||||
| chr8:91271796
|
G | A | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.194-17340G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271796 | ||||||
| chr8:91271828
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.194-17308T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271828 | ||||||
| chr8:91271978
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17158G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271978 | ||||||
| chr8:91272011
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17125A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272011 | ||||||
| chr8:91272195
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-16941T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272195 | ||||||
| chr8:91272365
|
A | G | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-16771A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272365 | ||||||
| chr8:91272537
|
C | T | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-16599C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272537 | ||||||
| chr8:91272766
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.194-16370T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272766 | ||||||
| chr8:91272949
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.194-16187T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272949 | ||||||
| chr8:91272981
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-16155C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272981 | ||||||
| chr8:91273018
|
G | A | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-16118G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273018 | ||||||
| chr8:91273166
|
A | T | 6 | a0001c0001t0001g0013a0001c0002t0003g0011a0001c0002t0003g0017others(3): Show | 6 | HG02622.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-15970A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273166 | ||||||
| chr8:91273193
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.194-15943G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273193 | ||||||
| chr8:91273207
|
G | A | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-15929G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273207 | ||||||
| chr8:91273494
|
A | G | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-15642A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273494 | ||||||
| chr8:91273675
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-15461C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273675 | ||||||
| chr8:91273999
|
T | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-15137T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273999 | ||||||
| chr8:91274003
|
G | A | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-15133G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274003 | ||||||
| chr8:91274017
|
G | A | 22 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-15119G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274017 | ||||||
| chr8:91274060
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-15076T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274060 | ||||||
| chr8:91274155
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.194-14981G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274155 | ||||||
| chr8:91274265
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.194-14871G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274265 | ||||||
| chr8:91274354
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0003g0133 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-14782T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274354 | ||||||
| chr8:91274442
|
G | A | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-14694G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274442 | ||||||
| chr8:91274470
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-14666G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274470 | ||||||
| chr8:91274900
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-14236A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274900 | ||||||
| chr8:91275037
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.194-14099G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275037 | ||||||
| chr8:91275182
|
C | T | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.194-13954C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275182 | ||||||
| chr8:91275189
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.194-13947T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275189 | ||||||
| chr8:91275282
|
A | G | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194-13854A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275282 | ||||||
| chr8:91275416
|
C | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-13720C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275416 | ||||||
| chr8:91275556
|
T | A | 1 | a0001c0002t0001g0080 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.194-13580T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275556 | ||||||
| chr8:91275618
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0091others(1): Show | 4 | HG00733.hp1 HG01243.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13518C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275618 | ||||||
| chr8:91275679
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-13457A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275679 | ||||||
| chr8:91275688
|
G | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-13448G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275688 | ||||||
| chr8:91275737
|
C | T | 4 | a0001c0001t0001g0030a0001c0002t0015g0024a0001c0002t0022g0023others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13399C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275737 | ||||||
| chr8:91275792
|
G | A | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-13344G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275792 | ||||||
| chr8:91275875
|
A | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-13261A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275875 | ||||||
| chr8:91275881
|
G | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0002c0003t0004g0095others(3): Show | 6 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-13255G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275881 | ||||||
| chr8:91275908
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.194-13228T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275908 | ||||||
| chr8:91275965
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-13171C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275965 | ||||||
| chr8:91276005
|
T | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-13131T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276005 | ||||||
| chr8:91276074
|
C | G | 3 | a0001c0001t0001g0111a0001c0002t0001g0110a0001c0002t0001g0112 | 3 | HG01081.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194-13062C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276074 | ||||||
| chr8:91276236
|
TAAAA | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-12898_194-1289 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91276236 | |||||
| chr8:91276382
|
T | C | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-12754T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276382 | ||||||
| chr8:91276419
|
T | C | 1 | a0001c0002t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.194-12717T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276419 | ||||||
| chr8:91276452
|
C | T | 2 | a0001c0002t0015g0024a0001c0002t0022g0023 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194-12684C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276452 | ||||||
| chr8:91276505
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-12631G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276505 | ||||||
| chr8:91276516
|
C | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-12620C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276516 | ||||||
| chr8:91276650
|
T | C | 16 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(13): Show | 16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.194-12486T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276650 | ||||||
| chr8:91276794
|
G | C | 61 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(58): Show | 61 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.194-12342G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276794 | ||||||
| chr8:91276975
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.194-12161C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276975 | ||||||
| chr8:91277078
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.194-12058A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277078 | ||||||
| chr8:91277104
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02818.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-12032C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277104 | ||||||
| chr8:91277143
|
C | A | 6 | a0001c0001t0001g0010a0001c0001t0005g0108a0001c0001t0018g0124others(3): Show | 6 | HG02145.hp1 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-11993C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277143 | ||||||
| chr8:91277289
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-11847A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277289 | ||||||
| chr8:91277317
|
C | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.194-11819C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277317 | ||||||
| chr8:91277389
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-11747C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277389 | ||||||
| chr8:91277840
|
CAA | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-11295_194-1129 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277840 | ||||||
| chr8:91277903
|
C | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-11233C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277903 | ||||||
| chr8:91277904
|
CAT | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-11227_194-1122 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91277904 | |||||
| chr8:91277912
|
A | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-11224A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277912 | ||||||
| chr8:91278087
|
A | G | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-11049A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278087 | ||||||
| chr8:91278230
|
G | GA | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-10896dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91278230 | |||||
| chr8:91278230
|
GA | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-10896delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91278230 | |||||
| chr8:91278300
|
G | A | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-10836G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278300 | ||||||
| chr8:91278416
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(25): Show | 28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-10720G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278416 | ||||||
| chr8:91278540
|
T | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-10596T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278540 | ||||||
| chr8:91278613
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-10523A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278613 | ||||||
| chr8:91278726
|
C | T | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-10410C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278726 | ||||||
| chr8:91278794
|
A | G | 51 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-10342A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278794 | ||||||
| chr8:91278828
|
A | G | 61 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(58): Show | 61 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.194-10308A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278828 | ||||||
| chr8:91278837
|
G | A | 3 | a0001c0001t0004g0202a0001c0001t0012g0117a0001c0002t0004g0203 | 3 | HG02257.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.194-10299G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278837 | ||||||
| chr8:91279058
|
A | G | 1 | a0001c0001t0007g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.194-10078A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279058 | ||||||
| chr8:91279059
|
T | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-10077T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279059 | ||||||
| chr8:91279123
|
GTGTATAT others(5): Show |
G | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.194-10011_194-1000 others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279123 | |||||
| chr8:91279125
|
G | A | 8 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0139others(5): Show | 8 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-10011G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279125 | ||||||
| chr8:91279125
|
G | GTA | 13 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.194-9971_194-9970d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTATA | 25 | a0001c0001t0001g0043a0001c0001t0001g0128a0001c0001t0001g0151others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.194-9973_194-9970d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTATATA | 5 | a0001c0001t0001g0154a0001c0001t0001g0181a0001c0001t0001g0199others(2): Show | 5 | HG01123.hp1 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-9975_194-9970d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0182 | 3 | HG02300.hp2 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.194-9977_194-9970d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTATATAT others(3): Show |
5 | a0001c0001t0001g0153a0001c0001t0001g0160a0001c0001t0004g0188others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-9979_194-9970d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0009g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.194-9981_194-9970d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTGTATA | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTGTATAT others(5): Show |
1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194-10010_194-1000 others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTGTGTAT others(1): Show |
3 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0002t0002g0121 | 3 | HG02895.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTGTGTAT others(3): Show |
3 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0005t0006g0106 | 3 | HG06807.hp2 NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
G | GTGTGTGT others(3): Show |
3 | a0001c0001t0001g0119a0001c0001t0005g0004a0001c0002t0002g0047 | 3 | HG01109.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTA | G | 5 | a0001c0001t0001g0010a0001c0001t0002g0001a0001c0001t0002g0072others(2): Show | 6 | HG02004.hp2 HG02145.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-9971_194-9970d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATA | G | 16 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0050others(13): Show | 16 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-9973_194-9970d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATA | G | 16 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0056others(13): Show | 16 | HG00280.hp2 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-9975_194-9970d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(1): Show |
G | 40 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0037others(37): Show | 41 | HG00438.hp2 HG00609.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.194-9977_194-9970d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(3): Show |
G | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0089others(4): Show | 7 | HG01243.hp1 HG01978.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-9979_194-9970d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-9981_194-9970d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0002g0176a0001c0001t0004g0202 | 2 | HG02148.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.194-9983_194-9970d others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(15): Show |
G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.194-9991_194-9970d others(24): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(17): Show |
G | 1 | a0002c0003t0004g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.194-9993_194-9970d others(26): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279125
|
GTATATAT others(21): Show |
G | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-9997_194-9970d others(30): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | |||||
| chr8:91279127
|
A | G | 4 | a0001c0001t0018g0124a0001c0002t0001g0186a0001c0002t0002g0146others(1): Show | 4 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-10009A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279127 | ||||||
| chr8:91279129
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0018g0124a0001c0002t0001g0186others(2): Show | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-10007A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279129 | ||||||
| chr8:91279131
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0061others(6): Show | 9 | HG00741.hp2 HG01081.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-10005A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279131 | ||||||
| chr8:91279133
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.194-9986_194-9985i others(20): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279133 | |||||
| chr8:91279133
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0111a0001c0002t0001g0110others(3): Show | 6 | HG01081.hp2 HG01255.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-10003A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279133 | ||||||
| chr8:91279135
|
A | G | 2 | a0001c0001t0001g0010a0001c0008t0001g0031 | 2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.194-10001A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279135 | ||||||
| chr8:91279137
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.194-9982_194-9981i others(20): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279137 | |||||
| chr8:91279137
|
A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG01175.hp2 HG01515.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.194-9986_194-9985i others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279137 | |||||
| chr8:91279137
|
A | G | 5 | a0001c0001t0001g0010a0001c0002t0001g0045a0001c0002t0015g0024others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-9999A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279137 | ||||||
| chr8:91279139
|
A | G | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194-9997A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279139 | ||||||
| chr8:91279153
|
ATATATAT others(7): Show |
A | 4 | a0001c0001t0001g0101a0001c0002t0001g0103a0001c0002t0009g0102others(1): Show | 4 | HG00735.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-9979_194-9966d others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279153 | |||||
| chr8:91279155
|
A | G | 11 | a0001c0001t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.194-9981A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279155 | ||||||
| chr8:91279155
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0105a0001c0001t0023g0104 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.194-9977_194-9966d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279155 | |||||
| chr8:91279169
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-9967A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279169 | ||||||
| chr8:91279371
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-9765A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279371 | ||||||
| chr8:91279646
|
G | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-9490G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279646 | ||||||
| chr8:91279716
|
C | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0196others(3): Show | 7 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-9420C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279716 | ||||||
| chr8:91279721
|
G | A | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.194-9415G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279721 | ||||||
| chr8:91279736
|
T | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-9400T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279736 | ||||||
| chr8:91279795
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-9341G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279795 | ||||||
| chr8:91280033
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.194-9103G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280033 | ||||||
| chr8:91280386
|
C | T | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-8750C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280386 | ||||||
| chr8:91280523
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-8613C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280523 | ||||||
| chr8:91280567
|
C | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-8569C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280567 | ||||||
| chr8:91280641
|
A | G | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-8495A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280641 | ||||||
| chr8:91280710
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.194-8426T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280710 | ||||||
| chr8:91280784
|
C | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(2): Show | 5 | HG01978.hp1 HG02015.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-8352C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280784 | ||||||
| chr8:91280787
|
C | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-8349C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280787 | ||||||
| chr8:91281042
|
A | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0111others(35): Show | 38 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.194-8094A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281042 | ||||||
| chr8:91281124
|
C | A | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-8012C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281124 | ||||||
| chr8:91281192
|
A | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-7944A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281192 | ||||||
| chr8:91281302
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-7834G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281302 | ||||||
| chr8:91281481
|
C | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-7655C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281481 | ||||||
| chr8:91281482
|
T | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-7654T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281482 | ||||||
| chr8:91281521
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-7615G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281521 | ||||||
| chr8:91281522
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-7614G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281522 | ||||||
| chr8:91281811
