| geneid | 9497 |
|---|---|
| ensemblid | ENSG00000033867.18 |
| hgncid | 11033 |
| symbol | SLC4A7 |
| name | solute carrier family 4 member 7 |
| refseq_nuc | NM_001321103.2 |
| refseq_prot | NP_001308032.1 |
| ensembl_nuc | ENST00000454389.6 |
| ensembl_prot | ENSP00000390394.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 27372723 |
| end | 27484384 |
| strand | - |
| ver | v1.2 |
| region | chr3:27372723-27484384 |
| region5000 | chr3:27367723-27489384 |
| regionname0 | SLC4A7_chr3_27372723_27484384 |
| regionname5000 | SLC4A7_chr3_27367723_27489384 |
| 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 | 1259 | 232 | 74 | 43 | 68 | 12 | 34 | 57 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002 | 0/1 | 1259 | 35 | 3 | 11 | 11 | 4 | 5 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0003 | 0/0 | 1259 | 17 | 0 | 0 | 16 | 0 | 1 | 13 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0004 | 0/0 | 1259 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0005 | 0/0 | 1259 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0006 | 0/0 | 1259 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0007 | 0/0 | 1259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0008 | 0/0 | 1259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0009 | 0/0 | 1259 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0010 | 0/0 | 1259 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3780 | 148 | 39 | 23 | 56 | 4 | 26 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0002 | 0/0 | 3780 | 35 | 16 | 3 | 12 | 3 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0003 | 0/1 | 3780 | 34 | 3 | 11 | 11 | 3 | 5 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0004 | 1/0 | 3780 | 31 | 16 | 7 | 0 | 0 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0005 | 0/0 | 3780 | 17 | 0 | 0 | 16 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0006 | 0/0 | 3780 | 14 | 0 | 9 | 0 | 5 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0007 | 0/0 | 3780 | 11 | 8 | 3 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0008 | 0/0 | 3780 | 2 | 1 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0009 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0010 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0011 | 0/0 | 3780 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0012 | 0/0 | 3780 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0013 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0014 | 0/0 | 3780 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0015 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0016 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0017 | 0/0 | 3780 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| c0018 | 0/0 | 3780 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4301 | 100 | 21 | 17 | 39 | 5 | 17 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0002 | 0/0 | 4301 | 35 | 5 | 10 | 11 | 3 | 6 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0003 | 0/0 | 4300 | 32 | 0 | 13 | 11 | 1 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0004 | 0/0 | 4300 | 25 | 16 | 2 | 7 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0005 | 0/0 | 4296 | 20 | 2 | 1 | 17 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0006 | 0/0 | 4301 | 16 | 4 | 5 | 0 | 0 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0007 | 0/0 | 4301 | 10 | 9 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0008 | 0/0 | 4302 | 10 | 6 | 3 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0009 | 0/0 | 4301 | 9 | 9 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0010 | 0/0 | 4300 | 8 | 6 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0011 | 0/0 | 4300 | 7 | 0 | 2 | 0 | 4 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0012 | 0/0 | 4301 | 5 | 0 | 0 | 5 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0013 | 0/0 | 4301 | 4 | 2 | 2 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0014 | 0/0 | 4297 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0015 | 0/0 | 4301 | 2 | 0 | 0 | 0 | 2 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0016 | 0/0 | 4301 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0017 | 1/0 | 4300 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0018 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0019 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0020 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0021 | 0/0 | 4301 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0022 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0023 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0024 | 0/0 | 4301 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0025 | 0/0 | 4301 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0026 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0027 | 0/0 | 4301 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0028 | 0/0 | 4301 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0029 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0030 | 0/0 | 4300 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| t0031 | 0/0 | 4297 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| 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 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3780 | 148 | 39 | 23 | 56 | 4 | 26 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0002 | 0/0 | 3780 | 35 | 16 | 3 | 12 | 3 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0004 | 1/0 | 3780 | 31 | 16 | 7 | 0 | 0 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0006 | 0/0 | 3780 | 14 | 0 | 9 | 0 | 5 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0009 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0013 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0016 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0018 | 0/0 | 3780 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002c0003 | 0/1 | 3780 | 34 | 3 | 11 | 11 | 3 | 5 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002c0012 | 0/0 | 3780 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0003c0005 | 0/0 | 3780 | 17 | 0 | 0 | 16 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0004c0007 | 0/0 | 3780 | 11 | 8 | 3 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0005c0008 | 0/0 | 3780 | 2 | 1 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0006c0011 | 0/0 | 3780 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0007c0010 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0008c0015 | 0/0 | 3780 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0009c0014 | 0/0 | 3780 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0010c0017 | 0/0 | 3780 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8080 | 82 | 20 | 8 | 38 | 0 | 16 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0002 | 0/0 | 8080 | 2 | 1 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0003 | 0/0 | 8079 | 32 | 0 | 13 | 11 | 1 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0005 | 0/0 | 8075 | 4 | 2 | 1 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0007 | 0/0 | 8080 | 9 | 8 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0008 | 0/0 | 8081 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0010 | 0/0 | 8079 | 8 | 6 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0011 | 0/0 | 8079 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0014 | 0/0 | 8076 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0015 | 0/0 | 8080 | 2 | 0 | 0 | 0 | 2 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0018 | 0/0 | 8075 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0020 | 0/0 | 8079 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0024 | 0/0 | 8080 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0001t0030 | 0/0 | 8079 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0002t0004 | 0/0 | 8079 | 23 | 15 | 1 | 7 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0002t0011 | 0/0 | 8079 | 6 | 0 | 2 | 0 | 3 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0002t0012 | 0/0 | 8080 | 5 | 0 | 0 | 5 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0002t0026 | 0/0 | 8079 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0004t0006 | 0/0 | 8080 | 16 | 4 | 5 | 0 | 0 | 7 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0004t0009 | 0/0 | 8080 | 9 | 9 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0004t0013 | 0/0 | 8080 | 4 | 2 | 2 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0004t0016 | 0/0 | 8080 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0004t0017 | 1/0 | 8079 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0006t0001 | 0/0 | 8080 | 14 | 0 | 9 | 0 | 5 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0009t0019 | 0/0 | 8079 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0013t0029 | 0/0 | 8079 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0016t0007 | 0/0 | 8080 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0001c0018t0004 | 0/0 | 8079 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002c0003t0001 | 0/1 | 8080 | 2 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002c0003t0002 | 0/0 | 8080 | 31 | 3 | 10 | 11 | 3 | 4 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002c0003t0027 | 0/0 | 8080 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0002c0012t0028 | 0/0 | 8080 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0003c0005t0005 | 0/0 | 8075 | 16 | 0 | 0 | 16 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0003c0005t0031 | 0/0 | 8076 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0004c0007t0001 | 0/0 | 8080 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0004c0007t0008 | 0/0 | 8081 | 9 | 6 | 3 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0004c0007t0023 | 0/0 | 8081 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0005c0008t0002 | 0/0 | 8080 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0005c0008t0025 | 0/0 | 8080 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0006c0011t0021 | 0/0 | 8080 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0007c0010t0004 | 0/0 | 8079 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0008c0015t0022 | 0/0 | 8079 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0009c0014t0001 | 0/0 | 8080 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| a0010c0017t0002 | 0/0 | 8080 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | copy fasta | chr3 | 27367723 | 27489384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0014g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0015g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0020g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0024g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0001t0030g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0011g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0011g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0011g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0011g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0012g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0012g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0002t0026g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0013g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0013g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0016g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0004t0017g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0006t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0009t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0013t0029g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0016t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0001c0018t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0003t0027g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0002c0012t0028g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0003c0005t0031g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0004c0007t0023g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0005c0008t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0005c0008t0025g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0006c0011t0021g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0007c0010t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0008c0015t0022g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0009c0014t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| a0010c0017t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0011 | g0056 | EUR | GBR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0158 | EUR | GBR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0120 | EUR | FIN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00280 | hp2 | a0001 | c0006 | t0001 | g0234 | EUR | FIN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00323 | hp1 | a0001 | c0002 | t0011 | g0054 | EUR | FIN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00323 | hp2 | a0001 | c0006 | t0001 | g0214 | EUR | FIN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00408 | hp2 | a0003 | c0005 | t0005 | g0145 | EAS | CHS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00639 | hp1 | a0004 | c0007 | t0008 | g0262 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00639 | hp2 | a0001 | c0006 | t0001 | g0213 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00642 | hp2 | a0001 | c0004 | t0006 | g0012 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | CHS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00735 | hp1 | a0001 | c0018 | t0004 | g0074 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0178 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00738 | hp2 | a0001 | c0004 | t0006 | g0019 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00741 | hp1 | a0001 | c0002 | t0011 | g0059 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01070 | hp1 | a0001 | c0006 | t0001 | g0193 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0152 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01074 | hp1 | a0001 | c0002 | t0011 | g0053 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01074 | hp2 | a0002 | c0003 | t0002 | g0180 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01099 | hp1 | a0001 | c0006 | t0001 | g0223 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01099 | hp2 | a0001 | c0004 | t0006 | g0014 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01106 | hp1 | a0006 | c0011 | t0021 | g0057 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01106 | hp2 | a0001 | c0004 | t0006 | g0020 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0171 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01167 | hp1 | a0004 | c0007 | t0008 | g0252 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01167 | hp2 | a0001 | c0006 | t0001 | g0207 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01169 | hp1 | a0001 | c0006 | t0001 | g0220 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01169 | hp2 | a0004 | c0007 | t0008 | g0256 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01192 | hp1 | a0002 | c0003 | t0027 | g0184 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01192 | hp2 | a0001 | c0006 | t0001 | g0249 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01243 | hp2 | a0001 | c0004 | t0013 | g0010 | AMR | PUR | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0169 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01257 | hp2 | a0002 | c0003 | t0002 | g0168 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0182 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01261 | hp1 | a0001 | c0004 | t0006 | g0017 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0183 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0161 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0086 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01496 | hp1 | a0001 | c0006 | t0001 | g0219 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0267 | AMR | CLM | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01515 | hp1 | a0001 | c0006 | t0001 | g0230 | EUR | IBS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0179 | EUR | IBS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01516 | hp1 | a0001 | c0006 | t0001 | g0005 | EUR | IBS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01516 | hp2 | a0001 | c0001 | t0015 | g0088 | EUR | IBS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0177 | EUR | IBS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01517 | hp2 | a0001 | c0006 | t0001 | g0005 | EUR | IBS | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01884 | hp1 | a0001 | c0004 | t0009 | g0030 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0100 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0176 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01934 | hp2 | a0001 | c0004 | t0013 | g0023 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01943 | hp1 | a0001 | c0006 | t0001 | g0209 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG01981 | hp2 | a0001 | c0006 | t0001 | g0225 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02027 | hp1 | a0003 | c0005 | t0005 | g0148 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02040 | hp1 | a0002 | c0003 | t0002 | g0157 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02055 | hp1 | a0001 | c0004 | t0006 | g0025 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0167 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02071 | hp1 | a0003 | c0005 | t0005 | g0144 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02071 | hp2 | a0002 | c0003 | t0002 | g0165 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0149 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02083 | hp1 | a0002 | c0003 | t0002 | g0166 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02129 | hp1 | a0002 | c0003 | t0002 | g0170 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0075 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02145 | hp2 | a0004 | c0007 | t0008 | g0260 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | CDX | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02257 | hp1 | a0001 | c0009 | t0019 | g0055 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02258 | hp1 | a0001 | c0016 | t0007 | g0043 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02280 | hp2 | a0001 | c0004 | t0006 | g0028 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0160 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0036 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02602 | hp1 | a0002 | c0003 | t0002 | g0188 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02615 | hp2 | a0004 | c0007 | t0008 | g0257 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02683 | hp1 | a0001 | c0004 | t0006 | g0016 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0063 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02735 | hp2 | a0005 | c0008 | t0025 | g0155 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0201 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02818 | hp1 | a0001 | c0013 | t0029 | g0251 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02818 | hp2 | a0004 | c0007 | t0008 | g0255 