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-7325C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281811 | ||||||
| chr8:91281814
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(79): Show | 85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-7322G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281814 | ||||||
| chr8:91281876
|
C | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(79): Show | 85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-7260C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281876 | ||||||
| chr8:91282060
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-7076A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282060 | ||||||
| chr8:91282150
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.194-6986G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282150 | ||||||
| chr8:91282437
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-6699A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282437 | ||||||
| chr8:91282557
|
A | T | 4 | a0001c0001t0001g0030a0001c0002t0015g0024a0001c0002t0022g0023others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-6579A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282557 | ||||||
| chr8:91282692
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-6444T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282692 | ||||||
| chr8:91282841
|
C | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-6295C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282841 | ||||||
| chr8:91282886
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-6250C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282886 | ||||||
| chr8:91282887
|
C | T | 3 | a0001c0002t0001g0187a0001c0002t0008g0189a0001c0002t0008g0190 | 3 | HG00733.hp2 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.194-6249C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282887 | ||||||
| chr8:91282924
|
TC | T | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-6211delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282924 | ||||||
| chr8:91283657
|
C | G | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.194-5479C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283657 | ||||||
| chr8:91283773
|
C | T | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.194-5363C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283773 | ||||||
| chr8:91283797
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-5339T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283797 | ||||||
| chr8:91283838
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-5298T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283838 | ||||||
| chr8:91283939
|
G | A | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-5197G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283939 | ||||||
| chr8:91283969
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-5167C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283969 | ||||||
| chr8:91284045
|
T | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.194-5091T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284045 | ||||||
| chr8:91284100
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-5036G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284100 | ||||||
| chr8:91284119
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(79): Show | 85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-5017G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284119 | ||||||
| chr8:91284215
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-4921A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284215 | ||||||
| chr8:91284230
|
A | G | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4906A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284230 | ||||||
| chr8:91284322
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-4814G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284322 | ||||||
| chr8:91284377
|
A | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-4759A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284377 | ||||||
| chr8:91284411
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(79): Show | 85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-4725A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284411 | ||||||
| chr8:91284483
|
A | C | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4653A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284483 | ||||||
| chr8:91284537
|
A | G | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4599A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284537 | ||||||
| chr8:91284651
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.194-4485A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284651 | ||||||
| chr8:91284664
|
T | C | 3 | a0001c0001t0005g0004a0001c0002t0002g0046a0001c0002t0002g0047 | 3 | HG01070.hp2 HG01109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.194-4472T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284664 | ||||||
| chr8:91284670
|
A | G | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-4466A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284670 | ||||||
| chr8:91284831
|
G | T | 2 | a0002c0003t0001g0135a0002c0003t0001g0136 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.194-4305G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284831 | ||||||
| chr8:91285031
|
A | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4105A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285031 | ||||||
| chr8:91285047
|
A | T | 1 | a0002c0003t0004g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.194-4089A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285047 | ||||||
| chr8:91285106
|
G | T | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-4030G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285106 | ||||||
| chr8:91285159
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-3977T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285159 | ||||||
| chr8:91285211
|
C | T | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.194-3925C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285211 | ||||||
| chr8:91285261
|
G | A | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-3875G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285261 | ||||||
| chr8:91285309
|
T | TTCA | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-3823_194-3821d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91285309 | |||||
| chr8:91285358
|
G | C | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.194-3778G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285358 | ||||||
| chr8:91285380
|
C | A | 1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194-3756C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285380 | ||||||
| chr8:91285433
|
G | A | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-3703G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285433 | ||||||
| chr8:91286036
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.194-3100A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286036 | ||||||
| chr8:91286197
|
G | A | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2939G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286197 | ||||||
| chr8:91286331
|
G | A | 3 | a0001c0002t0015g0024a0001c0002t0022g0023a0004c0011t0014g0022 | 3 | HG01891.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194-2805G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286331 | ||||||
| chr8:91286375
|
A | G | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-2761A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286375 | ||||||
| chr8:91286466
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(79): Show | 85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-2670T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286466 | ||||||
| chr8:91286515
|
G | A | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-2621G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286515 | ||||||
| chr8:91286723
|
G | A | 2 | a0001c0002t0002g0146a0001c0002t0002g0147 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.194-2413G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286723 | ||||||
| chr8:91286866
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.194-2270A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286866 | ||||||
| chr8:91287093
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0018g0124 | 4 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-2043T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287093 | ||||||
| chr8:91287633
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(140): Show | 146 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.194-1503T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287633 | ||||||
| chr8:91287879
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(66): Show | 71 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.194-1257C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287879 | ||||||
| chr8:91287939
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-1197C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287939 | ||||||
| chr8:91288156
|
T | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(119): Show | 125 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.194-980T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288156 | ||||||
| chr8:91288182
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.194-954C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288182 | ||||||
| chr8:91288285
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-851G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288285 | ||||||
| chr8:91288601
|
T | A | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.194-535T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288601 | ||||||
| chr8:91288618
|
C | CT | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(83): Show | 89 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.194-517dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91288618 | |||||
| chr8:91288743
|
C | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-393C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288743 | ||||||
| chr8:91288809
|
A | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(66): Show | 71 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.194-327A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288809 | ||||||
| chr8:91288927
|
A | T | 4 | a0001c0001t0001g0030a0001c0002t0015g0024a0001c0002t0022g0023others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-209A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288927 | ||||||
| chr8:91289021
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.194-115G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91289021 | ||||||
| chr8:91289727
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.304+481A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91289727 | ||||||
| chr8:91289928
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.304+682T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91289928 | ||||||
| chr8:91290306
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.304+1060C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290306 | ||||||
| chr8:91290570
|
T | C | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.304+1324T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290570 | ||||||
| chr8:91290590
|
G | A | 4 | a0001c0001t0001g0030a0001c0002t0015g0024a0001c0002t0022g0023others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+1344G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290590 | ||||||
| chr8:91290636
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.304+1390T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290636 | ||||||
| chr8:91290953
|
T | G | 32 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(29): Show | 32 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.304+1707T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290953 | ||||||
| chr8:91291055
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.304+1809G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291055 | ||||||
| chr8:91291131
|
A | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(140): Show | 146 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.304+1885A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291131 | ||||||
| chr8:91291205
|
A | G | 2 | a0001c0001t0001g0119a0001c0002t0002g0121 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.304+1959A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291205 | ||||||
| chr8:91291413
|
G | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304+2167G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291413 | ||||||
| chr8:91291735
|
C | T | 8 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.304+2489C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291735 | ||||||
| chr8:91291855
|
G | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.304+2609G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291855 | ||||||
| chr8:91291890
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(117): Show | 123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.304+2644A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291890 | ||||||
| chr8:91292001
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0196others(6): Show | 10 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.304+2755G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292001 | ||||||
| chr8:91292090
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.304+2844G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292090 | ||||||
| chr8:91292112
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.304+2866T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292112 | ||||||
| chr8:91292291
|
G | A | 1 | a0001c0001t0005g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.304+3045G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292291 | ||||||
| chr8:91292562
|
T | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(7): Show | 10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.305-2969T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292562 | ||||||
| chr8:91292732
|
G | GT | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-2789dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 91292732 | |||||
| chr8:91292742
|
T | A | 3 | a0001c0002t0015g0024a0001c0002t0022g0023a0004c0011t0014g0022 | 3 | HG01891.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.305-2789T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292742 | ||||||
| chr8:91292743
|
A | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0154a0001c0001t0018g0124 | 3 | HG01123.hp1 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.305-2788A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292743 | ||||||
| chr8:91292866
|
A | G | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-2665A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292866 | ||||||
| chr8:91293035
|
A | G | 22 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.305-2496A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293035 | ||||||
| chr8:91293050
|
T | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | NA19010.hp2 NA19063.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.305-2481T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293050 | ||||||
| chr8:91293328
|
C | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-2203C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293328 | ||||||
| chr8:91293689
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-1842C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293689 | ||||||
| chr8:91293798
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-1733T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293798 | ||||||
| chr8:91293885
|
C | T | 1 | a0001c0001t0007g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.305-1646C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293885 | ||||||
| chr8:91294012
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.305-1519A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294012 | ||||||
| chr8:91294161
|
C | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0134 | 3 | HG02572.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.305-1370C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294161 | ||||||
| chr8:91294191
|
T | C | 22 | a0001c0001t0001g0030a0001c0001t0001g0111a0001c0001t0001g0119others(19): Show | 22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.305-1340T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294191 | ||||||
| chr8:91294429
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-1102A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294429 | ||||||
| chr8:91294510
|
G | A | 3 | a0001c0001t0001g0111a0001c0002t0001g0110a0001c0002t0001g0112 | 3 | HG01081.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.305-1021G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294510 | ||||||
| chr8:91294654
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.305-877G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294654 | ||||||
| chr8:91294743
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.305-788A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294743 | ||||||
| chr8:91295006
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.305-525T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295006 | ||||||
| chr8:91295239
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.305-292C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295239 | ||||||
| chr8:91295357
|
C | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.305-174C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295357 | ||||||
| chr8:91295373
|
A | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-158A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295373 | ||||||
| chr8:91295386
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.305-145G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295386 | ||||||
| chr8:91295750
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(94): Show | 100 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.477+47C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91295750 | ||||||
| chr8:91295900
|
A | G | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.477+197A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91295900 | ||||||
| chr8:91296028
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0145others(4): Show | 7 | HG00609.hp1 HG02132.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+325C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296028 | ||||||
| chr8:91296029
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.477+326G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296029 | ||||||
| chr8:91296429
|
G | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.477+726G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296429 | ||||||
| chr8:91296509
|
G | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+806G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296509 | ||||||
| chr8:91296629
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.477+926G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296629 | ||||||
| chr8:91297204
|
G | A | 1 | a0001c0004t0002g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.477+1501G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297204 | ||||||
| chr8:91297260
|
C | T | 1 | a0001c0002t0003g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.477+1557C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297260 | ||||||
| chr8:91297540
|
A | G | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.477+1837A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297540 | ||||||
| chr8:91297550
|
A | T | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.477+1847A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297550 | ||||||
| chr8:91298116
|
C | T | 2 | a0001c0001t0001g0018a0002c0003t0019g0009 | 2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.477+2413C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91298116 | ||||||
| chr8:91298266
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 7 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+2563T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91298266 | ||||||
| chr8:91298471
|
T | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.477+2768T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91298471 | ||||||
| chr8:91299016
|
C | A | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.477+3313C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299016 | ||||||
| chr8:91299180
|
T | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+3477T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299180 | ||||||
| chr8:91299184
|
A | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.477+3481A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299184 | ||||||
| chr8:91299417
|
T | TTTAAG | 69 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(66): Show | 69 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.477+3717_477+3718i others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91299417 | |||||
| chr8:91299528
|
T | C | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 8 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3825T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299528 | ||||||
| chr8:91299565
|
T | TA | 4 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+3863dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91299565 | |||||
| chr8:91299670
|
A | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.477+3967A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299670 | ||||||
| chr8:91299981
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.477+4278T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299981 | ||||||
| chr8:91300400
|
AT | A | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 8 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+4712delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91300400 | |||||
| chr8:91300437
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0162 | 2 | HG00438.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.477+4734A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300437 | ||||||
| chr8:91300447
|
G | T | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.477+4744G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300447 | ||||||
| chr8:91300455
|
G | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0162 | 2 | HG00438.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.477+4752G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300455 | ||||||
| chr8:91300460
|
C | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0162 | 2 | HG00438.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.477+4757C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300460 | ||||||
| chr8:91300466
|
C | T | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0002c0003t0004g0095others(3): Show | 6 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+4763C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300466 | ||||||
| chr8:91300662
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.477+4959G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300662 | ||||||
| chr8:91300928
|
A | AT | 64 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(61): Show | 65 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.477+5229dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91300928 | |||||
| chr8:91301154
|
G | A | 16 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(13): Show | 16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.477+5451G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301154 | ||||||
| chr8:91301800
|
TTA | T | 7 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(4): Show | 7 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+6099_477+6100d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91301800 | |||||
| chr8:91301801
|
TA | T | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+6099delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301801 | ||||||
| chr8:91301888
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.477+6185A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301888 | ||||||
| chr8:91301970
|
T | C | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.477+6267T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301970 | ||||||
| chr8:91302409
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+6706C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302409 | ||||||
| chr8:91302542
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.477+6839G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302542 | ||||||
| chr8:91302818
|
C | CTTTTTT | 20 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(17): Show | 20 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.477+7126_477+7131d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91302818 | |||||
| chr8:91302818
|
CT | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0030others(98): Show | 103 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.477+7131delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91302818 | |||||
| chr8:91302827
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.477+7124T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302827 | ||||||
| chr8:91302917
|
C | G | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.477+7214C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302917 | ||||||
| chr8:91302948
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.477+7245G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302948 | ||||||
| chr8:91303024
|
G | A | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.477+7321G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303024 | ||||||
| chr8:91303219
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+7516A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303219 | ||||||
| chr8:91303369
|
C | T | 2 | a0001c0002t0015g0024a0001c0002t0022g0023 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.477+7666C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303369 | ||||||
| chr8:91303393
|
A | G | 13 | a0001c0001t0001g0119a0001c0001t0005g0004a0001c0001t0007g0005others(10): Show | 13 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.477+7690A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303393 | ||||||
| chr8:91303701
|
G | T | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+7998G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303701 | ||||||
| chr8:91303869
|
CAGG | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.477+8174_477+8176d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91303869 | |||||
| chr8:91303971
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+8268T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303971 | ||||||
| chr8:91304114
|
C | T | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.477+8411C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91304114 | ||||||
| chr8:91304403
|
A | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(46): Show | 50 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.477+8700A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91304403 | ||||||
| chr8:91304817
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG01175.hp1 HG01192.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+9114T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91304817 | ||||||
| chr8:91305031
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.477+9328T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305031 | ||||||
| chr8:91305142
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.477+9439C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305142 | ||||||
| chr8:91305241
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.477+9538T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305241 | ||||||
| chr8:91305457
|
C | A | 1 | a0001c0001t0005g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.477+9754C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305457 | ||||||
| chr8:91305581
|
C | G | 16 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(13): Show | 16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.477+9878C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305581 | ||||||
| chr8:91305614
|
A | AGCATCAG others(2): Show |
5 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(2): Show | 5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+9914_477+9922d others(11): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91305614 | |||||
| chr8:91305742
|
TTAGA | T | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+10044_477+1004 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91305742 | |||||
| chr8:91306281
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+10578A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306281 | ||||||
| chr8:91306294
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.477+10591G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306294 | ||||||
| chr8:91306357
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.477+10654C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306357 | ||||||
| chr8:91306370
|
GC | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0184 | 2 | HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.477+10668delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306370 | ||||||
| chr8:91306484
|
A | G | 7 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+10781A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306484 | ||||||
| chr8:91306523
|
A | G | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.477+10820A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306523 | ||||||
| chr8:91306569
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.477+10866A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306569 | ||||||
| chr8:91306665
|
T | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(49): Show | 53 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.477+10962T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306665 | ||||||
| chr8:91306714
|
AT | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.477+11024delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91306714 | |||||
| chr8:91306788
|
TAACCTGG others(3): Show |
T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.477+11086_477+1109 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306788 | ||||||
| chr8:91306923
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.477+11220A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306923 | ||||||
| chr8:91306969
|
C | G | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.478-11247C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306969 | ||||||
| chr8:91307126
|
G | A | 1 | a0001c0002t0003g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.478-11090G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307126 | ||||||
| chr8:91307332
|
A | G | 4 | a0001c0001t0001g0013a0001c0002t0003g0017a0001c0002t0003g0020others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-10884A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307332 | ||||||
| chr8:91307409
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.478-10807A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307409 | ||||||
| chr8:91307444
|
A | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0090 | 2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.478-10772A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307444 | ||||||
| chr8:91307458
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.478-10758A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307458 | ||||||
| chr8:91307477
|
T | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-10739T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307477 | ||||||
| chr8:91307591
|
T | C | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-10625T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307591 | ||||||
| chr8:91307660
|
G | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-10556G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307660 | ||||||
| chr8:91307722
|
C | T | 5 | a0001c0001t0001g0137a0001c0002t0001g0014a0001c0002t0001g0015others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-10494C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307722 | ||||||
| chr8:91307746
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(127): Show | 133 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.478-10470A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307746 | ||||||
| chr8:91307816
|
T | TA | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(161): Show | 167 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.478-10392dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91307816 | |||||
| chr8:91307833
|
TTAAAA | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-10366_478-1036 others(9): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91307833 | |||||
| chr8:91307872
|
A | AT | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-10337dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91307872 | |||||
| chr8:91307891
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0119others(16): Show | 20 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-10325G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307891 | ||||||
| chr8:91307899
|
A | G | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.478-10317A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307899 | ||||||
| chr8:91308246
|
G | GGT | 23 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0058others(20): Show | 24 | HG01175.hp2 HG01261.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.478-9937_478-9936d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | |||||
| chr8:91308246
|
G | GGTGT | 11 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0122others(8): Show | 12 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478-9939_478-9936d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | |||||
| chr8:91308246
|
GGT | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0079others(7): Show | 10 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-9937_478-9936d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | |||||
| chr8:91308246
|
GGTGT | G | 11 | a0001c0001t0001g0081a0001c0001t0001g0111a0001c0001t0002g0063others(8): Show | 11 | HG00558.hp2 HG01070.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-9939_478-9936d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | |||||
| chr8:91308393
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.478-9823G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308393 | ||||||
| chr8:91308412
|
C | CT | 57 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(54): Show | 58 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.478-9801dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308412 | |||||
| chr8:91308518
|
T | C | 1 | a0001c0002t0002g0148 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.478-9698T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308518 | ||||||
| chr8:91308562
|
A | C | 2 | a0001c0001t0001g0173a0001c0001t0002g0063 | 2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.478-9654A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308562 | ||||||
| chr8:91308564
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-9652A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308564 | ||||||
| chr8:91308569
|
A | G | 2 | a0001c0001t0004g0202a0001c0001t0012g0117 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.478-9647A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308569 | ||||||
| chr8:91308688
|
C | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-9528C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308688 | ||||||
| chr8:91309012
|
T | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-9204T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309012 | ||||||
| chr8:91309247
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.478-8969T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309247 | ||||||
| chr8:91309506
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.478-8710A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309506 | ||||||
| chr8:91309885
|
G | A | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478-8331G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309885 | ||||||
| chr8:91309897
|
A | G | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0002c0003t0004g0095others(3): Show | 6 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-8319A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309897 | ||||||
| chr8:91309915
|
T | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-8301T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309915 | ||||||
| chr8:91310145
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.478-8071C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310145 | ||||||
| chr8:91310259
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.478-7957A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310259 | ||||||
| chr8:91310549
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.478-7667G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310549 | ||||||
| chr8:91310683
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0096 | 2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.478-7533G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310683 | ||||||
| chr8:91310816
|
G | T | 11 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-7400G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310816 | ||||||
| chr8:91310851
|
C | CA | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(55): Show | 59 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.478-7362dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91310851 | |||||
| chr8:91310991
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.478-7225C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310991 | ||||||
| chr8:91311115
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.478-7101A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311115 | ||||||
| chr8:91311229
|
G | T | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.478-6987G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311229 | ||||||
| chr8:91311275
|
A | G | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478-6941A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311275 | ||||||
| chr8:91311391
|
G | A | 2 | a0001c0002t0002g0146a0001c0002t0002g0147 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.478-6825G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311391 | ||||||
| chr8:91311431
|
TTATATA | T | 2 | a0001c0001t0001g0205a0001c0001t0021g0206 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.478-6778_478-6773d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91311431 | |||||
| chr8:91311448
|
C | T | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.478-6768C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311448 | ||||||
| chr8:91311596
|
C | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0033others(65): Show | 70 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.478-6620C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311596 | ||||||
| chr8:91311722
|
G | A | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-6494G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311722 | ||||||
| chr8:91312056
|
C | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-6160C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312056 | ||||||
| chr8:91312262
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.478-5954C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312262 | ||||||
| chr8:91312273
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478-5943A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312273 | ||||||
| chr8:91312370
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.478-5846T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312370 | ||||||
| chr8:91312379
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.478-5837A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312379 | ||||||
| chr8:91312380
|
T | C | 3 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0120 | 3 | HG00558.hp2 NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.478-5836T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312380 | ||||||
| chr8:91312560
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.478-5656T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312560 | ||||||
| chr8:91312641
|
C | CTG | 2 | a0001c0001t0001g0105a0001c0001t0023g0104 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.478-5543_478-5542d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312641
|
C | CTGTG | 5 | a0001c0001t0001g0101a0001c0001t0005g0099a0001c0002t0001g0103others(2): Show | 5 | HG00735.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-5545_478-5542d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312641
|
CTG | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(48): Show | 52 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.478-5543_478-5542d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312641
|
CTGTG | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0018others(76): Show | 80 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.478-5545_478-5542d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312641
|
CTGTGTG | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0025others(56): Show | 60 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.478-5547_478-5542d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312641
|
CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0002t0003g0204 | 3 | HG00639.hp2 HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.478-5549_478-5542d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312641
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0002t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.478-5551_478-5542d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | |||||
| chr8:91312713
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0193 | 2 | HG03017.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.478-5503C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312713 | ||||||
| chr8:91312864
|
A | T | 17 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-5352A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312864 | ||||||
| chr8:91312917
|
A | T | 2 | a0001c0002t0001g0197a0001c0002t0002g0029 | 2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.478-5299A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312917 | ||||||
| chr8:91312966
|
C | G | 5 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(2): Show | 5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-5250C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312966 | ||||||
| chr8:91313043
|
A | G | 4 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0001g0191others(1): Show | 4 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-5173A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313043 | ||||||
| chr8:91313515
|
A | G | 19 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(16): Show | 19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.478-4701A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313515 | ||||||
| chr8:91313685
|
A | G | 73 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0032others(70): Show | 75 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.478-4531A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313685 | ||||||
| chr8:91313696
|
C | T | 2 | a0001c0001t0001g0002a0004c0011t0014g0022 | 3 | HG01891.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.478-4520C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313696 | ||||||
| chr8:91313873
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.478-4343C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313873 | ||||||
| chr8:91314389
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-3827A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314389 | ||||||
| chr8:91314461
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.478-3755G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314461 | ||||||
| chr8:91314635
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.478-3581T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314635 | ||||||
| chr8:91314736
|
C | T | 17 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-3480C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314736 | ||||||
| chr8:91314765
|
T | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(16): Show | 19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.478-3451T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314765 | ||||||
| chr8:91314859
|
G | C | 5 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(2): Show | 5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-3357G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314859 | ||||||
| chr8:91314931
|
T | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-3285T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314931 | ||||||
| chr8:91315164
|
C | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-3052C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315164 | ||||||
| chr8:91315200
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.478-3016T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315200 | ||||||
| chr8:91315291
|
A | C | 17 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-2925A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315291 | ||||||
| chr8:91315326
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0096 | 2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.478-2890G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315326 | ||||||
| chr8:91315456
|
C | CA | 32 | a0001c0001t0001g0030a0001c0001t0001g0048a0001c0001t0001g0052others(29): Show | 32 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.478-2745dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91315456 | |||||
| chr8:91315471
|
A | AAT | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-2745_478-2744i others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315471 | ||||||
| chr8:91315471
|
A | AT | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-2745_478-2744i others(3): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315471 | ||||||
| chr8:91315591