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0060 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0061 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0112 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0064 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02965 | hp1 | a0004 | c0007 | t0008 | g0253 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0083 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02976 | hp1 | a0001 | c0001 | t0010 | g0099 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03017 | hp2 | a0001 | c0002 | t0011 | g0048 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03041 | hp1 | a0005 | c0008 | t0002 | g0153 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03041 | hp2 | a0001 | c0004 | t0013 | g0008 | AFR | GWD | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03098 | hp2 | a0001 | c0004 | t0006 | g0024 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03139 | hp1 | a0004 | c0007 | t0001 | g0254 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03195 | hp1 | a0001 | c0004 | t0009 | g0033 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03195 | hp2 | a0004 | c0007 | t0023 | g0259 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03209 | hp1 | a0008 | c0015 | t0022 | g0037 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0082 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03225 | hp2 | a0001 | c0004 | t0009 | g0001 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03239 | hp1 | a0001 | c0004 | t0006 | g0018 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0062 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03486 | hp1 | a0001 | c0004 | t0009 | g0001 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03486 | hp2 | a0004 | c0007 | t0008 | g0258 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0173 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03490 | hp2 | a0001 | c0001 | t0030 | g0114 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0174 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03516 | hp2 | a0007 | c0010 | t0004 | g0049 | AFR | ESN | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03579 | hp1 | a0001 | c0004 | t0009 | g0027 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03654 | hp2 | a0002 | c0003 | t0002 | g0151 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03688 | hp2 | a0001 | c0004 | t0006 | g0015 | SAS | STU | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03710 | hp1 | a0001 | c0004 | t0006 | g0007 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03831 | hp1 | a0002 | c0003 | t0001 | g0162 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03834 | hp2 | a0010 | c0017 | t0002 | g0156 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03927 | hp1 | a0001 | c0004 | t0006 | g0011 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | STU | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG04184 | hp1 | a0001 | c0004 | t0006 | g0022 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG04184 | hp2 | a0003 | c0005 | t0031 | g0141 | SAS | BEB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG04228 | hp1 | a0001 | c0004 | t0006 | g0021 | SAS | STU | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18522 | hp1 | a0001 | c0004 | t0009 | g0031 | AFR | YRI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0069 | AFR | YRI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0119 | AFR | YRI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18940 | hp2 | a0002 | c0003 | t0002 | g0185 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0186 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18950 | hp1 | a0003 | c0005 | t0005 | g0147 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18953 | hp1 | a0001 | c0001 | t0014 | g0244 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18953 | hp2 | a0001 | c0002 | t0012 | g0066 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18956 | hp1 | a0001 | c0002 | t0012 | g0076 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18957 | hp2 | a0003 | c0005 | t0005 | g0139 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0113 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18960 | hp1 | a0002 | c0003 | t0002 | g0181 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18961 | hp1 | a0003 | c0005 | t0005 | g0146 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18961 | hp2 | a0002 | c0003 | t0002 | g0163 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18963 | hp2 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18968 | hp2 | a0002 | c0003 | t0002 | g0164 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18980 | hp1 | a0003 | c0005 | t0005 | g0003 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18982 | hp1 | a0003 | c0005 | t0005 | g0140 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18984 | hp1 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18986 | hp1 | a0003 | c0005 | t0005 | g0142 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18989 | hp2 | a0001 | c0002 | t0012 | g0050 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18993 | hp1 | a0003 | c0005 | t0005 | g0134 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18998 | hp1 | a0003 | c0005 | t0005 | g0143 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18998 | hp2 | a0009 | c0014 | t0001 | g0248 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19007 | hp1 | a0001 | c0002 | t0012 | g0067 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19007 | hp2 | a0003 | c0005 | t0005 | g0002 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19010 | hp2 | a0003 | c0005 | t0005 | g0003 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19011 | hp1 | a0001 | c0001 | t0014 | g0226 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19011 | hp2 | a0001 | c0002 | t0012 | g0051 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0035 | AFR | LWK | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19030 | hp2 | a0001 | c0004 | t0016 | g0006 | AFR | LWK | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0175 | AFR | LWK | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0065 | AFR | LWK | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0172 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19056 | hp2 | a0003 | c0005 | t0005 | g0138 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19058 | hp1 | a0001 | c0001 | t0014 | g0250 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19058 | hp2 | a0003 | c0005 | t0005 | g0002 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19066 | hp2 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19070 | hp2 | a0001 | c0001 | t0024 | g0202 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19077 | hp1 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19086 | hp1 | a0002 | c0003 | t0002 | g0187 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19087 | hp2 | a0001 | c0001 | t0010 | g0105 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19091 | hp2 | a0003 | c0005 | t0005 | g0133 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | YRI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ASW | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0070 | AFR | ASW | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20752 | hp1 | a0002 | c0012 | t0028 | g0154 | EUR | TSI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20752 | hp2 | a0001 | c0002 | t0011 | g0058 | EUR | TSI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20805 | hp1 | a0001 | c0001 | t0015 | g0087 | EUR | TSI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20805 | hp2 | a0001 | c0001 | t0011 | g0052 | EUR | TSI | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0072 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02109 | hp2 | a0004 | c0007 | t0008 | g0261 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02486 | hp1 | a0001 | c0004 | t0013 | g0009 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02486 | hp2 | a0001 | c0004 | t0009 | g0034 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02559 | hp1 | a0001 | c0004 | t0009 | g0032 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03471 | hp1 | a0001 | c0002 | t0026 | g0283 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | MSL | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0107 | AFR | USA | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| HG06807 | hp2 | a0001 | c0004 | t0006 | g0029 | AFR | USA | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA18955 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20300 | hp1 | a0001 | c0004 | t0009 | g0026 | AFR | USA | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | USA | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0068 | AFR | LWK | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0084 | AFR | LWK | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0159 | REF | REF | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0017 | g0013 | REF | REF | SLC4A7_chr3_27367723_27489384 | SLC4A7 | chr3 | 27367723 | 27489384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:27395106
|
G | A | 1 | a0005 | 2 | HG02735.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.2713C>T | p.Pro905Ser | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 19/26 | 2971/8079 | 2713/3780 | 905/1259 | chr3 | 27395106 | ||
| chr3:27395109
|
G | A | 1 | a0010 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2710C>T | p.His904Tyr | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 19/26 | 2968/8079 | 2710/3780 | 904/1259 | chr3 | 27395109 | ||
| chr3:27398299
|
G | C | 1 | a0008 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2482C>G | p.Pro828Ala | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 17/26 | 2740/8079 | 2482/3780 | 828/1259 | chr3 | 27398299 | ||
| chr3:27403166
|
T | C | 1 | a0003 | 17 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(14): Show |
missense_variant | MODERATE | c.2294A>G | p.Asn765Ser | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/26 | 2552/8079 | 2294/3780 | 765/1259 | chr3 | 27403166 | ||
| chr3:27411709
|
G | T | 1 | a0009 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.1699C>A | p.Pro567Thr | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/26 | 1957/8079 | 1699/3780 | 567/1259 | chr3 | 27411709 | ||
| chr3:27431445
|
C | T | 3 | a0002a0005a0010 | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
missense_variant | MODERATE | c.1003G>A | p.Glu335Lys | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/26 | 1261/8079 | 1003/3780 | 335/1259 | chr3 | 27431445 | ||
| chr3:27431469
|
G | A | 1 | a0007 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.979C>T | p.Arg327Cys | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/26 | 1237/8079 | 979/3780 | 327/1259 | chr3 | 27431469 | ||
| chr3:27431665
|
T | A | 1 | a0004 | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
missense_variant | MODERATE | c.783A>T | p.Glu261Asp | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/26 | 1041/8079 | 783/3780 | 261/1259 | chr3 | 27431665 | ||
| chr3:27433993
|
G | C | 1 | a0006 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.701C>G | p.Thr234Ser | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/26 | 959/8079 | 701/3780 | 234/1259 | chr3 | 27433993 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:27383227
|
A | G | 17 | a0001c0001a0001c0002a0001c0006others(14): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
synonymous_variant | LOW | c.3516T>C | p.Asp1172Asp | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/26 | 3774/8079 | 3516/3780 | 1172/1259 | chr3 | 27383227 | ||
| chr3:27395104
|
T | C | 1 | a0001c0009 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.2715A>G | p.Pro905Pro | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 19/26 | 2973/8079 | 2715/3780 | 905/1259 | chr3 | 27395104 | ||
| chr3:27400845
|
G | A | 3 | a0002c0003a0005c0008a0010c0017 | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
synonymous_variant | LOW | c.2346C>T | p.Asn782Asn | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/26 | 2604/8079 | 2346/3780 | 782/1259 | chr3 | 27400845 | ||
| chr3:27421684
|
T | C | 1 | a0001c0016 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1362A>G | p.Ala454Ala | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/26 | 1620/8079 | 1362/3780 | 454/1259 | chr3 | 27421684 | ||
| chr3:27421738
|
C | T | 1 | a0001c0006 | 14 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
synonymous_variant | LOW | c.1308G>A | p.Glu436Glu | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/26 | 1566/8079 | 1308/3780 | 436/1259 | chr3 | 27421738 | ||
| chr3:27431575
|
A | G | 6 | a0001c0013a0002c0003a0002c0012others(3): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
synonymous_variant | LOW | c.873T>C | p.Leu291Leu | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/26 | 1131/8079 | 873/3780 | 291/1259 | chr3 | 27431575 | ||
| chr3:27437408
|
A | G | 5 | a0001c0002a0001c0009a0001c0018others(2): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
synonymous_variant | LOW | c.408T>C | p.Tyr136Tyr | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/26 | 666/8079 | 408/3780 | 136/1259 | chr3 | 27437408 | ||
| chr3:27448703
|
T | C | 2 | a0002c0003a0010c0017 | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
synonymous_variant | LOW | c.237A>G | p.Arg79Arg | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/26 | 495/8079 | 237/3780 | 79/1259 | chr3 | 27448703 | ||
| chr3:27452454
|
T | C | 1 | a0001c0018 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.105A>G | p.Ser35Ser | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/26 | 363/8079 | 105/3780 | 35/1259 | chr3 | 27452454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:27372807
|
T | A | 1 | a0002c0003t0027 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3957A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3957 | chr3 | 27372807 | |||||
| chr3:27372822
|
T | C | 1 | a0001c0013t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3942A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3942 | chr3 | 27372822 | |||||
| chr3:27372840
|
T | C | 1 | a0001c0009t0019 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3924A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3924 | chr3 | 27372840 | |||||
| chr3:27373032
|
G | A | 1 | a0001c0013t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3732C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3732 | chr3 | 27373032 | |||||
| chr3:27373070
|
G | GA | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(23): Show | 211 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*3693dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3693 | chr3 | 27373070 | |||||
| chr3:27373070
|
G | GAA | 4 | a0001c0001t0008a0003c0005t0031a0004c0007t0008others(1): Show | 12 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3692_*3693dupTT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3693 | chr3 | 27373070 | |||||
| chr3:27373123
|
C | T | 2 | a0001c0001t0007a0001c0016t0007 | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3641G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3641 | chr3 | 27373123 | |||||
| chr3:27373150
|
AAAAAC | A | 4 | a0001c0001t0005a0001c0001t0018a0003c0005t0005others(1): Show | 22 | HG00408.hp2 HG01496.hp2 HG02027.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3609_*3613delGTTT others(1): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3609 | chr3 | 27373150 | |||||
| chr3:27373220
|
A | T | 1 | a0001c0001t0024 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3544T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3544 | chr3 | 27373220 | |||||
| chr3:27373404
|
T | C | 1 | a0001c0013t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3360A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3360 | chr3 | 27373404 | |||||
| chr3:27373477
|
A | T | 1 | a0005c0008t0025 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3287T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3287 | chr3 | 27373477 | |||||
| chr3:27373696
|
C | A | 1 | a0004c0007t0023 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3068G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 3068 | chr3 | 27373696 | |||||
| chr3:27373922
|
C | T | 1 | a0001c0001t0030 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2842G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 2842 | chr3 | 27373922 | |||||
| chr3:27374195
|
G | A | 1 | a0002c0003t0027 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2569C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 2569 | chr3 | 27374195 | |||||
| chr3:27374310
|
G | C | 1 | a0002c0003t0027 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2454C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 2454 | chr3 | 27374310 | |||||
| chr3:27374522
|
C | T | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(16): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2242G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 2242 | chr3 | 27374522 | |||||
| chr3:27374756
|
AAAGT | A | 1 | a0001c0001t0014 | 3 | NA18953.hp1 NA19011.hp1 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2004_*2007delACTT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 2004 | chr3 | 27374756 | |||||
| chr3:27374842
|
T | C | 3 | a0001c0001t0020a0004c0007t0023a0008c0015t0022 | 3 | HG02572.hp2 HG03195.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1922A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 1922 | chr3 | 27374842 | |||||
| chr3:27375239
|
T | C | 5 | a0001c0001t0003a0001c0001t0011a0001c0001t0030others(2): Show | 41 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1525A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 1525 | chr3 | 27375239 | |||||
| chr3:27375461
|
C | T | 1 | a0004c0007t0023 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1303G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 1303 | chr3 | 27375461 | |||||
| chr3:27375508
|
T | C | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(18): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1256A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 1256 | chr3 | 27375508 | |||||
| chr3:27375627
|
G | C | 1 | a0001c0013t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1137C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 1137 | chr3 | 27375627 | |||||
| chr3:27375688
|
T | C | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(3): Show | 49 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1076A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 1076 | chr3 | 27375688 | |||||
| chr3:27376110
|
T | C | 5 | a0001c0001t0005a0001c0001t0018a0001c0004t0009others(2): Show | 31 | HG00408.hp2 HG01496.hp2 HG01884.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*654A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 654 | chr3 | 27376110 | |||||
| chr3:27376240
|
C | T | 3 | a0001c0001t0007a0001c0004t0016a0001c0016t0007 | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 524 | chr3 | 27376240 | |||||
| chr3:27376444
|