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-2625C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315591 | ||||||
| chr8:91315598
|
T | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-2618T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315598 | ||||||
| chr8:91315758
|
C | G | 1 | a0001c0007t0002g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.478-2458C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315758 | ||||||
| chr8:91315790
|
T | A | 1 | a0001c0002t0002g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.478-2426T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315790 | ||||||
| chr8:91316046
|
G | A | 6 | a0001c0001t0001g0200a0001c0001t0001g0205a0001c0001t0009g0201others(3): Show | 6 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-2170G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316046 | ||||||
| chr8:91316058
|
C | T | 17 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-2158C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316058 | ||||||
| chr8:91316222
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.478-1994C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316222 | ||||||
| chr8:91316223
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02615.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.478-1993G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316223 | ||||||
| chr8:91316370
|
C | T | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478-1846C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316370 | ||||||
| chr8:91316451
|
A | AT | 7 | a0001c0001t0001g0028a0001c0001t0001g0141a0001c0001t0001g0169others(4): Show | 7 | HG01069.hp1 HG01256.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1726dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
A | ATT | 11 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0097others(8): Show | 11 | HG00642.hp2 HG00733.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-1727_478-1726d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
AT | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0128others(9): Show | 13 | HG01175.hp1 HG01175.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-1726delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATT | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0129others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.478-1727_478-1726d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTT | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 26 | HG00609.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.478-1728_478-1726d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTT | A | 10 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0049others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-1729_478-1726d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTT | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0035others(38): Show | 43 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.478-1730_478-1726d others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTT | A | 33 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0039others(30): Show | 33 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.478-1731_478-1726d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0003g0113others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-1737_478-1726d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.478-1738_478-1726d others(15): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTTT others(9): Show |
A | 4 | a0001c0001t0001g0171a0001c0001t0001g0199a0001c0002t0001g0112others(1): Show | 4 | HG01433.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1741_478-1726d others(18): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTTT others(10): Show |
A | 14 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0005g0004others(11): Show | 14 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-1742_478-1726d others(19): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.478-1743_478-1726d others(20): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316451
|
ATTTTTTT others(12): Show |
A | 2 | a0001c0002t0001g0045a0001c0008t0001g0031 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.478-1744_478-1726d others(21): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | |||||
| chr8:91316471
|
T | C | 1 | a0001c0008t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.478-1745T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316471 | ||||||
| chr8:91316725
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.478-1491A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316725 | ||||||
| chr8:91316806
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0173a0001c0001t0002g0063 | 3 | HG01993.hp2 HG02300.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.478-1410G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316806 | ||||||
| chr8:91316965
|
G | A | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 8 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1251G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316965 | ||||||
| chr8:91316988
|
T | TA | 15 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0084others(12): Show | 15 | HG01109.hp1 HG01891.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.478-1195dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
T | TAAAAAAA | 6 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0137others(3): Show | 6 | HG01069.hp1 HG01081.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1201_478-1195d others(9): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
T | TAAAAAAA others(1): Show |
9 | a0001c0001t0001g0026a0001c0001t0001g0073a0001c0001t0001g0096others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-1202_478-1195d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0097a0001c0002t0001g0187 | 2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.478-1204_478-1195d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
T | TAAAAAAA others(4): Show |
1 | a0001c0002t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.478-1205_478-1195d others(13): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
TA | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0033others(85): Show | 90 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.478-1195delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
TAA | T | 18 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0111others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.478-1196_478-1195d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91316988
|
TAAAAAAA others(12): Show |
T | 7 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-1213_478-1195d others(21): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | |||||
| chr8:91317178
|
A | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-1038A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317178 | ||||||
| chr8:91317360
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-856C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317360 | ||||||
| chr8:91317426
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.478-790T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317426 | ||||||
| chr8:91317939
|
GAT | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(124): Show | 128 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.478-259_478-258del others(2): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91317939 | |||||
| chr8:91317939
|
GATAT | G | 2 | a0001c0001t0001g0097a0001c0002t0003g0204 | 2 | HG00642.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.478-261_478-258del others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91317939 | |||||
| chr8:91317944
|
A | C | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.478-272A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317944 | ||||||
| chr8:91317956
|
A | AAAAT | 4 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0002g0001others(1): Show | 5 | HG02622.hp2 HG03195.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-260_478-259ins others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317956 | ||||||
| chr8:91317957
|
T | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0002g0001others(1): Show | 5 | HG02622.hp2 HG03195.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-259T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317957 | ||||||
| chr8:91317987
|
T | A | 2 | a0001c0001t0001g0142a0001c0001t0002g0138 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.478-229T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317987 | ||||||
| chr8:91317993
|
A | T | 3 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0055 | 3 | HG01256.hp1 HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.478-223A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317993 | ||||||
| chr8:91318005
|
A | AG | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-211_478-210ins others(1): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91318005 | ||||||
| chr8:91318189
|
C | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-27C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91318189 | ||||||
| chr8:91318473
|
A | G | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642+93A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91318473 | ||||||
| chr8:91318839
|
A | G | 48 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(45): Show | 48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+459A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91318839 | ||||||
| chr8:91318980
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(45): Show | 48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+600C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91318980 | ||||||
| chr8:91319073
|
G | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.642+693G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319073 | ||||||
| chr8:91319174
|
T | G | 48 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(45): Show | 48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+794T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319174 | ||||||
| chr8:91319223
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642+843T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319223 | ||||||
| chr8:91319662
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+1282T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319662 | ||||||
| chr8:91319805
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.642+1425A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319805 | ||||||
| chr8:91319965
|
A | AG | 48 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(45): Show | 48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+1587dupG | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91319965 | |||||
| chr8:91320049
|
T | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.642+1669T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91320049 | ||||||
| chr8:91320537
|
C | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+2157C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91320537 | ||||||
| chr8:91321193
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.642+2813T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321193 | ||||||
| chr8:91321227
|
A | G | 2 | a0001c0001t0001g0003a0001c0002t0001g0198 | 3 | HG00738.hp2 HG01192.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.642+2847A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321227 | ||||||
| chr8:91321245
|
G | A | 1 | a0001c0002t0008g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.642+2865G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321245 | ||||||
| chr8:91321418
|
G | C | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+3038G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321418 | ||||||
| chr8:91321908
|
CT | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0032others(71): Show | 76 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.642+3529delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321908 | ||||||
| chr8:91322158
|
C | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(45): Show | 48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+3778C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322158 | ||||||
| chr8:91322205
|
C | CTTCT | 2 | a0001c0001t0001g0002a0001c0002t0003g0204 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.642+3826_642+3829d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91322205 | |||||
| chr8:91322417
|
G | A | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+4037G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322417 | ||||||
| chr8:91322429
|
T | G | 2 | a0002c0003t0001g0135a0002c0003t0001g0136 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.642+4049T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322429 | ||||||
| chr8:91322823
|
G | T | 1 | a0001c0001t0004g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642+4443G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322823 | ||||||
| chr8:91322824
|
C | T | 1 | a0001c0001t0004g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642+4444C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322824 | ||||||
| chr8:91322948
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+4568A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322948 | ||||||
| chr8:91323174
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(55): Show | 59 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.642+4794T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323174 | ||||||
| chr8:91323411
|
A | G | 19 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(16): Show | 19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+5031A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323411 | ||||||
| chr8:91323444
|
C | A | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+5064C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323444 | ||||||
| chr8:91323461
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(5): Show | 8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+5081A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323461 | ||||||
| chr8:91323627
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.642+5247C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323627 | ||||||
| chr8:91323818
|
C | CT | 12 | a0001c0001t0001g0030a0001c0001t0001g0101a0001c0001t0001g0105others(9): Show | 12 | HG00735.hp1 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.642+5456dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | |||||
| chr8:91323818
|
C | CTT | 26 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(23): Show | 26 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.642+5455_642+5456d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | |||||
| chr8:91323818
|
CT | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0033others(68): Show | 73 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.642+5456delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | |||||
| chr8:91323818
|
CTT | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+5455_642+5456d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | |||||
| chr8:91323818
|
CTTTTTTT others(1): Show |
C | 19 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(16): Show | 19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+5449_642+5456d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | |||||
| chr8:91323843
|
T | C | 5 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(2): Show | 5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+5463T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323843 | ||||||
| chr8:91324058
|
G | A | 57 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(54): Show | 57 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.642+5678G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91324058 | ||||||
| chr8:91324271
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.642+5891T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91324271 | ||||||
| chr8:91324435
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.642+6055G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91324435 | ||||||
| chr8:91325235
|
G | A | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.642+6855G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325235 | ||||||
| chr8:91325283
|
T | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02155.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.642+6903T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325283 | ||||||
| chr8:91325416
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.642+7036C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325416 | ||||||
| chr8:91325483
|
G | A | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.642+7103G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325483 | ||||||
| chr8:91325647
|
C | A | 18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(15): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+7267C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325647 | ||||||
| chr8:91325694
|
C | T | 1 | a0001c0001t0021g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.642+7314C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325694 | ||||||
| chr8:91326164
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.642+7784T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326164 | ||||||
| chr8:91326284
|
A | G | 4 | a0001c0001t0001g0013a0001c0002t0003g0017a0001c0002t0003g0020others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+7904A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326284 | ||||||
| chr8:91326422
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-7873T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326422 | ||||||
| chr8:91326856
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.643-7439C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326856 | ||||||
| chr8:91326895
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.643-7400C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326895 | ||||||
| chr8:91326908
|
C | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0085others(12): Show | 16 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-7387C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326908 | ||||||
| chr8:91327022
|
G | A | 56 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(53): Show | 56 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.643-7273G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327022 | ||||||
| chr8:91327045
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.643-7250C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327045 | ||||||
| chr8:91327046
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.643-7249T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327046 | ||||||
| chr8:91327136
|
G | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-7159G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327136 | ||||||
| chr8:91327162
|
C | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(42): Show | 45 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.643-7133C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327162 | ||||||
| chr8:91327173
|
A | T | 4 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(1): Show | 4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-7122A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327173 | ||||||
| chr8:91327321
|
C | T | 1 | a0001c0008t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.643-6974C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327321 | ||||||
| chr8:91327419
|
A | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-6876A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327419 | ||||||
| chr8:91327550
|
A | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-6745A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327550 | ||||||
| chr8:91327627
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.643-6668G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327627 | ||||||
| chr8:91327907
|
G | A | 57 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(54): Show | 57 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.643-6388G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327907 | ||||||
| chr8:91328021
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.643-6274A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91328021 | ||||||
| chr8:91328116
|
T | A | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.643-6179T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91328116 | ||||||
| chr8:91328762
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0196others(3): Show | 7 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-5533G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91328762 | ||||||
| chr8:91329145
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0098 | 2 | HG00558.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.643-5150G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329145 | ||||||
| chr8:91329234
|
A | ATGTGTG | 47 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(44): Show | 47 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.643-5056_643-5051d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91329234 | |||||
| chr8:91329298
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.643-4997C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329298 | ||||||
| chr8:91329419
|
G | A | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.643-4876G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329419 | ||||||
| chr8:91329449
|
C | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.643-4846C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329449 | ||||||
| chr8:91329484
|
T | C | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-4811T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329484 | ||||||
| chr8:91329741
|
C | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-4554C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329741 | ||||||
| chr8:91329840
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0105others(6): Show | 10 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-4455T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329840 | ||||||
| chr8:91329874
|
T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.643-4421T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329874 | ||||||
| chr8:91330037
|
G | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(58): Show | 62 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.643-4258G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330037 | ||||||
| chr8:91330055
|
A | G | 47 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0025others(44): Show | 47 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.643-4240A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330055 | ||||||
| chr8:91330081
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.643-4214G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330081 | ||||||
| chr8:91330165
|
T | C | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.643-4130T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330165 | ||||||
| chr8:91330290
|
G | A | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.643-4005G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330290 | ||||||
| chr8:91330397
|
A | G | 6 | a0001c0001t0001g0200a0001c0001t0001g0205a0001c0001t0009g0201others(3): Show | 6 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-3898A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330397 | ||||||
| chr8:91330494
|
A | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-3801A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330494 | ||||||
| chr8:91330498
|
T | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-3797T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330498 | ||||||
| chr8:91330501
|
T | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.643-3794T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330501 | ||||||
| chr8:91330713
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0086 | 2 | HG00741.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.643-3582C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330713 | ||||||
| chr8:91330716
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0101a0001c0001t0001g0105others(7): Show | 10 | HG00735.hp1 HG01261.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-3579A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330716 | ||||||
| chr8:91331808
|
A | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-2487A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91331808 | ||||||
| chr8:91331910
|
A | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0081others(3): Show | 6 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-2385A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91331910 | ||||||
| chr8:91332103
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.643-2192G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332103 | ||||||
| chr8:91332144
|
C | CAT | 14 | a0001c0001t0001g0030a0001c0001t0001g0101a0001c0001t0001g0114others(11): Show | 14 | HG00735.hp1 HG01243.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-2137_643-2136d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332144 | |||||
| chr8:91332227
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0018g0124 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.643-2068A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332227 | ||||||
| chr8:91332250
|
A | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.643-2045A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332250 | ||||||
| chr8:91332351
|
A | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0105others(5): Show | 9 | HG00735.hp1 HG02486.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-1944A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332351 | ||||||
| chr8:91332370
|
A | G | 5 | a0001c0001t0005g0108a0001c0002t0001g0107a0001c0005t0006g0106others(2): Show | 5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1925A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332370 | ||||||
| chr8:91332395
|
T | TTATATTT others(27): Show |
18 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0199others(15): Show | 18 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-1887_643-1854d others(36): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332395 | |||||
| chr8:91332491
|
T | TAC | 32 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0050others(29): Show | 33 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.643-1762_643-1761d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
T | TACAC | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0040others(45): Show | 48 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.643-1764_643-1761d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
T | TACACAC | 12 | a0001c0001t0001g0043a0001c0001t0001g0126a0001c0001t0001g0128others(9): Show | 12 | HG00609.hp1 HG00741.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.643-1766_643-1761d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0002t0002g0121others(3): Show | 6 | HG02630.hp2 HG02895.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-1768_643-1761d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
T | TACACACA others(3): Show |
5 | a0001c0001t0001g0134a0001c0001t0005g0108a0001c0002t0001g0107others(2): Show | 5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1770_643-1761d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
TAC | T | 22 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0056others(19): Show | 22 | HG00609.hp2 HG00642.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.643-1762_643-1761d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
TACAC | T | 7 | a0001c0001t0001g0038a0001c0001t0001g0091a0001c0001t0001g0139others(4): Show | 7 | HG00280.hp2 HG00733.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1764_643-1761d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
TACACAC | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0127 | 3 | HG00438.hp2 HG01261.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.643-1766_643-1761d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.643-1770_643-1761d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332491
|
TACACACA others(5): Show |
T | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1772_643-1761d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | |||||
| chr8:91332697
|
A | AT | 7 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0005g0099others(4): Show | 7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1592dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332697 | |||||
| chr8:91332769
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.643-1526C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332769 | ||||||
| chr8:91332770
|
G | C | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-1525G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332770 | ||||||
| chr8:91332776
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1519T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332776 | ||||||
| chr8:91332965
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0127 | 2 | HG01261.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.643-1330C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332965 | ||||||
| chr8:91333373
|
A | G | 113 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0032others(110): Show | 114 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.643-922A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333373 | ||||||
| chr8:91333519
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(157): Show | 163 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.643-776A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333519 | ||||||
| chr8:91333537
|
C | T | 1 | a0001c0012t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.643-758C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333537 | ||||||
| chr8:91333616
|
TC | T | 2 | a0001c0001t0001g0105a0001c0001t0023g0104 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.643-678delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333616 | ||||||
| chr8:91333772
|
A | G | 1 | a0001c0002t0008g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.643-523A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333772 | ||||||
| chr8:91333959
|
G | T | 1 | a0001c0002t0002g0046 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.643-336G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333959 | ||||||
| chr8:91334234
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.643-61T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91334234 | ||||||
| chr8:91334620
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.795+173A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334620 | ||||||
| chr8:91334671
|
T | C | 1 | a0001c0002t0012g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.795+224T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334671 | ||||||
| chr8:91334710
|
T | C | 3 | a0001c0001t0001g0199a0001c0002t0001g0110a0001c0002t0001g0112 | 3 | HG02486.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.795+263T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334710 | ||||||
| chr8:91334993
|
A | C | 13 | a0001c0001t0001g0199a0001c0002t0001g0045a0001c0002t0001g0110others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.795+546A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334993 | ||||||
| chr8:91335213
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.795+766T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335213 | ||||||
| chr8:91335305
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(125): Show | 131 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.795+858C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335305 | ||||||
| chr8:91335354
|
T | C | 2 | a0001c0002t0008g0189a0001c0002t0008g0190 | 2 | HG00733.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.795+907T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335354 | ||||||
| chr8:91335385
|
A | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0055 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.795+938A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335385 | ||||||
| chr8:91335704
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.795+1257A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335704 | ||||||
| chr8:91335798
|
A | G | 22 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(19): Show | 22 | HG00733.hp2 HG01074.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.795+1351A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335798 | ||||||
| chr8:91335843
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.795+1396T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335843 | ||||||
| chr8:91335903
|
T | G | 4 | a0002c0003t0004g0095a0002c0003t0004g0156a0002c0003t0004g0157others(1): Show | 4 | HG00642.hp1 NA20752.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+1456T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335903 | ||||||
| chr8:91336004
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(29): Show | 34 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.795+1557C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336004 | ||||||
| chr8:91336023
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.795+1576C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336023 | ||||||
| chr8:91336064
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.795+1617A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336064 | ||||||
| chr8:91336338
|
G | A | 6 | a0001c0001t0005g0099a0001c0002t0001g0103a0001c0002t0009g0102others(3): Show | 6 | HG00735.hp1 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-1812G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336338 | ||||||
| chr8:91336401
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0001g0137others(4): Show | 7 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1749C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336401 | ||||||
| chr8:91336419
|
T | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(140): Show | 146 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.796-1731T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336419 | ||||||
| chr8:91336454
|
G | C | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.796-1696G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336454 | ||||||
| chr8:91336558
|
A | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0013others(69): Show | 73 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.796-1592A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336558 | ||||||
| chr8:91336607
|
A | C | 22 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(19): Show | 22 | HG00733.hp2 HG01074.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.796-1543A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336607 | ||||||
| chr8:91336670
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0119 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.796-1480G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336670 | ||||||
| chr8:91336745
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(29): Show | 34 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.796-1405G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336745 | ||||||
| chr8:91337145
|
CT | C | 19 | a0001c0001t0001g0199a0001c0001t0005g0099a0001c0002t0001g0045others(16): Show | 19 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.796-1004delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91337145 | ||||||
| chr8:91337661
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(126): Show | 132 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.796-489T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91337661 | ||||||
| chr8:91337955
|
CT | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(126): Show | 132 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.796-193delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 91337955 | |||||
| chr8:91338339
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.878+107T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338339 | ||||||
| chr8:91338456
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(51): Show | 56 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.878+224G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338456 | ||||||
| chr8:91338700
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.878+468C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338700 | ||||||
| chr8:91338741
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0023g0104 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.878+509G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338741 | ||||||
| chr8:91338769
|
A | G | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.878+537A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338769 | ||||||
| chr8:91338962
|
A | G | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.878+730A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338962 | ||||||
| chr8:91338976
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0013others(68): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.878+744G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338976 | ||||||
| chr8:91339137
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.878+905T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339137 | ||||||
| chr8:91339264
|
C | T | 1 | a0001c0001t0021g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.878+1032C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339264 | ||||||
| chr8:91339355
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.879-1049C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339355 | ||||||
| chr8:91339407
|
G | T | 19 | a0001c0001t0001g0199a0001c0001t0005g0099a0001c0002t0001g0045others(16): Show | 19 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.879-997G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339407 | ||||||
| chr8:91339423
|
A | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0013others(68): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.879-981A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339423 | ||||||
| chr8:91339627
|
G | GATTT | 54 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0101others(51): Show | 54 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.879-743_879-740dup others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339627
|
G | GATTTATT others(1): Show |
8 | a0001c0002t0001g0045a0001c0002t0002g0047a0001c0002t0003g0011others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.879-747_879-740dup others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339627
|
G | GATTTATT others(5): Show |
2 | a0001c0001t0001g0199a0001c0002t0001g0112 | 2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.879-751_879-740dup others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339627
|
G | GATTTATT others(9): Show |
1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879-755_879-740dup others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339627
|
GATTT | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0025others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.879-743_879-740del others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339627
|
GATTTATT others(1): Show |
G | 15 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0122others(12): Show | 17 | HG01123.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.879-747_879-740del others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339627
|
GATTTATT others(9): Show |
G | 5 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0064others(2): Show | 5 | HG02132.hp2 NA18989.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.879-755_879-740del others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | |||||
| chr8:91339773
|
T | C | 7 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(4): Show | 7 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.879-631T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339773 | ||||||
| chr8:91340244
|
A | G | 7 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(4): Show | 7 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.879-160A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91340244 | ||||||
| chr8:91340325
|
G | A | 7 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(4): Show | 7 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.879-79G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91340325 | ||||||
| chr8:91340385
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0127a0001c0001t0004g0202 | 3 | HG01261.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.879-19A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91340385 | ||||||
| chr8:91340659
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 145 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.1026+108C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91340659 | ||||||
| chr8:91340988
|
CT | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(76): Show | 80 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1026+450delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 91340988 | |||||
| chr8:91341048
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0023g0104 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1026+497A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341048 | ||||||
| chr8:91341076
|
C | A | 1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1026+525C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341076 | ||||||
| chr8:91341510
|
C | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0168 | 2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.1026+959C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341510 | ||||||
| chr8:91341670
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(51): Show | 56 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1026+1119C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341670 | ||||||
| chr8:91341740
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(10): Show | 15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026+1189A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341740 | ||||||
| chr8:91341965
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1027-1388G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341965 | ||||||
| chr8:91342039
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1027-1314C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342039 | ||||||
| chr8:91342094
|
C | CT | 10 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0060others(7): Show | 10 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-1249dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 91342094 | |||||
| chr8:91342115
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1027-1238A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342115 | ||||||
| chr8:91342130
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0066 | 2 | NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1027-1223T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342130 | ||||||
| chr8:91342445
|
G | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0076a0001c0001t0001g0085others(4): Show | 7 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027-908G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342445 | ||||||
| chr8:91342656
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1027-697C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342656 | ||||||
| chr8:91342693
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(125): Show | 131 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.1027-660G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342693 | ||||||
| chr8:91342821
|
C | T | 2 | a0001c0002t0003g0011a0001c0002t0003g0204 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1027-532C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342821 | ||||||
| chr8:91343311
|
A | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1027-42A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91343311 | ||||||
| chr8:91343808
|
A | C | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1140+342A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91343808 | ||||||
| chr8:91344101
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1140+635T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344101 | ||||||
| chr8:91344137
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1140+671G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344137 | ||||||
| chr8:91344522
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0119 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1140+1056A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344522 | ||||||
| chr8:91344545
|
G | A | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1140+1079G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344545 | ||||||
| chr8:91344977
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(66): Show | 71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+1511C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344977 | ||||||
| chr8:91345023
|
GC | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0072 | 3 | HG03195.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1140+1559delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91345023 | |||||
| chr8:91345107
|
AT | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1140+1653delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91345107 | |||||
| chr8:91345291
|
A | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0001g0137others(4): Show | 7 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+1825A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345291 | ||||||
| chr8:91345512
|
T | A | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1140+2046T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345512 | ||||||
| chr8:91345590
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1140+2124C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345590 | ||||||
| chr8:91345725
|
G | C | 3 | a0001c0001t0001g0030a0003c0009t0011g0143a0004c0011t0014g0022 | 3 | HG01243.hp2 HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1140+2259G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345725 | ||||||
| chr8:91345763
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1140+2297G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345763 | ||||||