C | G | 2 | a0001c0004t0013a0001c0004t0016 | 5 | HG01243.hp2 HG01934.hp2 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*320G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 320 | chr3 | 27376444 | |||||
| chr3:27376557
|
G | T | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 207 | chr3 | 27376557 | |||||
| chr3:27376691
|
T | C | 1 | a0008c0015t0022 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 26/26 | 73 | chr3 | 27376691 | |||||
| chr3:27484198
|
C | T | 1 | a0001c0001t0015 | 2 | HG01516.hp2 NA20805.hp1 |
5_prime_UTR_variant | MODIFIER | c.-72G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/26 | 72 | chr3 | 27484198 | |||||
| chr3:27484217
|
C | T | 12 | a0001c0001t0007a0001c0001t0011a0001c0001t0020others(9): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-91G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/26 | 91 | chr3 | 27484217 | |||||
| chr3:27484241
|
G | T | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-115C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/26 | 115 | chr3 | 27484241 | |||||
| chr3:27484340
|
T | C | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
5_prime_UTR_variant | MODIFIER | c.-214A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/26 | 214 | chr3 | 27484340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:27376930
|
C | T | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3699-85G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27376930 | ||||||
| chr3:27377301
|
C | G | 1 | a0001c0004t0016g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3699-456G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377301 | ||||||
| chr3:27377371
|
T | C | 39 | a0001c0004t0006g0018a0001c0013t0029g0251a0002c0003t0001g0159others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.3699-526A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377371 | ||||||
| chr3:27377405
|
T | C | 50 | a0001c0004t0006g0018a0001c0013t0029g0251a0002c0003t0001g0159others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3699-560A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377405 | ||||||
| chr3:27377433
|
C | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(79): Show | 84 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.3699-588G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377433 | ||||||
| chr3:27377673
|
C | T | 1 | a0001c0004t0006g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3699-828G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377673 | ||||||
| chr3:27377818
|
A | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3699-973T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377818 | ||||||
| chr3:27377901
|
T | C | 1 | a0001c0001t0003g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3699-1056A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27377901 | ||||||
| chr3:27378266
|
A | C | 21 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(18): Show | 21 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3698+983T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378266 | ||||||
| chr3:27378377
|
C | T | 37 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(34): Show | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.3698+872G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378377 | ||||||
| chr3:27378383
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0293 | 2 | NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.3698+866A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378383 | ||||||
| chr3:27378554
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3698+695T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378554 | ||||||
| chr3:27378650
|
T | G | 1 | a0001c0001t0001g0292 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3698+599A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378650 | ||||||
| chr3:27378708
|
C | G | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3698+541G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378708 | ||||||
| chr3:27378933
|
C | T | 1 | a0001c0004t0006g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3698+316G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378933 | ||||||
| chr3:27378985
|
G | GTGACCTC others(9): Show |
1 | a0007c0010t0004g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3698+248_3698+263d others(18): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 25/25 | chr3 | 27378985 | ||||||
| chr3:27379525
|
C | T | 1 | a0002c0003t0002g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3591-169G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379525 | ||||||
| chr3:27379533
|
G | A | 46 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(43): Show | 46 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.3591-177C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379533 | ||||||
| chr3:27379534
|
G | A | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3591-178C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379534 | ||||||
| chr3:27379710
|
C | CA | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.3591-355dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379710 | ||||||
| chr3:27379814
|
T | C | 1 | a0002c0003t0002g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3591-458A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379814 | ||||||
| chr3:27379898
|
A | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3591-542T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379898 | ||||||
| chr3:27379918
|
C | G | 1 | a0001c0001t0003g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3591-562G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379918 | ||||||
| chr3:27379936
|
C | T | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.3591-580G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379936 | ||||||
| chr3:27379953
|
T | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0235 | 2 | HG00408.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.3591-597A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379953 | ||||||
| chr3:27379953
|
T | C | 1 | a0006c0011t0021g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3591-597A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379953 | ||||||
| chr3:27379966
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(78): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.3591-610G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379966 | ||||||
| chr3:27379982
|
A | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0235 | 2 | HG00408.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.3591-626T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27379982 | ||||||
| chr3:27380024
|
G | A | 1 | a0004c0007t0008g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3591-668C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380024 | ||||||
| chr3:27380030
|
C | T | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3591-674G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380030 | ||||||
| chr3:27380042
|
C | T | 2 | a0001c0002t0004g0075a0007c0010t0004g0049 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3591-686G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380042 | ||||||
| chr3:27380047
|
G | A | 1 | a0001c0004t0009g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3591-691C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380047 | ||||||
| chr3:27380080
|
G | A | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.3591-724C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380080 | ||||||
| chr3:27380163
|
C | A | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.3591-807G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380163 | ||||||
| chr3:27380260
|
T | C | 21 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(18): Show | 21 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3591-904A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380260 | ||||||
| chr3:27380285
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3591-929G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380285 | ||||||
| chr3:27380314
|
TA | T | 37 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(34): Show | 37 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.3591-959delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380314 | ||||||
| chr3:27380314
|
TAA | T | 217 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(214): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.3591-960_3591-959d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380314 | ||||||
| chr3:27380314
|
TAAA | T | 12 | a0001c0001t0001g0192a0001c0001t0001g0242a0001c0001t0001g0284others(9): Show | 12 | HG01169.hp1 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.3591-961_3591-959d others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380314 | ||||||
| chr3:27380343
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3591-987G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380343 | ||||||
| chr3:27380451
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3591-1095T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380451 | ||||||
| chr3:27380699
|
G | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01109.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3591-1343C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380699 | ||||||
| chr3:27380745
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.3591-1389T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380745 | ||||||
| chr3:27380784
|
C | G | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.3591-1428G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380784 | ||||||
| chr3:27380829
|
C | A | 2 | a0002c0003t0002g0164a0002c0003t0002g0165 | 2 | HG02071.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.3591-1473G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380829 | ||||||
| chr3:27380887
|
C | G | 50 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.3591-1531G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380887 | ||||||
| chr3:27380984
|
T | A | 1 | a0001c0002t0004g0085 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3591-1628A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27380984 | ||||||
| chr3:27381230
|
A | G | 21 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(18): Show | 21 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3591-1874T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381230 | ||||||
| chr3:27381451
|
C | T | 4 | a0001c0004t0009g0001a0001c0004t0009g0032a0001c0004t0009g0033others(1): Show | 5 | HG02486.hp2 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3590+1702G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381451 | ||||||
| chr3:27381491
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3590+1662G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381491 | ||||||
| chr3:27381530
|
ACAT | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3590+1620_3590+162 others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381530 | ||||||
| chr3:27381531
|
C | T | 255 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(252): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3590+1622G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381531 | ||||||
| chr3:27381621
|
T | G | 1 | a0001c0004t0006g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3590+1532A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381621 | ||||||
| chr3:27381662
|
T | TA | 52 | a0001c0001t0005g0267a0001c0002t0012g0076a0001c0004t0006g0007others(49): Show | 52 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.3590+1490dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381662 | ||||||
| chr3:27381692
|
C | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.3590+1461G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381692 | ||||||
| chr3:27381784
|
T | A | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3590+1369A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381784 | ||||||
| chr3:27381873
|
G | C | 3 | a0001c0001t0014g0226a0001c0001t0014g0244a0001c0001t0014g0250 | 3 | NA18953.hp1 NA19011.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.3590+1280C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381873 | ||||||
| chr3:27381904
|
C | T | 1 | a0001c0004t0009g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3590+1249G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381904 | ||||||
| chr3:27381936
|
G | A | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.3590+1217C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381936 | ||||||
| chr3:27381976
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3590+1177G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381976 | ||||||
| chr3:27381998
|
T | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.3590+1155A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27381998 | ||||||
| chr3:27382016
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3590+1137C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382016 | ||||||
| chr3:27382058
|
A | C | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.3590+1095T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382058 | ||||||
| chr3:27382092
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3590+1061A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382092 | ||||||
| chr3:27382145
|
AGTCTTGC others(4): Show |
A | 1 | a0002c0003t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3590+997_3590+1007 others(14): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382145 | ||||||
| chr3:27382660
|
C | G | 2 | a0002c0003t0002g0186a0002c0003t0002g0187 | 2 | NA18947.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3590+493G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382660 | ||||||
| chr3:27382697
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3590+456A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382697 | ||||||
| chr3:27382924
|
T | C | 2 | a0001c0004t0006g0007a0001c0004t0006g0022 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3590+229A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27382924 | ||||||
| chr3:27383003
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3590+150A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27383003 | ||||||
| chr3:27383037
|
T | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3590+116A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27383037 | ||||||
| chr3:27383108
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3590+45A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 24/25 | chr3 | 27383108 | ||||||
| chr3:27383308
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3493-58T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27383308 | ||||||
| chr3:27383797
|
A | G | 1 | a0001c0004t0006g0015 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3493-547T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27383797 | ||||||
| chr3:27383875
|
C | A | 1 | a0003c0005t0005g0002 | 2 | NA19007.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.3493-625G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27383875 | ||||||
| chr3:27384071
|
T | C | 50 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.3493-821A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384071 | ||||||
| chr3:27384074
|
G | C | 1 | a0002c0003t0002g0187 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3493-824C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384074 | ||||||
| chr3:27384120
|
T | C | 48 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(45): Show | 48 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.3493-870A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384120 | ||||||
| chr3:27384124
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-874A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384124 | ||||||
| chr3:27384191
|
CA | C | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | HG02965.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3493-942delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384191 | ||||||
| chr3:27384217
|
G | C | 1 | a0001c0002t0011g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3493-967C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384217 | ||||||
| chr3:27384255
|
T | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3493-1005A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384255 | ||||||
| chr3:27384324
|
C | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3493-1074G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384324 | ||||||
| chr3:27384384
|
A | G | 1 | a0001c0004t0006g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3493-1134T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384384 | ||||||
| chr3:27384805
|
G | A | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.3492+1087C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27384805 | ||||||
| chr3:27385136
|
C | T | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.3492+756G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385136 | ||||||
| chr3:27385137
|
A | T | 1 | a0005c0008t0025g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3492+755T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385137 | ||||||
| chr3:27385376
|
A | G | 18 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3492+516T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385376 | ||||||
| chr3:27385444
|
T | C | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.3492+448A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385444 | ||||||
| chr3:27385464
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3492+428C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385464 | ||||||
| chr3:27385592
|
A | G | 271 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(268): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.3492+300T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385592 | ||||||
| chr3:27385734
|
A | G | 163 | a0001c0001t0001g0106a0001c0001t0001g0190a0001c0001t0001g0264others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.3492+158T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 23/25 | chr3 | 27385734 | ||||||
| chr3:27386030
|
A | G | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
splice_region_variant&intron_variant | LOW | c.3361-7T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386030 | ||||||
| chr3:27386110
|
TA | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3361-88delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386110 | ||||||
| chr3:27386125
|
A | G | 32 | a0001c0001t0002g0115a0001c0001t0003g0090a0001c0001t0003g0091others(29): Show | 32 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.3361-102T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386125 | ||||||
| chr3:27386127
|
A | G | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.3361-104T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386127 | ||||||
| chr3:27386201
|
TA | T | 78 | a0001c0001t0001g0106a0001c0001t0001g0190a0001c0001t0001g0242others(75): Show | 80 | HG00280.hp1 HG00408.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.3361-179delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386201 | ||||||