| chr8:91345820
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(10): Show | 15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1140+2354G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345820 | ||||||
| chr8:91345823
|
A | C | 1 | a0001c0001t0005g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1140+2357A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345823 | ||||||
| chr8:91345889
|
G | T | 7 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(4): Show | 7 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+2423G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345889 | ||||||
| chr8:91346246
|
A | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0076a0001c0001t0001g0085others(4): Show | 7 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1140+2780A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346246 | ||||||
| chr8:91346344
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(5): Show | 10 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1140+2878C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346344 | ||||||
| chr8:91346501
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(66): Show | 71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+3035T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346501 | ||||||
| chr8:91346531
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(66): Show | 71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+3065G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346531 | ||||||
| chr8:91346545
|
A | G | 13 | a0001c0001t0001g0199a0001c0002t0001g0045a0001c0002t0001g0110others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1140+3079A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346545 | ||||||
| chr8:91346842
|
A | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1140+3376A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346842 | ||||||
| chr8:91346955
|
C | T | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1140+3489C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346955 | ||||||
| chr8:91346982
|
G | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(66): Show | 71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+3516G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346982 | ||||||
| chr8:91347109
|
G | A | 7 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(4): Show | 7 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+3643G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347109 | ||||||
| chr8:91347265
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1140+3799A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347265 | ||||||
| chr8:91347320
|
G | A | 1 | a0005c0010t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1140+3854G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347320 | ||||||
| chr8:91347339
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1140+3873A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347339 | ||||||
| chr8:91347536
|
T | C | 22 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(19): Show | 22 | HG00733.hp2 HG01074.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1140+4070T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347536 | ||||||
| chr8:91347725
|
A | C | 2 | a0001c0001t0001g0101a0001c0001t0021g0206 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1141-4085A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347725 | ||||||
| chr8:91347877
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1141-3933C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347877 | ||||||
| chr8:91347922
|
C | T | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1141-3888C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347922 | ||||||
| chr8:91347965
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(80): Show | 85 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.1141-3845T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347965 | ||||||
| chr8:91348005
|
G | A | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1141-3805G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348005 | ||||||
| chr8:91348086
|
A | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1141-3724A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348086 | ||||||
| chr8:91348138
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0119 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1141-3672A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348138 | ||||||
| chr8:91348168
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(43): Show | 48 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1141-3642T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348168 | ||||||
| chr8:91348348
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0010others(62): Show | 67 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1141-3462G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348348 | ||||||
| chr8:91348389
|
G | A | 18 | a0001c0002t0001g0045a0001c0002t0001g0103a0001c0002t0001g0110others(15): Show | 18 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1141-3421G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348389 | ||||||
| chr8:91348492
|
A | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0119others(12): Show | 17 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1141-3318A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348492 | ||||||
| chr8:91348602
|
T | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0097a0001c0001t0001g0153 | 3 | HG00639.hp1 HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1141-3208T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348602 | ||||||
| chr8:91348719
|
TC | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(72): Show | 77 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1141-3089delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91348719 | |||||
| chr8:91348720
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-3090C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348720 | ||||||
| chr8:91348978
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(64): Show | 69 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1141-2832G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348978 | ||||||
| chr8:91349011
|
A | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-2799A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349011 | ||||||
| chr8:91349054
|
T | C | 1 | a0001c0002t0006g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1141-2756T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349054 | ||||||
| chr8:91349173
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-2637G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349173 | ||||||
| chr8:91349240
|
AC | A | 23 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1141-2567delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91349240 | |||||
| chr8:91349285
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1141-2525G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349285 | ||||||
| chr8:91349569
|
C | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-2241C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349569 | ||||||
| chr8:91350002
|
T | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1141-1808T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350002 | ||||||
| chr8:91350347
|
CT | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0170others(2): Show | 5 | HG01069.hp1 HG01255.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1452delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91350347 | |||||
| chr8:91350359
|
A | T | 9 | a0001c0001t0005g0004a0001c0001t0005g0099a0001c0001t0005g0118others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-1451A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350359 | ||||||
| chr8:91350439
|
GA | G | 42 | a0001c0002t0001g0027a0001c0002t0001g0045a0001c0002t0001g0053others(39): Show | 42 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1141-1362delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91350439 | |||||
| chr8:91350559
|
C | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1141-1251C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350559 | ||||||
| chr8:91350677
|
G | A | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1141-1133G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350677 | ||||||
| chr8:91350799
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1141-1011G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350799 | ||||||
| chr8:91350836
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1141-974T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350836 | ||||||
| chr8:91351162
|
A | G | 47 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1141-648A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351162 | ||||||
| chr8:91351279
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1141-531G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351279 | ||||||
| chr8:91351290
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(20): Show | 25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141-520C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351290 | ||||||
| chr8:91351313
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1141-497C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351313 | ||||||
| chr8:91351321
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1141-489T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351321 | ||||||
| chr8:91351437
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1141-373A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351437 | ||||||
| chr8:91351468
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(20): Show | 25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141-342G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351468 | ||||||
| chr8:91351976
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+89A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91351976 | ||||||
| chr8:91352227
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0017g0192 | 2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1218+340C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352227 | ||||||
| chr8:91352523
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-378A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352523 | ||||||
| chr8:91352589
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1219-312C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352589 | ||||||
| chr8:91352888
|
G | A | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1219-13G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352888 | ||||||
| chr8:91353397
|
A | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02622.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+401A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353397 | ||||||
| chr8:91353538
|
C | T | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1314+542C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353538 | ||||||
| chr8:91353699
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1314+703T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353699 | ||||||
| chr8:91353934
|
A | G | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1314+938A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353934 | ||||||
| chr8:91353965
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1314+969T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353965 | ||||||
| chr8:91354071
|
T | TA | 2 | a0001c0001t0001g0013a0001c0001t0001g0119 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1314+1076dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91354071 | |||||
| chr8:91354282
|
T | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+1286T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354282 | ||||||
| chr8:91354397
|
G | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(69): Show | 74 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1314+1401G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354397 | ||||||
| chr8:91354635
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1314+1639G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354635 | ||||||
| chr8:91354667
|
T | C | 23 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1314+1671T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354667 | ||||||
| chr8:91355440
|
T | C | 23 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1314+2444T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355440 | ||||||
| chr8:91355622
|
G | T | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1314+2626G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355622 | ||||||
| chr8:91355809
|
G | A | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+2813G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355809 | ||||||
| chr8:91355822
|
G | A | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1314+2826G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355822 | ||||||
| chr8:91355836
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0119others(12): Show | 17 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1314+2840C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355836 | ||||||
| chr8:91355870
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02622.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+2874C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355870 | ||||||
| chr8:91355884
|
A | C | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1314+2888A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355884 | ||||||
| chr8:91355891
|
G | C | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1314+2895G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355891 | ||||||
| chr8:91355956
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1314+2960C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355956 | ||||||
| chr8:91355971
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1314+2975T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355971 | ||||||
| chr8:91356063
|
CT | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0119others(12): Show | 17 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1314+3073delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91356063 | |||||
| chr8:91356178
|
G | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1314+3182G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356178 | ||||||
| chr8:91356232
|
T | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG01123.hp2 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1314+3236T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356232 | ||||||
| chr8:91356364
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(78): Show | 83 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.1314+3368G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356364 | ||||||
| chr8:91356432
|
G | A | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+3436G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356432 | ||||||
| chr8:91356434
|
G | A | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+3438G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356434 | ||||||
| chr8:91356437
|
G | A | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1314+3441G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356437 | ||||||
| chr8:91356473
|
T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | HG00733.hp1 HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1314+3477T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356473 | ||||||
| chr8:91356552
|
C | G | 7 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0001g0097others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1314+3556C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356552 | ||||||
| chr8:91356792
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1314+3796A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356792 | ||||||
| chr8:91356839
|
A | G | 3 | a0001c0001t0005g0108a0001c0005t0006g0106a0001c0005t0006g0109 | 3 | HG02970.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1314+3843A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356839 | ||||||
| chr8:91356860
|
T | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1314+3864T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356860 | ||||||
| chr8:91356921
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1314+3925G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356921 | ||||||
| chr8:91357089
|
C | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(9): Show | 14 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1314+4093C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357089 | ||||||
| chr8:91357130
|
T | A | 1 | a0001c0002t0002g0148 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1314+4134T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357130 | ||||||
| chr8:91357493
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+4497A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357493 | ||||||
| chr8:91357553
|
C | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(20): Show | 25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1314+4557C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357553 | ||||||
| chr8:91357675
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(86): Show | 91 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1315-4678G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357675 | ||||||
| chr8:91357791
|
G | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0058 | 2 | NA18989.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1315-4562G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357791 | ||||||
| chr8:91357792
|
C | A | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1315-4561C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357792 | ||||||
| chr8:91357951
|
A | G | 23 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1315-4402A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357951 | ||||||
| chr8:91357958
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(85): Show | 90 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1315-4395T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357958 | ||||||
| chr8:91358032
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315-4321G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358032 | ||||||
| chr8:91358039
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(85): Show | 90 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1315-4314A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358039 | ||||||
| chr8:91358086
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315-4267C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358086 | ||||||
| chr8:91358087
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1315-4266G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358087 | ||||||
| chr8:91358329
|
C | CT | 36 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(33): Show | 38 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1315-4007dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91358329 | |||||
| chr8:91358329
|
CT | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0168a0001c0002t0001g0103others(5): Show | 8 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315-4007delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91358329 | |||||
| chr8:91358415
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0071 | 2 | HG02015.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1315-3938A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358415 | ||||||
| chr8:91358553
|
A | G | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315-3800A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358553 | ||||||
| chr8:91358595
|
G | T | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1315-3758G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358595 | ||||||
| chr8:91358636
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(79): Show | 84 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1315-3717A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358636 | ||||||
| chr8:91358649
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1315-3704G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358649 | ||||||
| chr8:91358811
|
C | T | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315-3542C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358811 | ||||||
| chr8:91358924
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1315-3429C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358924 | ||||||
| chr8:91358985
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1315-3368C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358985 | ||||||
| chr8:91359606
|
A | T | 3 | a0001c0001t0001g0030a0003c0009t0011g0143a0004c0011t0014g0022 | 3 | HG01243.hp2 HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1315-2747A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359606 | ||||||
| chr8:91359727
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1315-2626G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359727 | ||||||
| chr8:91359780
|
T | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315-2573T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359780 | ||||||
| chr8:91359876
|
A | ATG | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1315-2458_1315-245 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | |||||
| chr8:91359876
|
A | ATGTGTG | 7 | a0001c0001t0001g0122a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 8 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315-2462_1315-245 others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | |||||
| chr8:91359876
|
A | ATGTGTGT others(1): Show |
1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1315-2464_1315-245 others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | |||||
| chr8:91359876
|
A | ATGTGTGT others(3): Show |
7 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0200others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1315-2466_1315-245 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | |||||
| chr8:91359876
|
A | G | 1 | a0001c0007t0002g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1315-2477A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359876 | ||||||
| chr8:91359876
|
ATG | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315-2458_1315-245 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | |||||
| chr8:91359895
|
T | TGC | 45 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(42): Show | 45 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1315-2455_1315-245 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359895 | |||||
| chr8:91359895
|
T | TGTGC | 2 | a0001c0002t0015g0024a0001c0002t0022g0023 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1315-2457_1315-245 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359895 | |||||
| chr8:91359897
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0025others(21): Show | 26 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1315-2456C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359897 | ||||||
| chr8:91360257