| chr3:27386201
|
TAA | T | 110 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0268others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3361-180_3361-179d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386201 | ||||||
| chr3:27386274
|
T | C | 1 | a0001c0002t0012g0076 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3361-251A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386274 | ||||||
| chr3:27386282
|
C | T | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.3361-259G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386282 | ||||||
| chr3:27386330
|
CAATT | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(78): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.3361-311_3361-308d others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386330 | ||||||
| chr3:27386725
|
C | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3361-702G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386725 | ||||||
| chr3:27386760
|
T | C | 1 | a0002c0012t0028g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3361-737A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386760 | ||||||
| chr3:27386860
|
CA | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3361-838delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386860 | ||||||
| chr3:27386880
|
G | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.3361-857C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386880 | ||||||
| chr3:27386932
|
G | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.3361-909C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386932 | ||||||
| chr3:27386991
|
A | T | 1 | a0005c0008t0025g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3361-968T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27386991 | ||||||
| chr3:27387010
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3361-987T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387010 | ||||||
| chr3:27387079
|
A | G | 3 | a0002c0003t0002g0151a0002c0003t0002g0152a0002c0003t0002g0188 | 3 | HG01070.hp2 HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3361-1056T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387079 | ||||||
| chr3:27387130
|
G | T | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(17): Show | 22 | HG00408.hp2 HG02071.hp1 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.3361-1107C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387130 | ||||||
| chr3:27387162
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3361-1139G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387162 | ||||||
| chr3:27387163
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3361-1140T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387163 | ||||||
| chr3:27387172
|
G | A | 7 | a0001c0001t0011g0052a0001c0002t0011g0048a0001c0002t0011g0053others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.3361-1149C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387172 | ||||||
| chr3:27387478
|
C | A | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3361-1455G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387478 | ||||||
| chr3:27387536
|
A | G | 1 | a0001c0002t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3361-1513T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387536 | ||||||
| chr3:27387537
|
C | T | 1 | a0002c0003t0001g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3361-1514G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387537 | ||||||
| chr3:27387565
|
C | A | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.3361-1542G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387565 | ||||||
| chr3:27387571
|
T | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3361-1548A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387571 | ||||||
| chr3:27387673
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3361-1650G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387673 | ||||||
| chr3:27387729
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3361-1706A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387729 | ||||||
| chr3:27387953
|
A | C | 3 | a0001c0001t0011g0052a0001c0002t0011g0048a0001c0002t0011g0056 | 3 | HG00140.hp1 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3361-1930T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27387953 | ||||||
| chr3:27388028
|
A | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3360+1903T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388028 | ||||||
| chr3:27388072
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG01952.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.3360+1859G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388072 | ||||||
| chr3:27388095
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3360+1836A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388095 | ||||||
| chr3:27388426
|
C | T | 1 | a0002c0003t0002g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3360+1505G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388426 | ||||||
| chr3:27388563
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3360+1368A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388563 | ||||||
| chr3:27388580
|
T | C | 1 | a0002c0003t0002g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3360+1351A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388580 | ||||||
| chr3:27388710
|
T | C | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3360+1221A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388710 | ||||||
| chr3:27388730
|
A | T | 1 | a0002c0003t0001g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3360+1201T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388730 | ||||||
| chr3:27388796
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3360+1135G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388796 | ||||||
| chr3:27388822
|
TTTC | T | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+1106_3360+110 others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388822 | ||||||
| chr3:27388832
|
A | T | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+1099T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388832 | ||||||
| chr3:27388833
|
A | ATT | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+1097_3360+109 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388833 | ||||||
| chr3:27388837
|
T | G | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+1094A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388837 | ||||||
| chr3:27388838
|
ACATAAGT others(87): Show |
A | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+999_3360+1092 others(97): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388838 | ||||||
| chr3:27388904
|
C | T | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.3360+1027G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388904 | ||||||
| chr3:27388935
|
AT | A | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+995delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388935 | ||||||
| chr3:27388940
|
AAT | A | 14 | a0001c0001t0001g0130a0001c0006t0001g0005a0001c0006t0001g0193others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+989_3360+990d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388940 | ||||||
| chr3:27388977
|
G | A | 11 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3360+954C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27388977 | ||||||
| chr3:27389100
|
T | A | 12 | a0001c0004t0006g0029a0004c0007t0001g0254a0004c0007t0008g0252others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3360+831A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27389100 | ||||||
| chr3:27389124
|
G | C | 20 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(17): Show | 20 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.3360+807C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27389124 | ||||||
| chr3:27389243
|
G | T | 18 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(15): Show | 20 | HG00408.hp2 HG02071.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.3360+688C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27389243 | ||||||
| chr3:27389602
|
A | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3360+329T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27389602 | ||||||
| chr3:27389821
|
G | C | 1 | a0001c0001t0001g0285 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3360+110C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 22/25 | chr3 | 27389821 | ||||||
| chr3:27390174
|
C | T | 1 | a0001c0001t0008g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3187-70G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390174 | ||||||
| chr3:27390304
|
A | C | 1 | a0003c0005t0005g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3187-200T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390304 | ||||||
| chr3:27390407
|
G | T | 14 | a0002c0003t0002g0151a0002c0003t0002g0152a0002c0003t0002g0158others(11): Show | 14 | HG00140.hp2 HG01070.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.3187-303C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390407 | ||||||
| chr3:27390447
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3187-343A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390447 | ||||||
| chr3:27390478
|
G | C | 12 | a0001c0004t0006g0029a0004c0007t0001g0254a0004c0007t0008g0252others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3187-374C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390478 | ||||||
| chr3:27390715
|
T | C | 164 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0297others(161): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3187-611A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390715 | ||||||
| chr3:27390808
|
G | GT | 10 | a0001c0001t0001g0136a0001c0001t0001g0281a0001c0001t0018g0035others(7): Show | 10 | HG01099.hp2 HG01361.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.3187-705dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390808 | ||||||
| chr3:27390813
|
T | C | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3187-709A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390813 | ||||||
| chr3:27390825
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3187-721A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390825 | ||||||
| chr3:27390984
|
G | A | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.3186+756C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27390984 | ||||||
| chr3:27391008
|
A | C | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3186+732T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391008 | ||||||
| chr3:27391059
|
G | A | 1 | a0001c0001t0018g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3186+681C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391059 | ||||||
| chr3:27391288
|
C | T | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.3186+452G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391288 | ||||||
| chr3:27391380
|
G | A | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.3186+360C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391380 | ||||||
| chr3:27391397
|
T | C | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.3186+343A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391397 | ||||||
| chr3:27391504
|
T | C | 68 | a0001c0001t0001g0089a0001c0001t0001g0130a0001c0001t0001g0136others(65): Show | 69 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.3186+236A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391504 | ||||||
| chr3:27391561
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3186+179C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391561 | ||||||
| chr3:27391672
|
T | C | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.3186+68A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 21/25 | chr3 | 27391672 | ||||||
| chr3:27391865
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02280.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3118-57T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27391865 | ||||||
| chr3:27391869
|
G | A | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.3118-61C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27391869 | ||||||
| chr3:27391882
|
G | A | 1 | a0002c0003t0002g0152 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3118-74C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27391882 | ||||||
| chr3:27391906
|
A | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.3118-98T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27391906 | ||||||
| chr3:27392189
|
G | A | 287 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(284): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3118-381C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392189 | ||||||
| chr3:27392420
|
T | C | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.3118-612A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392420 | ||||||
| chr3:27392541
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3118-733C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392541 | ||||||
| chr3:27392570
|
A | T | 37 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(34): Show | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.3118-762T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392570 | ||||||
| chr3:27392583
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3118-775G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392583 | ||||||
| chr3:27392643
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3118-835A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392643 | ||||||
| chr3:27392647
|
G | A | 1 | a0001c0004t0006g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3118-839C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392647 | ||||||
| chr3:27392669
|
A | G | 10 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3118-861T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392669 | ||||||
| chr3:27392770
|
G | C | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3118-962C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392770 | ||||||
| chr3:27392986
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3118-1178A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27392986 | ||||||
| chr3:27393037
|
C | T | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3118-1229G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393037 | ||||||
| chr3:27393083
|
T | C | 5 | a0001c0006t0001g0207a0001c0006t0001g0209a0001c0006t0001g0213others(2): Show | 5 | HG00639.hp2 HG01167.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.3118-1275A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393083 | ||||||
| chr3:27393241
|
A | T | 42 | a0001c0001t0001g0194a0001c0001t0001g0235a0001c0001t0001g0297others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.3117+1277T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393241 | ||||||
| chr3:27393418
|
G | C | 42 | a0001c0001t0001g0194a0001c0001t0001g0235a0001c0001t0001g0297others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.3117+1100C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393418 | ||||||
| chr3:27393449
|
G | A | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.3117+1069C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393449 | ||||||
| chr3:27393515
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3117+1003A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393515 | ||||||
| chr3:27393590
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3117+928C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393590 | ||||||
| chr3:27393793
|
G | A | 2 | a0001c0004t0006g0007a0001c0004t0006g0022 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3117+725C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393793 | ||||||
| chr3:27393911
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3117+607A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393911 | ||||||
| chr3:27393946
|
T | C | 1 | a0008c0015t0022g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3117+572A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27393946 | ||||||
| chr3:27394282
|
T | G | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.3117+236A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27394282 | ||||||
| chr3:27394363
|
C | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3117+155G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 20/25 | chr3 | 27394363 | ||||||
| chr3:27394822
|
T | G | 1 | a0004c0007t0008g0260 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2866-53A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 19/25 | chr3 | 27394822 | ||||||
| chr3:27394905
|
C | T | 1 | a0002c0003t0002g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2865+49G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 19/25 | chr3 | 27394905 | ||||||
| chr3:27395279
|
T | C | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2704-164A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395279 | ||||||
| chr3:27395285
|
T | A | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2704-170A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395285 | ||||||
| chr3:27395288
|
C | T | 1 | a0002c0003t0002g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2704-173G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395288 | ||||||
| chr3:27395306
|
T | C | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2704-191A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395306 | ||||||
| chr3:27395377
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2704-262G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395377 | ||||||
| chr3:27395380
|
T | C | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.2704-265A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395380 | ||||||
| chr3:27395395
|
C | T | 7 | a0001c0002t0004g0061a0001c0002t0004g0062a0001c0002t0004g0063others(4): Show | 7 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2704-280G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395395 | ||||||
| chr3:27395580
|
T | C | 17 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0232others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2704-465A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395580 | ||||||
| chr3:27395831
|
A | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.2704-716T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395831 | ||||||
| chr3:27395894
|
G | C | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.2704-779C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27395894 | ||||||
| chr3:27396031
|
A | T | 1 | a0001c0001t0003g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2704-916T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27396031 | ||||||
| chr3:27396386
|
T | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2704-1271A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27396386 | ||||||
| chr3:27396505
|
A | G | 52 | a0001c0001t0001g0297a0001c0001t0007g0038a0001c0001t0007g0039others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2703+1179T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27396505 | ||||||
| chr3:27396690
|
G | A | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2703+994C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27396690 | ||||||
| chr3:27396715
|
T | C | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2703+969A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27396715 | ||||||
| chr3:27396896
|
T | A | 1 | a0002c0003t0002g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2703+788A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27396896 | ||||||
| chr3:27397059
|
C | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.2703+625G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397059 | ||||||
| chr3:27397173
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2703+511C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397173 | ||||||
| chr3:27397177
|
G | A | 20 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(17): Show | 20 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2703+507C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397177 | ||||||
| chr3:27397267
|
C | T | 1 | a0001c0001t0015g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2703+417G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397267 | ||||||
| chr3:27397399
|
C | CT | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2703+284dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397399 | ||||||
| chr3:27397519
|
G | C | 1 | a0001c0006t0001g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2703+165C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397519 | ||||||
| chr3:27397674
|
T | C | 1 | a0001c0002t0004g0084 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2703+10A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 18/25 | chr3 | 27397674 | ||||||
| chr3:27397960
|
A | G | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2590-163T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 17/25 | chr3 | 27397960 | ||||||
| chr3:27398037
|
C | T | 1 | a0001c0001t0007g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2589+155G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 17/25 | chr3 | 27398037 | ||||||
| chr3:27398046
|
C | T | 2 | a0004c0007t0008g0252a0004c0007t0008g0256 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2589+146G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 17/25 | chr3 | 27398046 | ||||||
| chr3:27398058
|
C | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.2589+134G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 17/25 | chr3 | 27398058 | ||||||
| chr3:27398364
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2428-11C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398364 | ||||||
| chr3:27398397
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2428-44C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398397 | ||||||
| chr3:27398402
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2428-49G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398402 | ||||||
| chr3:27398464
|
C | G | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2428-111G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398464 | ||||||
| chr3:27398511
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2428-158G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398511 | ||||||
| chr3:27398570
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2428-217C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398570 | ||||||
| chr3:27398605
|
A | G | 24 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(21): Show | 26 | HG00408.hp2 HG00738.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.2428-252T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398605 | ||||||
| chr3:27398720
|
G | A | 2 | a0001c0001t0010g0107a0001c0001t0010g0119 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2428-367C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398720 | ||||||
| chr3:27398726
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2428-373G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27398726 | ||||||
| chr3:27399008
|
GA | G | 54 | a0001c0001t0001g0192a0001c0001t0001g0203a0001c0001t0001g0211others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2428-656delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399008 | ||||||
| chr3:27399411
|
T | C | 5 | a0001c0004t0013g0008a0001c0004t0013g0009a0001c0004t0013g0010others(2): Show | 5 | HG01243.hp2 HG01934.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2428-1058A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399411 | ||||||
| chr3:27399474
|
G | A | 1 | a0001c0002t0004g0083 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2428-1121C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399474 | ||||||
| chr3:27399501
|
C | A | 3 | a0001c0002t0004g0062a0001c0002t0004g0063a0001c0002t0004g0071 | 3 | HG02717.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2428-1148G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399501 | ||||||
| chr3:27399580
|
G | A | 1 | a0001c0006t0001g0230 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2427+1184C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399580 | ||||||
| chr3:27399648
|
T | TC | 53 | a0001c0001t0001g0243a0001c0001t0007g0038a0001c0001t0007g0039others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2427+1115dupG | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399648 | ||||||
| chr3:27399669
|
C | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2427+1095G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399669 | ||||||
| chr3:27399730
|
T | C | 20 | a0001c0001t0001g0190a0001c0001t0005g0135a0001c0001t0005g0149others(17): Show | 22 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2427+1034A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399730 | ||||||
| chr3:27399975
|
A | G | 1 | a0001c0002t0004g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2427+789T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27399975 | ||||||
| chr3:27400115
|
A | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2427+649T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27400115 | ||||||
| chr3:27400264
|
C | T | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.2427+500G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27400264 | ||||||
| chr3:27400624
|
C | G | 2 | a0001c0002t0011g0053a0001c0002t0011g0054 | 2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2427+140G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27400624 | ||||||
| chr3:27400639
|
A | G | 1 | a0001c0004t0006g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2427+125T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27400639 | ||||||
| chr3:27400665
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2427+99G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 16/25 | chr3 | 27400665 | ||||||
| chr3:27401576
|
T | C | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2322-707A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27401576 | ||||||
| chr3:27401655
|
A | G | 2 | a0001c0001t0005g0135a0001c0001t0018g0035 | 2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2322-786T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27401655 | ||||||
| chr3:27401670
|
A | G | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2322-801T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27401670 | ||||||
| chr3:27401826
|
T | C | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2322-957A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27401826 | ||||||
| chr3:27401966
|
A | G | 1 | a0001c0002t0004g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2322-1097T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27401966 | ||||||
| chr3:27401997
|
T | C | 23 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(20): Show | 23 | HG01109.hp2 HG01496.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2322-1128A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27401997 | ||||||
| chr3:27402147
|
G | A | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2321+992C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402147 | ||||||
| chr3:27402287
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2321+852G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402287 | ||||||
| chr3:27402437
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2321+702G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402437 | ||||||
| chr3:27402585
|
T | A | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2321+554A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402585 | ||||||
| chr3:27402599
|
T | C | 1 | a0001c0004t0013g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2321+540A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402599 | ||||||
| chr3:27402699
|
CA | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(218): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.2321+439delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402699 | ||||||
| chr3:27402757
|
A | AT | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2321+381dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402757 | ||||||
| chr3:27402822
|
T | C | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2321+317A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402822 | ||||||
| chr3:27402840
|
T | C | 52 | a0001c0001t0001g0297a0001c0001t0007g0038a0001c0001t0007g0039others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2321+299A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402840 | ||||||
| chr3:27402854
|
CCAAT | C | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2321+281_2321+284d others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402854 | ||||||
| chr3:27402901
|
C | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2321+238G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402901 | ||||||
| chr3:27402932
|
CAAAA | C | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2321+203_2321+206d others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27402932 | ||||||
| chr3:27403033
|
G | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2321+106C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 15/25 | chr3 | 27403033 | ||||||
| chr3:27403428
|
T | C | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2076-44A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27403428 | ||||||
| chr3:27403573
|
TTAG | T | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.2076-192_2076-190d others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27403573 | ||||||
| chr3:27403779
|
A | G | 287 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(284): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2076-395T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27403779 | ||||||
| chr3:27403893
|
T | C | 1 | a0001c0001t0003g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2076-509A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27403893 | ||||||
| chr3:27403939
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2076-555C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27403939 | ||||||
| chr3:27403968
|
C | T | 1 | a0001c0004t0009g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2076-584G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27403968 | ||||||
| chr3:27404165
|
C | T | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2075+665G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27404165 | ||||||
| chr3:27404193
|
C | T | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.2075+637G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27404193 | ||||||
| chr3:27404234
|
T | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2075+596A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27404234 | ||||||
| chr3:27404321
|
C | T | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2075+509G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27404321 | ||||||
| chr3:27404480
|
G | A | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.2075+350C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27404480 | ||||||
| chr3:27404794
|
T | A | 38 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2075+36A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 14/25 | chr3 | 27404794 | ||||||
| chr3:27405085
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1942-122G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405085 | ||||||
| chr3:27405091
|
T | G | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1942-128A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405091 | ||||||
| chr3:27405293
|
G | A | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1942-330C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405293 | ||||||
| chr3:27405744
|
T | G | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1942-781A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405744 | ||||||
| chr3:27405782
|
T | G | 1 | a0006c0011t0021g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1942-819A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405782 | ||||||
| chr3:27405832
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1942-869A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405832 | ||||||
| chr3:27405832
|
T | C | 2 | a0001c0002t0004g0082a0001c0002t0004g0083 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1942-869A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405832 | ||||||
| chr3:27405842
|
G | T | 37 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(34): Show | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1942-879C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405842 | ||||||
| chr3:27405932
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1942-969A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27405932 | ||||||
| chr3:27406006
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1942-1043C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406006 | ||||||
| chr3:27406135
|
C | T | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1942-1172G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406135 | ||||||
| chr3:27406196
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1942-1233A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406196 | ||||||
| chr3:27406234
|
C | G | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1942-1271G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406234 | ||||||
| chr3:27406258
|
T | C | 1 | a0001c0004t0006g0012 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1942-1295A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406258 | ||||||
| chr3:27406507
|
T | C | 1 | a0006c0011t0021g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1942-1544A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406507 | ||||||
| chr3:27406667
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1942-1704C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27406667 | ||||||
| chr3:27407110
|
CT | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(175): Show | 182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1942-2148delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407110 | ||||||
| chr3:27407110
|
CTT | C | 55 | a0001c0001t0001g0190a0001c0001t0003g0109a0001c0001t0003g0116others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1942-2149_1942-214 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407110 | ||||||
| chr3:27407110
|
CTTT | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1942-2150_1942-214 others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407110 | ||||||
| chr3:27407114
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1942-2151A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407114 | ||||||
| chr3:27407130
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1942-2167T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407130 | ||||||
| chr3:27407155
|
CT | C | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | HG02965.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1942-2193delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407155 | ||||||
| chr3:27407205
|
G | C | 1 | a0001c0002t0004g0085 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1941+2151C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407205 | ||||||
| chr3:27407210
|
G | A | 3 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122 | 3 | HG00280.hp1 HG01175.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1941+2146C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407210 | ||||||
| chr3:27407214
|
GCTCACGC others(7): Show |
G | 1 | a0001c0001t0003g0109 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1941+2128_1941+214 others(18): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407214 | ||||||
| chr3:27407242
|
G | A | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1941+2114C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407242 | ||||||
| chr3:27407277
|
C | T | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1941+2079G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407277 | ||||||
| chr3:27407346
|
G | C | 2 | a0002c0003t0002g0168a0002c0003t0002g0182 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1941+2010C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407346 | ||||||
| chr3:27407473
|
C | T | 1 | a0001c0001t0014g0250 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1941+1883G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407473 | ||||||
| chr3:27407478
|
CA | C | 48 | a0001c0001t0015g0087a0001c0001t0015g0088a0001c0013t0029g0251others(45): Show | 48 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1941+1877delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407478 | ||||||
| chr3:27407503
|
A | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG01952.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1941+1853T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407503 | ||||||
| chr3:27407512
|
C | T | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1941+1844G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407512 | ||||||
| chr3:27407672
|
T | C | 62 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0136others(59): Show | 64 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1941+1684A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407672 | ||||||
| chr3:27407848
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1941+1508A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407848 | ||||||
| chr3:27407911
|
C | A | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1941+1445G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407911 | ||||||
| chr3:27407936
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1941+1420G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27407936 | ||||||
| chr3:27408448
|
T | G | 53 | a0001c0001t0001g0297a0001c0001t0007g0038a0001c0001t0007g0039others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1941+908A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27408448 | ||||||
| chr3:27408457
|
A | G | 1 | a0001c0002t0004g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1941+899T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27408457 | ||||||