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1315-2096A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91360257 | ||||||
| chr8:91360306
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1315-2047T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91360306 | ||||||
| chr8:91360487
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1315-1866T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91360487 | ||||||
| chr8:91361567
|
A | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1315-786A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91361567 | ||||||
| chr8:91361815
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(85): Show | 90 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1315-538C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91361815 | ||||||
| chr8:91362080
|
T | G | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1315-273T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91362080 | ||||||
| chr8:91362132
|
TAAA | T | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315-219_1315-217d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91362132 | |||||
| chr8:91362515
|
T | C | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1421+56T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91362515 | ||||||
| chr8:91362525
|
A | G | 23 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1421+66A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91362525 | ||||||
| chr8:91362653
|
G | T | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421+194G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91362653 | ||||||
| chr8:91363413
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1422-59A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91363413 | ||||||
| chr8:91363941
|
GT | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(84): Show | 89 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.1488+420delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 91363941 | |||||
| chr8:91363961
|
T | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1488+423T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91363961 | ||||||
| chr8:91364143
|
C | T | 2 | a0001c0002t0015g0024a0001c0002t0022g0023 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1488+605C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364143 | ||||||
| chr8:91364169
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1488+631G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364169 | ||||||
| chr8:91364495
|
C | T | 1 | a0001c0001t0007g0005 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1488+957C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364495 | ||||||
| chr8:91364958
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0127a0001c0001t0005g0108others(2): Show | 5 | HG01261.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488+1420G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364958 | ||||||
| chr8:91365047
|
C | CTCT | 82 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(79): Show | 84 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1488+1512_1488+151 others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 91365047 | |||||
| chr8:91365133
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1489-1447C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365133 | ||||||
| chr8:91365163
|
AT | A | 23 | a0001c0002t0001g0027a0001c0002t0001g0053a0001c0002t0001g0054others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1489-1409delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 91365163 | |||||
| chr8:91365528
|
G | C | 39 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0032others(36): Show | 39 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1489-1052G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365528 | ||||||
| chr8:91365582
|
G | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1489-998G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365582 | ||||||
| chr8:91365753
|
T | C | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1489-827T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365753 | ||||||
| chr8:91366188
|
T | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1489-392T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366188 | ||||||
| chr8:91366255
|
A | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(20): Show | 25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1489-325A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366255 | ||||||
| chr8:91366354
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1489-226T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366354 | ||||||
| chr8:91366419
|
C | T | 7 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0001g0097others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1489-161C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366419 | ||||||
| chr8:91366554
|
C | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(20): Show | 25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1489-26C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366554 | ||||||
| chr8:91366930
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1626+213G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91366930 | ||||||
| chr8:91367099
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1626+382C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367099 | ||||||
| chr8:91367168
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1626+451C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367168 | ||||||
| chr8:91367259
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1626+542C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367259 | ||||||
| chr8:91367299
|
C | T | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1626+582C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367299 | ||||||
| chr8:91367387
|
C | T | 10 | a0001c0002t0002g0046a0001c0002t0002g0047a0001c0002t0002g0070others(7): Show | 10 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+670C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367387 | ||||||
| chr8:91367488
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1626+771G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367488 | ||||||
| chr8:91367577
|
A | AG | 73 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(70): Show | 75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1626+860_1626+861i others(3): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367577 | ||||||
| chr8:91367639
|
T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1626+922T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367639 | ||||||
| chr8:91367851
|
A | G | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+1134A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367851 | ||||||
| chr8:91367854
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1626+1137G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367854 | ||||||
| chr8:91367943
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1626+1226C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367943 | ||||||
| chr8:91368033
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1626+1316C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368033 | ||||||
| chr8:91368164
|
A | G | 1 | a0001c0002t0012g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1626+1447A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368164 | ||||||
| chr8:91368413
|
G | GT | 15 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(12): Show | 15 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1627-1361dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 91368413 | |||||
| chr8:91368413
|
G | GTT | 72 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(69): Show | 74 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1627-1362_1627-136 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 91368413 | |||||
| chr8:91368425
|
G | T | 1 | a0001c0001t0005g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1627-1360G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368425 | ||||||
| chr8:91368431
|
T | G | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-1354T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368431 | ||||||
| chr8:91368581
|
G | A | 1 | a0003c0009t0011g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1627-1204G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368581 | ||||||
| chr8:91368667
|
C | T | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627-1118C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368667 | ||||||
| chr8:91368944
|
C | A | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1627-841C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368944 | ||||||
| chr8:91368981
|
C | T | 2 | a0002c0003t0001g0135a0002c0003t0001g0136 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1627-804C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368981 | ||||||
| chr8:91368984
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1627-801T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368984 | ||||||
| chr8:91369143
|
C | T | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-642C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91369143 | ||||||
| chr8:91369369
|
GT | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(185): Show | 191 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.1627-403delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 91369369 | |||||
| chr8:91369385
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1627-400T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91369385 | ||||||
| chr8:91369428
|
T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1627-357T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91369428 | ||||||
| chr8:91370079
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1675+246C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370079 | ||||||
| chr8:91370121
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1675+288C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370121 | ||||||
| chr8:91370139
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0018others(15): Show | 19 | HG00642.hp1 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675+306A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370139 | ||||||
| chr8:91370141
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1675+308T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370141 | ||||||
| chr8:91370178
|
C | CT | 75 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(72): Show | 77 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.1675+354dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91370178 | |||||
| chr8:91370197
|
C | CCTT | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(86): Show | 92 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+366_1675+367i others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91370197 | |||||
| chr8:91370579
|
C | T | 55 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(52): Show | 55 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675+746C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370579 | ||||||
| chr8:91370798
|
G | C | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675+965G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370798 | ||||||
| chr8:91371268
|
T | A | 5 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675+1435T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371268 | ||||||
| chr8:91371550
|
TG | T | 24 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(21): Show | 24 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1675+1718delG | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371550 | ||||||
| chr8:91371566
|
A | T | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1675+1733A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371566 | ||||||
| chr8:91371702
|
T | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(188): Show | 194 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1675+1869T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371702 | ||||||
| chr8:91371731
|
T | C | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+1898T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371731 | ||||||
| chr8:91371849
|
C | T | 2 | a0001c0002t0015g0024a0001c0002t0022g0023 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1675+2016C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371849 | ||||||
| chr8:91371901
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1675+2068G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371901 | ||||||
| chr8:91372225
|
G | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1675+2392G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372225 | ||||||
| chr8:91372279
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1675+2446T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372279 | ||||||
| chr8:91372356
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0028others(44): Show | 48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1675+2523A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372356 | ||||||
| chr8:91372365
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG01123.hp2 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1675+2532C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372365 | ||||||
| chr8:91372396
|
A | C | 13 | a0001c0002t0001g0045a0001c0002t0001g0110a0001c0002t0001g0112others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+2563A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372396 | ||||||
| chr8:91372560
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1675+2727T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372560 | ||||||
| chr8:91372650
|
G | A | 6 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(3): Show | 6 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+2817G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372650 | ||||||
| chr8:91372972
|
AT | A | 3 | a0001c0002t0002g0070a0001c0004t0002g0144a0001c0004t0002g0159 | 3 | NA18947.hp2 NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1675+3146delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91372972 | |||||
| chr8:91373120
|
T | G | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675+3287T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373120 | ||||||
| chr8:91373287
|
T | A | 1 | a0001c0002t0003g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1675+3454T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373287 | ||||||
| chr8:91373371
|
G | C | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1675+3538G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373371 | ||||||
| chr8:91373428
|
G | A | 5 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675+3595G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373428 | ||||||
| chr8:91373801
|
A | G | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(7): Show | 10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1675+3968A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373801 | ||||||
| chr8:91374385
|
G | GT | 6 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0160others(3): Show | 6 | HG02055.hp1 NA18989.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+4563dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91374385 | |||||
| chr8:91374385
|
GT | G | 54 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0040others(51): Show | 54 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1675+4563delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91374385 | |||||
| chr8:91374639
|
T | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1675+4806T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91374639 | ||||||
| chr8:91374804
|
A | T | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1675+4971A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91374804 | ||||||
| chr8:91375151
|
T | C | 2 | a0001c0001t0007g0005a0001c0001t0007g0006 | 2 | NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1675+5318T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375151 | ||||||
| chr8:91375261
|
G | GT | 14 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(11): Show | 14 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1675+5432dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91375261 | |||||
| chr8:91375269
|
T | C | 55 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(52): Show | 55 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1675+5436T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375269 | ||||||
| chr8:91375487
|
T | A | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1675+5654T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375487 | ||||||
| chr8:91375636
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1675+5803C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375636 | ||||||
| chr8:91375660
|
GT | G | 41 | a0001c0001t0001g0030a0001c0002t0001g0014a0001c0002t0001g0015others(38): Show | 41 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1675+5841delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91375660 | |||||
| chr8:91375857
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1675+6024C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375857 | ||||||
| chr8:91375907
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1675+6074A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375907 | ||||||
| chr8:91376078
|
G | T | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1675+6245G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91376078 | ||||||
| chr8:91376763
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1675+6930C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91376763 | ||||||
| chr8:91376857
|
A | G | 3 | a0001c0001t0005g0108a0001c0005t0006g0106a0001c0005t0006g0109 | 3 | HG02970.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1675+7024A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91376857 | ||||||
| chr8:91377099
|
G | T | 3 | a0001c0001t0010g0092a0001c0001t0010g0093a0001c0001t0010g0094 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1675+7266G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377099 | ||||||
| chr8:91377197
|
A | T | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1675+7364A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377197 | ||||||
| chr8:91377230
|
G | T | 1 | a0001c0002t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1675+7397G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377230 | ||||||
| chr8:91377284
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1675+7451C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377284 | ||||||
| chr8:91377323
|
C | A | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1675+7490C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377323 | ||||||
| chr8:91377498
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1675+7665G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377498 | ||||||
| chr8:91377655
|
C | G | 41 | a0001c0001t0001g0030a0001c0002t0001g0014a0001c0002t0001g0015others(38): Show | 41 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1675+7822C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377655 | ||||||
| chr8:91377714
|
G | T | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1675+7881G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377714 | ||||||
| chr8:91377789
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1675+7956C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377789 | ||||||
| chr8:91377790
|
G | C | 1 | a0001c0001t0001g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1675+7957G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377790 | ||||||
| chr8:91378298
|
A | C | 4 | a0001c0001t0001g0200a0001c0001t0009g0201a0001c0001t0009g0207others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+8465A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378298 | ||||||
| chr8:91378499
|
AG | A | 14 | a0001c0002t0001g0027a0001c0002t0001g0080a0001c0002t0001g0186others(11): Show | 14 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1675+8668delG | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91378499 | |||||
| chr8:91378561
|
A | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1675+8728A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378561 | ||||||
| chr8:91378779
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0028others(44): Show | 48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1675+8946C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378779 | ||||||
| chr8:91378887
|
C | T | 1 | a0001c0001t0005g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1675+9054C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378887 | ||||||
| chr8:91379061
|
TA | T | 13 | a0001c0002t0001g0027a0001c0002t0001g0080a0001c0002t0001g0186others(10): Show | 13 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+9236delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91379061 | |||||
| chr8:91379224
|
A | G | 2 | a0001c0001t0004g0202a0001c0001t0018g0124 | 2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1675+9391A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379224 | ||||||
| chr8:91379302
|
G | A | 1 | a0001c0002t0015g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1675+9469G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379302 | ||||||
| chr8:91379553
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1675+9720A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379553 | ||||||
| chr8:91379642
|
A | G | 40 | a0001c0001t0001g0030a0001c0002t0001g0014a0001c0002t0001g0015others(37): Show | 40 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-9696A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379642 | ||||||
| chr8:91379723
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-9615A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379723 | ||||||
| chr8:91379883
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1676-9455A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379883 | ||||||
| chr8:91379938
|
A | G | 3 | a0001c0002t0001g0045a0001c0002t0001g0110a0001c0002t0001g0112 | 3 | HG02280.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1676-9400A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379938 | ||||||
| chr8:91379957
|
G | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(188): Show | 194 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1676-9381G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379957 | ||||||
| chr8:91380034
|
T | C | 13 | a0001c0002t0001g0045a0001c0002t0001g0110a0001c0002t0001g0112others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1676-9304T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380034 | ||||||
| chr8:91380198
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1676-9140G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380198 | ||||||
| chr8:91380525
|
T | G | 4 | a0001c0001t0001g0043a0001c0001t0002g0007a0001c0001t0002g0063others(1): Show | 4 | HG02148.hp1 HG02300.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-8813T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380525 | ||||||
| chr8:91380666
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1676-8672A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380666 | ||||||
| chr8:91381020