| chr3:27408614
|
T | C | 1 | a0010c0017t0002g0156 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1941+742A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27408614 | ||||||
| chr3:27408691
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1941+665A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27408691 | ||||||
| chr3:27408743
|
G | T | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1941+613C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 13/25 | chr3 | 27408743 | ||||||
| chr3:27409545
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1767-15A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27409545 | ||||||
| chr3:27409615
|
G | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(96): Show | 101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1767-85C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27409615 | ||||||
| chr3:27409751
|
G | T | 37 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(34): Show | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1767-221C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27409751 | ||||||
| chr3:27409961
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1767-431G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27409961 | ||||||
| chr3:27410080
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1767-550G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410080 | ||||||
| chr3:27410318
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1767-788A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410318 | ||||||
| chr3:27410443
|
A | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1767-913T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410443 | ||||||
| chr3:27410552
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1767-1022C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410552 | ||||||
| chr3:27410654
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1766+988G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410654 | ||||||
| chr3:27410756
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1766+886A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410756 | ||||||
| chr3:27410869
|
C | G | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1766+773G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410869 | ||||||
| chr3:27410912
|
T | A | 1 | a0001c0006t0001g0213 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1766+730A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410912 | ||||||
| chr3:27410949
|
G | GT | 13 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1766+692dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27410949 | ||||||
| chr3:27411025
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0245 | 2 | NA18947.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1766+617A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27411025 | ||||||
| chr3:27411204
|
T | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02280.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1766+438A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27411204 | ||||||
| chr3:27411314
|
A | G | 1 | a0002c0003t0001g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1766+328T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27411314 | ||||||
| chr3:27411453
|
A | G | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1766+189T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27411453 | ||||||
| chr3:27411521
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1766+121A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27411521 | ||||||
| chr3:27411539
|
A | C | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1766+103T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 12/25 | chr3 | 27411539 | ||||||
| chr3:27411897
|
T | A | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1660-149A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27411897 | ||||||
| chr3:27412039
|
T | C | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1660-291A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412039 | ||||||
| chr3:27412453
|
A | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1660-705T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412453 | ||||||
| chr3:27412504
|
A | G | 266 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(263): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1660-756T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412504 | ||||||
| chr3:27412606
|
A | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1660-858T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412606 | ||||||
| chr3:27412711
|
C | T | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1660-963G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412711 | ||||||
| chr3:27412726
|
TAATTA | T | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1660-983_1660-979d others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412726 | ||||||
| chr3:27412791
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1660-1043T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412791 | ||||||
| chr3:27412907
|
T | A | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1660-1159A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27412907 | ||||||
| chr3:27413005
|
C | T | 1 | a0001c0004t0006g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1660-1257G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413005 | ||||||
| chr3:27413067
|
C | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1660-1319G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413067 | ||||||
| chr3:27413473
|
A | G | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1660-1725T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413473 | ||||||
| chr3:27413771
|
A | C | 1 | a0001c0001t0001g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1660-2023T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413771 | ||||||
| chr3:27413870
|
C | T | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1660-2122G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413870 | ||||||
| chr3:27413871
|
A | T | 11 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1660-2123T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413871 | ||||||
| chr3:27413920
|
TCTTA | T | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1660-2176_1660-217 others(8): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27413920 | ||||||
| chr3:27414002
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1660-2254T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414002 | ||||||
| chr3:27414009
|
G | T | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1660-2261C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414009 | ||||||
| chr3:27414075
|
T | C | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1660-2327A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414075 | ||||||
| chr3:27414414
|
A | C | 1 | a0001c0001t0018g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1660-2666T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414414 | ||||||
| chr3:27414629
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1660-2881G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414629 | ||||||
| chr3:27414681
|
T | C | 55 | a0001c0001t0001g0297a0001c0001t0007g0038a0001c0001t0007g0039others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1660-2933A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414681 | ||||||
| chr3:27414781
|
T | C | 8 | a0001c0004t0009g0001a0001c0004t0009g0026a0001c0004t0009g0027others(5): Show | 9 | HG01884.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1660-3033A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27414781 | ||||||
| chr3:27415050
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1660-3302T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415050 | ||||||
| chr3:27415052
|
A | G | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1660-3304T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415052 | ||||||
| chr3:27415088
|
T | A | 147 | a0001c0001t0001g0106a0001c0001t0001g0297a0001c0001t0002g0115others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1660-3340A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415088 | ||||||
| chr3:27415661
|
A | G | 1 | a0001c0001t0005g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1659+2825T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415661 | ||||||
| chr3:27415667
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1659+2819A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415667 | ||||||
| chr3:27415702
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1659+2784T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415702 | ||||||
| chr3:27415708
|
C | T | 1 | a0002c0003t0001g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1659+2778G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415708 | ||||||
| chr3:27415717
|
G | A | 37 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(34): Show | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1659+2769C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415717 | ||||||
| chr3:27415741
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1659+2745C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415741 | ||||||
| chr3:27415766
|
G | C | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1659+2720C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415766 | ||||||
| chr3:27415841
|
A | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1659+2645T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415841 | ||||||
| chr3:27415857
|
A | C | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1659+2629T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415857 | ||||||
| chr3:27415969
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1659+2517A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27415969 | ||||||
| chr3:27416015
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG03704.hp1 HG03834.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1659+2471A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27416015 | ||||||
| chr3:27416209
|
G | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1659+2277C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27416209 | ||||||
| chr3:27416233
|
G | A | 1 | a0001c0001t0024g0202 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1659+2253C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27416233 | ||||||
| chr3:27416458
|
T | C | 3 | a0001c0001t0014g0226a0001c0001t0014g0244a0001c0001t0014g0250 | 3 | NA18953.hp1 NA19011.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1659+2028A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27416458 | ||||||
| chr3:27416832
|
T | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1659+1654A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27416832 | ||||||
| chr3:27416993
|
C | T | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1659+1493G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27416993 | ||||||
| chr3:27417131
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(269): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1659+1355G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27417131 | ||||||
| chr3:27417132
|
G | A | 1 | a0001c0002t0004g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1659+1354C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27417132 | ||||||
| chr3:27417423
|
A | G | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1659+1063T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27417423 | ||||||
| chr3:27417850
|
C | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1659+636G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27417850 | ||||||
| chr3:27417883
|
C | G | 18 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0149others(15): Show | 20 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1659+603G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27417883 | ||||||
| chr3:27417999
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1659+487A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27417999 | ||||||
| chr3:27418217
|
G | T | 5 | a0001c0001t0002g0115a0001c0001t0003g0116a0001c0001t0003g0117others(2): Show | 5 | HG02698.hp2 HG03490.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1659+269C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27418217 | ||||||
| chr3:27418380
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1659+106G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 11/25 | chr3 | 27418380 | ||||||
| chr3:27418741
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1513-109T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27418741 | ||||||
| chr3:27418933
|
C | T | 1 | a0001c0001t0003g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1513-301G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27418933 | ||||||
| chr3:27419296
|
C | T | 3 | a0001c0002t0004g0068a0004c0007t0001g0254a0004c0007t0008g0255 | 3 | HG02818.hp2 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1513-664G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419296 | ||||||
| chr3:27419494
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1513-862G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419494 | ||||||
| chr3:27419587
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1513-955G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419587 | ||||||
| chr3:27419628
|
G | T | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1513-996C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419628 | ||||||
| chr3:27419632
|
G | A | 11 | a0001c0002t0004g0060a0001c0002t0004g0061a0001c0002t0004g0062others(8): Show | 11 | HG02145.hp1 HG02717.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1513-1000C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419632 | ||||||
| chr3:27419806
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1512+894A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419806 | ||||||
| chr3:27419859
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1512+841C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419859 | ||||||
| chr3:27419885
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1512+815C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27419885 | ||||||
| chr3:27420015
|
C | T | 1 | a0001c0001t0003g0118 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1512+685G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27420015 | ||||||
| chr3:27420082
|
G | T | 2 | a0001c0001t0010g0107a0001c0001t0010g0119 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1512+618C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27420082 | ||||||
| chr3:27420084
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0003g0108a0001c0001t0010g0099others(7): Show | 10 | HG01891.hp1 HG02895.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1512+616C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27420084 | ||||||
| chr3:27420163
|
CA | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1512+536delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27420163 | ||||||
| chr3:27420360
|
A | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1512+340T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 10/25 | chr3 | 27420360 | ||||||
| chr3:27420949
|
C | T | 49 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1425-162G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/25 | chr3 | 27420949 | ||||||
| chr3:27420969
|
A | G | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1425-182T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/25 | chr3 | 27420969 | ||||||
| chr3:27421235
|
C | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1424+387G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/25 | chr3 | 27421235 | ||||||
| chr3:27421290
|
G | A | 2 | a0001c0001t0010g0107a0001c0001t0010g0119 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1424+332C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/25 | chr3 | 27421290 | ||||||
| chr3:27421326
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1424+296A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/25 | chr3 | 27421326 | ||||||
| chr3:27421602
|
A | G | 1 | a0001c0006t0001g0193 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1424+20T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 9/25 | chr3 | 27421602 | ||||||
| chr3:27421789
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1267-10T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27421789 | ||||||
| chr3:27421929
|
A | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1267-150T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27421929 | ||||||
| chr3:27422102
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1267-323C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422102 | ||||||
| chr3:27422208
|
A | G | 1 | a0001c0002t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1267-429T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422208 | ||||||
| chr3:27422377
|
T | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1267-598A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422377 | ||||||
| chr3:27422393
|
G | A | 1 | a0001c0002t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1267-614C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422393 | ||||||
| chr3:27422425
|
G | A | 15 | a0003c0005t0005g0002a0003c0005t0005g0003a0003c0005t0005g0133others(12): Show | 17 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1267-646C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422425 | ||||||
| chr3:27422444
|
T | C | 18 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0149others(15): Show | 20 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1267-665A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422444 | ||||||
| chr3:27422476
|
G | C | 1 | a0001c0001t0001g0291 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1267-697C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422476 | ||||||
| chr3:27422617
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1267-838T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422617 | ||||||
| chr3:27422801
|
C | T | 4 | a0001c0001t0010g0099a0001c0001t0010g0100a0001c0001t0010g0101others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267-1022G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422801 | ||||||
| chr3:27422850
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1267-1071T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27422850 | ||||||
| chr3:27423111
|
T | A | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+926A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27423111 | ||||||
| chr3:27423213
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1266+824A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27423213 | ||||||
| chr3:27423520
|
T | G | 10 | a0001c0001t0001g0106a0001c0001t0003g0108a0001c0001t0010g0099others(7): Show | 10 | HG01891.hp1 HG02895.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1266+517A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27423520 | ||||||
| chr3:27423689
|
G | A | 42 | a0001c0001t0011g0052a0001c0001t0015g0087a0001c0001t0015g0088others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1266+348C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27423689 | ||||||
| chr3:27423737
|
C | T | 3 | a0002c0003t0002g0157a0002c0003t0002g0166a0002c0003t0002g0185 | 3 | HG02040.hp1 HG02083.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1266+300G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 8/25 | chr3 | 27423737 | ||||||
| chr3:27424632
|
A | C | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1151-480T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27424632 | ||||||
| chr3:27424799
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1151-647C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27424799 | ||||||
| chr3:27424866
|
A | G | 1 | a0001c0004t0013g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1151-714T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27424866 | ||||||
| chr3:27424919
|
T | C | 1 | a0001c0002t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1151-767A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27424919 | ||||||
| chr3:27425227
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1151-1075C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425227 | ||||||
| chr3:27425305
|
G | C | 1 | a0002c0003t0002g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1151-1153C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425305 | ||||||
| chr3:27425370
|
T | TA | 13 | a0001c0001t0001g0136a0001c0001t0003g0095a0001c0001t0003g0122others(10): Show | 13 | HG01175.hp1 HG01255.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-1219dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425370 | ||||||
| chr3:27425370
|
T | TAA | 86 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0268others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1151-1220_1151-121 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425370 | ||||||
| chr3:27425370
|
T | TAAA | 28 | a0001c0001t0001g0264a0001c0001t0007g0041a0001c0001t0007g0045others(25): Show | 28 | HG00639.hp1 HG01074.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1151-1221_1151-121 others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425370 | ||||||
| chr3:27425370
|
TA | T | 62 | a0001c0001t0001g0089a0001c0001t0001g0191a0001c0001t0001g0192others(59): Show | 63 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1151-1219delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425370 | ||||||
| chr3:27425370
|
TAA | T | 7 | a0001c0001t0001g0205a0001c0001t0001g0233a0001c0001t0001g0289others(4): Show | 7 | HG00639.hp2 HG01192.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-1220_1151-121 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425370 | ||||||
| chr3:27425370
|
TAAAAAA | T | 10 | a0001c0001t0001g0106a0001c0001t0003g0108a0001c0001t0010g0099others(7): Show | 10 | HG01891.hp1 HG02895.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1151-1224_1151-121 others(10): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425370 | ||||||
| chr3:27425452
|
G | A | 1 | a0001c0001t0018g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1151-1300C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425452 | ||||||
| chr3:27425592
|
C | T | 7 | a0001c0002t0004g0061a0001c0002t0004g0062a0001c0002t0004g0063others(4): Show | 7 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-1440G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425592 | ||||||
| chr3:27425676
|
C | CA | 42 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0264others(39): Show | 42 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1151-1525dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27425676
|
C | CAA | 17 | a0001c0001t0001g0137a0001c0001t0003g0117a0001c0001t0003g0126others(14): Show | 17 | HG01243.hp1 HG01255.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.1151-1526_1151-152 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27425676
|
CA | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(78): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1151-1525delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27425676
|
CAA | C | 19 | a0001c0001t0001g0205a0001c0001t0001g0247a0001c0001t0001g0286others(16): Show | 19 | HG00323.hp1 HG01070.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1151-1526_1151-152 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27425676
|
CAAA | C | 6 | a0001c0002t0004g0061a0002c0003t0002g0176a0002c0003t0002g0183others(3): Show | 6 | HG01192.hp1 HG01346.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-1527_1151-152 others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27425676
|
CAAAA | C | 39 | a0002c0003t0001g0159a0002c0003t0002g0151a0002c0003t0002g0152others(36): Show | 39 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1151-1528_1151-152 others(8): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27425676
|
CAAAAAAA others(5): Show |
C | 1 | a0005c0008t0025g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1151-1536_1151-152 others(16): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27425676 | ||||||
| chr3:27426253
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1151-2101C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426253 | ||||||
| chr3:27426384
|
A | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1151-2232T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426384 | ||||||
| chr3:27426393
|
G | C | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1151-2241C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426393 | ||||||
| chr3:27426435
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1151-2283C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426435 | ||||||
| chr3:27426623
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1151-2471A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426623 | ||||||
| chr3:27426806
|
C | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(76): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1151-2654G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426806 | ||||||
| chr3:27426886
|
CAA | C | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1151-2736_1151-273 others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426886 | ||||||
| chr3:27426954
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1151-2802T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27426954 | ||||||
| chr3:27427059
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1151-2907T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427059 | ||||||
| chr3:27427093
|
G | A | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1151-2941C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427093 | ||||||
| chr3:27427110
|
C | A | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1151-2958G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427110 | ||||||
| chr3:27427164
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1151-3012C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427164 | ||||||
| chr3:27427317
|
CT | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(262): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1151-3166delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427317 | ||||||
| chr3:27427381
|
C | G | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1151-3229G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427381 | ||||||
| chr3:27427571
|
T | G | 1 | a0001c0001t0003g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1151-3419A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427571 | ||||||
| chr3:27427623
|
G | A | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1151-3471C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427623 | ||||||
| chr3:27427670
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1151-3518A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427670 | ||||||
| chr3:27427757
|
C | A | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1150+3541G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27427757 | ||||||
| chr3:27428043
|
T | C | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1150+3255A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27428043 | ||||||
| chr3:27428256
|
T | C | 5 | a0001c0004t0013g0008a0001c0004t0013g0009a0001c0004t0013g0010others(2): Show | 5 | HG01243.hp2 HG01934.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+3042A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27428256 | ||||||
| chr3:27428358
|
T | G | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | HG02965.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+2940A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27428358 | ||||||
| chr3:27428397
|
G | A | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1150+2901C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27428397 | ||||||
| chr3:27428564
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1150+2734A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27428564 | ||||||
| chr3:27428960
|
C | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1150+2338G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27428960 | ||||||
| chr3:27429059
|
A | G | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150+2239T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429059 | ||||||
| chr3:27429064
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150+2234C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429064 | ||||||
| chr3:27429243
|
C | T | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(20): Show | 25 | HG00408.hp2 HG01516.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.1150+2055G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429243 | ||||||
| chr3:27429326
|
T | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150+1972A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429326 | ||||||
| chr3:27429339
|
AT | A | 55 | a0001c0001t0001g0192a0001c0001t0001g0222a0001c0001t0001g0246others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1150+1958delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429339 | ||||||
| chr3:27429433
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1150+1865T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429433 | ||||||
| chr3:27429623
|
G | A | 1 | a0002c0003t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150+1675C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429623 | ||||||
| chr3:27429695
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150+1603G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429695 | ||||||
| chr3:27429708
|
G | C | 1 | a0002c0003t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150+1590C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429708 | ||||||
| chr3:27429723
|
C | T | 1 | a0003c0005t0005g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1150+1575G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429723 | ||||||
| chr3:27429868
|
C | CA | 27 | a0001c0001t0001g0291a0002c0003t0001g0162a0002c0003t0002g0151others(24): Show | 27 | HG00140.hp2 HG01070.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1150+1429dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429868 | ||||||
| chr3:27429868
|
CA | C | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+1429delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429868 | ||||||
| chr3:27429985
|
G | A | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+1313C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27429985 | ||||||
| chr3:27430128
|
G | C | 1 | a0002c0003t0002g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1150+1170C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430128 | ||||||
| chr3:27430301
|
G | GCA | 40 | a0001c0002t0011g0048a0001c0013t0029g0251a0002c0003t0001g0159others(37): Show | 40 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1150+995_1150+996d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430301 | ||||||
| chr3:27430340
|
A | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1150+958T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430340 | ||||||
| chr3:27430344
|
C | T | 1 | a0001c0004t0006g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1150+954G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430344 | ||||||
| chr3:27430467
|
G | A | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1150+831C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430467 | ||||||
| chr3:27430491
|
C | T | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1150+807G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430491 | ||||||
| chr3:27430569
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1150+729C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430569 | ||||||
| chr3:27430605
|
C | CA | 111 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0136others(108): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1150+692dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430605 | ||||||
| chr3:27430605
|
C | CAA | 7 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0018g0035others(4): Show | 7 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150+691_1150+692d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430605 | ||||||
| chr3:27430655
|
C | T | 1 | a0009c0014t0001g0248 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1150+643G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430655 | ||||||
| chr3:27430809
|
G | C | 3 | a0001c0004t0013g0008a0001c0004t0013g0009a0001c0004t0013g0010 | 3 | HG01243.hp2 HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1150+489C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430809 | ||||||
| chr3:27430873
|
C | T | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150+425G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430873 | ||||||
| chr3:27430924
|
T | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1150+374A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27430924 | ||||||
| chr3:27431276
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1150+22T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 7/25 | chr3 | 27431276 | ||||||
| chr3:27431707
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.779-38T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27431707 | ||||||
| chr3:27431753
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.779-84A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27431753 | ||||||
| chr3:27431842
|
A | G | 4 | a0001c0001t0003g0092a0001c0001t0003g0109a0001c0001t0003g0110others(1): Show | 4 | HG00673.hp1 NA18977.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-173T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27431842 | ||||||
| chr3:27431950
|
G | C | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.779-281C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27431950 | ||||||
| chr3:27432065
|
G | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(76): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.779-396C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27432065 | ||||||
| chr3:27432190
|
A | G | 1 | a0008c0015t0022g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.779-521T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27432190 | ||||||
| chr3:27432641
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.779-972C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27432641 | ||||||
| chr3:27432827
|
G | T | 3 | a0001c0002t0004g0077a0001c0002t0004g0078a0001c0002t0004g0080 | 3 | NA18943.hp1 NA18963.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.778+1089C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27432827 | ||||||
| chr3:27432904
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.778+1012A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27432904 | ||||||
| chr3:27433024
|
T | G | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.778+892A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433024 | ||||||
| chr3:27433134
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.778+782T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433134 | ||||||
| chr3:27433135
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.778+781T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433135 | ||||||
| chr3:27433136
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.778+780T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433136 | ||||||
| chr3:27433722
|
A | G | 11 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.778+194T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433722 | ||||||
| chr3:27433823
|
G | A | 4 | a0001c0001t0007g0039a0001c0001t0007g0040a0001c0001t0007g0041others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+93C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433823 | ||||||
| chr3:27433860
|
G | A | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.778+56C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433860 | ||||||
| chr3:27433894
|
T | A | 11 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.778+22A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 6/25 | chr3 | 27433894 | ||||||
| chr3:27434231
|
CAAAT | C | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.590-131_590-128del others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27434231 | ||||||
| chr3:27434452
|
C | T | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.590-348G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27434452 | ||||||
| chr3:27434718
|
A | T | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.590-614T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27434718 | ||||||
| chr3:27434843
|
C | G | 11 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.590-739G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27434843 | ||||||
| chr3:27434863
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.590-759C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27434863 | ||||||
| chr3:27435043
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.590-939C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27435043 | ||||||
| chr3:27435282
|
T | G | 1 | a0001c0004t0006g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.589+1106A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27435282 | ||||||
| chr3:27435733
|
T | G | 1 | a0006c0011t0021g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.589+655A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27435733 | ||||||
| chr3:27435798
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.589+590C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27435798 | ||||||
| chr3:27435846
|
C | T | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.589+542G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27435846 | ||||||
| chr3:27435995
|
A | C | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.589+393T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27435995 | ||||||
| chr3:27436133
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.589+255T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27436133 | ||||||