|
GA | G | 3 | a0001c0002t0001g0045a0001c0002t0001g0110a0001c0002t0001g0112 | 3 | HG02280.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1676-8312delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91381020 | |||||
| chr8:91381330
|
C | A | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1676-8008C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381330 | ||||||
| chr8:91381619
|
A | G | 13 | a0001c0002t0001g0045a0001c0002t0001g0110a0001c0002t0001g0112others(10): Show | 13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1676-7719A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381619 | ||||||
| chr8:91381773
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02015.hp2 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1676-7565C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381773 | ||||||
| chr8:91381969
|
C | G | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1676-7369C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381969 | ||||||
| chr8:91381980
|
G | C | 40 | a0001c0001t0001g0030a0001c0002t0001g0014a0001c0002t0001g0015others(37): Show | 40 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-7358G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381980 | ||||||
| chr8:91382068
|
T | C | 54 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(51): Show | 54 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1676-7270T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382068 | ||||||
| chr8:91382385
|
C | T | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1676-6953C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382385 | ||||||
| chr8:91382851
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1676-6487G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382851 | ||||||
| chr8:91382918
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0119 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1676-6420T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382918 | ||||||
| chr8:91382931
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1676-6407C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382931 | ||||||
| chr8:91383115
|
A | G | 1 | a0001c0002t0008g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1676-6223A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383115 | ||||||
| chr8:91383135
|
C | T | 3 | a0001c0002t0001g0103a0001c0002t0009g0102a0001c0002t0012g0100 | 3 | HG00735.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1676-6203C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383135 | ||||||
| chr8:91383142
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1676-6196C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383142 | ||||||
| chr8:91383233
|
A | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0021g0206 | 3 | HG02145.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1676-6105A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383233 | ||||||
| chr8:91383272
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(11): Show | 14 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1676-6066T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383272 | ||||||
| chr8:91383366
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(11): Show | 14 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1676-5972G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383366 | ||||||
| chr8:91383544
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(11): Show | 14 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1676-5794G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383544 | ||||||
| chr8:91383627
|
C | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(11): Show | 14 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1676-5711C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383627 | ||||||
| chr8:91383862
|
T | C | 14 | a0001c0002t0001g0027a0001c0002t0001g0080a0001c0002t0001g0186others(11): Show | 14 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-5476T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383862 | ||||||
| chr8:91384035
|
G | A | 1 | a0001c0002t0003g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1676-5303G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384035 | ||||||
| chr8:91384051
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(63): Show | 68 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1676-5287G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384051 | ||||||
| chr8:91384193
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1676-5145G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384193 | ||||||
| chr8:91384298
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-5040G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384298 | ||||||
| chr8:91384704
|
G | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(48): Show | 51 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1676-4634G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384704 | ||||||
| chr8:91384719
|
T | C | 2 | a0001c0001t0001g0030a0004c0011t0014g0022 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1676-4619T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384719 | ||||||
| chr8:91384764
|
G | GAGGA | 6 | a0001c0001t0001g0164a0001c0001t0001g0177a0001c0002t0001g0053others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1676-4544_1676-454 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91384764 | |||||
| chr8:91384764
|
GAGGA | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0030others(38): Show | 43 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1676-4544_1676-454 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91384764 | |||||
| chr8:91384769
|
AGGAAGGA others(2): Show |
A | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-4567_1676-455 others(13): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91384769 | |||||
| chr8:91384896
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-4442A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384896 | ||||||
| chr8:91384906
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-4432T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384906 | ||||||
| chr8:91384914
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0025others(112): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1676-4424T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384914 | ||||||
| chr8:91385125
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1676-4213T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385125 | ||||||
| chr8:91385165
|
C | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-4173C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385165 | ||||||
| chr8:91385188
|
A | G | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1676-4150A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385188 | ||||||
| chr8:91385248
|
T | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-4090T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385248 | ||||||
| chr8:91385486
|
C | T | 51 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(48): Show | 51 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1676-3852C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385486 | ||||||
| chr8:91385513
|
C | T | 6 | a0001c0002t0001g0027a0001c0002t0001g0080a0001c0002t0001g0186others(3): Show | 6 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1676-3825C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385513 | ||||||
| chr8:91385628
|
T | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-3710T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385628 | ||||||
| chr8:91386062
|
A | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(48): Show | 51 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1676-3276A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386062 | ||||||
| chr8:91386134
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-3204T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386134 | ||||||
| chr8:91386482
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-2856A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386482 | ||||||
| chr8:91386604
|
C | A | 40 | a0001c0001t0001g0030a0001c0002t0001g0014a0001c0002t0001g0015others(37): Show | 40 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-2734C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386604 | ||||||
| chr8:91386646
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-2692C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386646 | ||||||
| chr8:91387177
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-2161A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387177 | ||||||
| chr8:91387244
|
T | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-2094T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387244 | ||||||
| chr8:91387445
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1676-1893C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387445 | ||||||
| chr8:91387628
|
GAATC | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(60): Show | 65 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1676-1705_1676-170 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91387628 | |||||
| chr8:91387696
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0127 | 2 | HG01261.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1676-1642T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387696 | ||||||
| chr8:91387717
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1676-1621A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387717 | ||||||
| chr8:91387789
|
T | C | 1 | a0005c0010t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1676-1549T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387789 | ||||||
| chr8:91388091
|
T | C | 2 | a0001c0005t0006g0106a0001c0005t0006g0109 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1676-1247T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388091 | ||||||
| chr8:91388118
|
A | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1220A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388118 | ||||||
| chr8:91388153
|
C | A | 2 | a0002c0003t0001g0135a0002c0003t0001g0136 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1676-1185C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388153 | ||||||
| chr8:91388176
|
A | G | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1162A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388176 | ||||||
| chr8:91388217
|
A | G | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1121A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388217 | ||||||
| chr8:91388235
|
G | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1103G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388235 | ||||||
| chr8:91388238
|
C | CTCCTGCC others(109): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0021g0206 | 3 | HG02145.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1676-1066_1676-951 others(119): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91388238 | |||||
| chr8:91388353
|
C | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-985C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388353 | ||||||
| chr8:91388417
|
C | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-921C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388417 | ||||||
| chr8:91388429
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(9): Show | 14 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-909A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388429 | ||||||
| chr8:91388461
|
T | C | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-877T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388461 | ||||||
| chr8:91388576
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1676-762A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388576 | ||||||
| chr8:91388863
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1676-475T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388863 | ||||||
| chr8:91388875
|
A | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-463A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388875 | ||||||
| chr8:91388892
|
A | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02622.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1676-446A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388892 | ||||||
| chr8:91389229
|
A | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0140others(9): Show | 14 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-109A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91389229 | ||||||
| chr8:91389293
|
G | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-45G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91389293 | ||||||
| chr8:91389304
|
C | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-34C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91389304 | ||||||
| chr8:91389642
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1776+204G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389642 | ||||||
| chr8:91389710
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1776+272G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389710 | ||||||
| chr8:91389722
|
G | T | 8 | a0002c0003t0001g0135a0002c0003t0001g0136a0002c0003t0004g0095others(5): Show | 8 | HG00642.hp1 HG02055.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1776+284G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389722 | ||||||
| chr8:91389858
|
T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(186): Show | 192 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.1776+420T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389858 | ||||||
| chr8:91389979
|
A | G | 63 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0039others(60): Show | 63 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1776+541A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389979 | ||||||
| chr8:91390034
|
A | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+596A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390034 | ||||||
| chr8:91390090
|
T | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+652T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390090 | ||||||
| chr8:91390103
|
CA | C | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+666delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390103 | ||||||
| chr8:91390110
|
C | CT | 19 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0122others(16): Show | 19 | HG00735.hp1 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1776+688dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390110 | |||||
| chr8:91390110
|
C | CTT | 5 | a0001c0001t0001g0002a0001c0001t0001g0142a0001c0001t0002g0001others(2): Show | 7 | HG01891.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1776+687_1776+688d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390110 | |||||
| chr8:91390110
|
CT | C | 16 | a0001c0001t0001g0010a0001c0002t0001g0045a0001c0002t0001g0054others(13): Show | 16 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1776+688delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390110 | |||||
| chr8:91390209
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(36): Show | 41 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1776+771T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390209 | ||||||
| chr8:91390308
|
G | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+870G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390308 | ||||||
| chr8:91390359
|
T | C | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+921T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390359 | ||||||
| chr8:91390482
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1776+1044C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390482 | ||||||
| chr8:91390541
|
C | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1103C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390541 | ||||||
| chr8:91390664
|
A | ATACT | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1228_1776+122 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390664 | |||||
| chr8:91390675
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1776+1237C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390675 | ||||||
| chr8:91390679
|
T | C | 6 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1776+1241T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390679 | ||||||
| chr8:91390711
|
A | ATC | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1278_1776+127 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390711 | |||||
| chr8:91390768
|
A | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1330A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390768 | ||||||
| chr8:91390788
|
C | T | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1776+1350C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390788 | ||||||
| chr8:91390794
|
C | T | 1 | a0001c0002t0015g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1776+1356C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390794 | ||||||
| chr8:91390912
|
T | C | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1474T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390912 | ||||||
| chr8:91390920
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0101others(8): Show | 11 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1776+1482G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390920 | ||||||
| chr8:91391062
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1776+1624G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391062 | ||||||
| chr8:91391216
|
T | G | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1778T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391216 | ||||||
| chr8:91391286
|
G | T | 4 | a0001c0001t0001g0200a0001c0001t0009g0201a0001c0001t0009g0207others(1): Show | 4 | HG02896.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1776+1848G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391286 | ||||||
| chr8:91391333
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0021g0206 | 3 | HG02145.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1776+1895T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391333 | ||||||
| chr8:91391363
|
G | T | 2 | a0002c0003t0001g0135a0002c0003t0001g0136 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1776+1925G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391363 | ||||||
| chr8:91391394
|
C | T | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1956C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391394 | ||||||
| chr8:91391609
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02015.hp2 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1776+2171C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391609 | ||||||
| chr8:91391651
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1777-2146C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391651 | ||||||
| chr8:91391682
|
A | G | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-2115A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391682 | ||||||
| chr8:91391751
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0184 | 2 | HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1777-2046A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391751 | ||||||
| chr8:91391802
|
A | AT | 9 | a0001c0002t0001g0045a0001c0002t0002g0046a0001c0002t0002g0047others(6): Show | 9 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1777-1982dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91391802 | |||||
| chr8:91391872
|
A | G | 2 | a0001c0002t0002g0046a0001c0002t0002g0047 | 2 | HG01070.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1777-1925A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391872 | ||||||
| chr8:91391975
|
G | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0030others(10): Show | 13 | HG00642.hp1 HG01243.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1777-1822G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391975 | ||||||
| chr8:91391982
|
T | C | 14 | a0001c0001t0001g0122a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1777-1815T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391982 | ||||||
| chr8:91392098
|
C | T | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1777-1699C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392098 | ||||||
| chr8:91392426
|
G | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-1371G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392426 | ||||||
| chr8:91392530
|
T | C | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1777-1267T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392530 | ||||||
| chr8:91392624
|
C | G | 14 | a0001c0001t0001g0122a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1777-1173C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392624 | ||||||
| chr8:91392656
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1777-1141G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392656 | ||||||
| chr8:91393092
|
C | A | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-705C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393092 | ||||||
| chr8:91393108
|
A | G | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1777-689A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393108 | ||||||
| chr8:91393453
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1777-344T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393453 | ||||||
| chr8:91393497
|
A | C | 2 | a0003c0006t0011g0069a0003c0009t0011g0143 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-300A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393497 | ||||||
| chr8:91393560
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1777-237G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393560 | ||||||
| chr8:91393711
|
A | G | 1 | a0001c0002t0008g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1777-86A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393711 | ||||||
| chr8:91393793
|
C | T | 11 | a0001c0002t0001g0045a0001c0002t0002g0046a0001c0002t0002g0047others(8): Show | 11 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1777-4C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393793 | ||||||
| chr8:91393874
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1831+23C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 17/18 | chr8 | 91393874 | ||||||
| chr8:91394141
|
A | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1935+102A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | chr8 | 91394141 | ||||||
| chr8:91394208
|
CT | C | 18 | a0001c0001t0001g0043a0001c0001t0002g0001a0001c0001t0002g0007others(15): Show | 19 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1935+176delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 91394208 | |||||
| chr8:91394606
|
C | T | 2 | a0001c0001t0001g0060a0001c0002t0001g0045 | 2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1936-456C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | chr8 | 91394606 | ||||||
| chr8:91394931
|
T | A | 6 | a0001c0001t0004g0188a0001c0001t0004g0202a0001c0002t0004g0203others(3): Show | 6 | HG00642.hp1 HG00738.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-131T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | chr8 | 91394931 |