| chr3:27436223
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0293 | 2 | NA18942.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.589+165A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 5/25 | chr3 | 27436223 | ||||||
| chr3:27436555
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG02074.hp1 HG02683.hp2 NA18942.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.429-7C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27436555 | ||||||
| chr3:27436638
|
G | GA | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.429-91dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27436638 | ||||||
| chr3:27436876
|
C | T | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.429-328G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27436876 | ||||||
| chr3:27437078
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.428+310G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27437078 | ||||||
| chr3:27437149
|
G | A | 1 | a0001c0004t0006g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.428+239C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27437149 | ||||||
| chr3:27437219
|
C | T | 49 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.428+169G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27437219 | ||||||
| chr3:27437306
|
G | A | 43 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(40): Show | 43 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.428+82C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27437306 | ||||||
| chr3:27437343
|
C | T | 53 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.428+45G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 4/25 | chr3 | 27437343 | ||||||
| chr3:27437549
|
T | C | 2 | a0001c0001t0007g0042a0001c0001t0007g0047 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.290-23A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27437549 | ||||||
| chr3:27437989
|
G | A | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.290-463C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27437989 | ||||||
| chr3:27438026
|
G | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.290-500C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438026 | ||||||
| chr3:27438070
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0281 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.290-544C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438070 | ||||||
| chr3:27438101
|
G | A | 43 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(40): Show | 43 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.290-575C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438101 | ||||||
| chr3:27438111
|
C | T | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.290-585G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438111 | ||||||
| chr3:27438420
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.290-894C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438420 | ||||||
| chr3:27438468
|
C | G | 146 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.290-942G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438468 | ||||||
| chr3:27438555
|
C | A | 1 | a0001c0004t0006g0011 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.290-1029G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438555 | ||||||
| chr3:27438556
|
A | G | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.290-1030T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438556 | ||||||
| chr3:27438593
|
AATAAC | A | 42 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(39): Show | 42 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.290-1072_290-1068d others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438593 | ||||||
| chr3:27438598
|
CATAACAT others(3): Show |
C | 2 | a0001c0001t0010g0099a0001c0001t0010g0100 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.290-1082_290-1073d others(12): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438598 | ||||||
| chr3:27438615
|
TAACAAAA others(23): Show |
T | 1 | a0001c0006t0001g0193 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.290-1119_290-1090d others(32): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438615 | ||||||
| chr3:27438672
|
T | TAAC | 147 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.290-1147_290-1146i others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438672 | ||||||
| chr3:27438934
|
G | T | 1 | a0002c0003t0002g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.290-1408C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438934 | ||||||
| chr3:27438936
|
G | A | 1 | a0004c0007t0008g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.290-1410C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27438936 | ||||||
| chr3:27439050
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-1524G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439050 | ||||||
| chr3:27439276
|
G | A | 1 | a0001c0004t0006g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.290-1750C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439276 | ||||||
| chr3:27439417
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.290-1891A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439417 | ||||||
| chr3:27439506
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-1980C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439506 | ||||||
| chr3:27439550
|
A | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(87): Show | 92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.290-2024T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439550 | ||||||
| chr3:27439560
|
T | C | 4 | a0001c0001t0010g0099a0001c0001t0010g0100a0001c0001t0010g0101others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2034A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439560 | ||||||
| chr3:27439620
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.290-2094A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439620 | ||||||
| chr3:27439752
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-2226G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439752 | ||||||
| chr3:27439780
|
A | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-2254T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439780 | ||||||
| chr3:27439870
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-2344A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27439870 | ||||||
| chr3:27440119
|
T | C | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.290-2593A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440119 | ||||||
| chr3:27440355
|
G | A | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.290-2829C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440355 | ||||||
| chr3:27440484
|
T | G | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.290-2958A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440484 | ||||||
| chr3:27440500
|
G | A | 1 | a0005c0008t0025g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.290-2974C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440500 | ||||||
| chr3:27440547
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.290-3021C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440547 | ||||||
| chr3:27440557
|
G | A | 1 | a0002c0003t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290-3031C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440557 | ||||||
| chr3:27440689
|
C | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.290-3163G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440689 | ||||||
| chr3:27440722
|
C | T | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.290-3196G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440722 | ||||||
| chr3:27440879
|
T | C | 1 | a0008c0015t0022g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.290-3353A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440879 | ||||||
| chr3:27440970
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.290-3444T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27440970 | ||||||
| chr3:27441012
|
A | T | 147 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.290-3486T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441012 | ||||||
| chr3:27441045
|
C | CA | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-3520dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441045 | ||||||
| chr3:27441201
|
C | T | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.290-3675G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441201 | ||||||
| chr3:27441330
|
T | G | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.290-3804A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441330 | ||||||
| chr3:27441387
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.290-3861A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441387 | ||||||
| chr3:27441445
|
T | C | 4 | a0002c0003t0002g0177a0002c0003t0002g0178a0002c0003t0002g0179others(1): Show | 4 | HG00738.hp1 HG01074.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-3919A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441445 | ||||||
| chr3:27441561
|
T | C | 3 | a0001c0006t0001g0005a0001c0006t0001g0223a0003c0005t0005g0139 | 4 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-4035A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441561 | ||||||
| chr3:27441563
|
G | T | 1 | a0002c0003t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290-4037C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441563 | ||||||
| chr3:27441673
|
T | C | 100 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(97): Show | 102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.290-4147A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441673 | ||||||
| chr3:27441769
|
C | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.290-4243G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441769 | ||||||
| chr3:27441890
|
A | G | 1 | a0003c0005t0005g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.290-4364T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441890 | ||||||
| chr3:27441900
|
CTT | C | 10 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-4376_290-4375d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27441900 | ||||||
| chr3:27442194
|
A | G | 1 | a0002c0003t0002g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.290-4668T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442194 | ||||||
| chr3:27442407
|
A | G | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.290-4881T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442407 | ||||||
| chr3:27442414
|
G | A | 1 | a0001c0002t0004g0085 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.290-4888C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442414 | ||||||
| chr3:27442418
|
C | T | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.290-4892G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442418 | ||||||
| chr3:27442441
|
CT | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(160): Show | 165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.290-4916delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442441 | ||||||
| chr3:27442503
|
G | A | 1 | a0001c0004t0013g0023 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.290-4977C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442503 | ||||||
| chr3:27442734
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.290-5208C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442734 | ||||||
| chr3:27442850
|
G | C | 1 | a0001c0002t0004g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-5324C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442850 | ||||||
| chr3:27442909
|
T | C | 1 | a0001c0001t0005g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.290-5383A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442909 | ||||||
| chr3:27442935
|
T | G | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.290-5409A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27442935 | ||||||
| chr3:27443024
|
C | CT | 57 | a0001c0001t0001g0137a0001c0001t0001g0264a0001c0001t0001g0265others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.290-5499dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443024 | ||||||
| chr3:27443024
|
C | CTT | 7 | a0001c0001t0001g0269a0001c0001t0001g0284a0001c0002t0004g0073others(4): Show | 7 | HG02145.hp1 HG03098.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-5500_290-5499d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443024 | ||||||
| chr3:27443024
|
C | CTTT | 15 | a0001c0001t0005g0135a0001c0001t0018g0035a0003c0005t0005g0002others(12): Show | 17 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.290-5501_290-5499d others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443024 | ||||||
| chr3:27443024
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.290-5511_290-5499d others(15): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443024 | ||||||
| chr3:27443031
|
TC | T | 45 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0204others(42): Show | 45 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.290-5506delG | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443031 | ||||||
| chr3:27443032
|
C | T | 171 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(168): Show | 175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.290-5506G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443032 | ||||||
| chr3:27443112
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.289+5539T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443112 | ||||||
| chr3:27443162
|
C | G | 1 | a0001c0004t0013g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.289+5489G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443162 | ||||||
| chr3:27443219
|
G | A | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.289+5432C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443219 | ||||||
| chr3:27443354
|
C | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.289+5297G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443354 | ||||||
| chr3:27443365
|
T | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.289+5286A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443365 | ||||||
| chr3:27443389
|
T | C | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.289+5262A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443389 | ||||||
| chr3:27443458
|
G | A | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.289+5193C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443458 | ||||||
| chr3:27443563
|
C | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.289+5088G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443563 | ||||||
| chr3:27443740
|
A | G | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.289+4911T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443740 | ||||||
| chr3:27443989
|
G | C | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.289+4662C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27443989 | ||||||
| chr3:27444036
|
C | G | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.289+4615G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444036 | ||||||
| chr3:27444094
|
C | T | 18 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0018g0035others(15): Show | 20 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.289+4557G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444094 | ||||||
| chr3:27444096
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.289+4555T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444096 | ||||||
| chr3:27444124
|
C | T | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.289+4527G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444124 | ||||||
| chr3:27444227
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.289+4424C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444227 | ||||||
| chr3:27444239
|
C | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(97): Show | 102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.289+4412G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444239 | ||||||
| chr3:27444526
|
A | C | 1 | a0001c0001t0020g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.289+4125T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444526 | ||||||
| chr3:27444553
|
G | T | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.289+4098C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444553 | ||||||
| chr3:27444574
|
C | T | 12 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(9): Show | 14 | HG02074.hp2 HG02258.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.289+4077G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444574 | ||||||
| chr3:27444884
|
G | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+3767C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27444884 | ||||||
| chr3:27445089
|
T | C | 1 | a0002c0003t0001g0159 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.289+3562A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445089 | ||||||
| chr3:27445389
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.289+3262C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445389 | ||||||
| chr3:27445620
|
TTAA | T | 16 | a0001c0001t0005g0149a0003c0005t0005g0002a0003c0005t0005g0003others(13): Show | 18 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.289+3028_289+3030d others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445620 | ||||||
| chr3:27445627
|
T | C | 1 | a0001c0001t0015g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.289+3024A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445627 | ||||||
| chr3:27445682
|
C | T | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.289+2969G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445682 | ||||||
| chr3:27445736
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.289+2915T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445736 | ||||||
| chr3:27445763
|
C | CA | 34 | a0001c0004t0013g0009a0002c0003t0001g0162a0002c0003t0002g0151others(31): Show | 34 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.289+2887dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445763 | ||||||
| chr3:27445763
|
CA | C | 209 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(206): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.289+2887delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445763 | ||||||
| chr3:27445782
|
A | C | 1 | a0001c0001t0015g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.289+2869T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445782 | ||||||
| chr3:27445823
|
T | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0245 | 2 | NA18947.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.289+2828A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445823 | ||||||
| chr3:27445931
|
C | CA | 9 | a0001c0004t0006g0012a0001c0004t0006g0017a0001c0004t0006g0020others(6): Show | 10 | HG00642.hp2 HG01106.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+2719dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445931 | ||||||
| chr3:27445931
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0108 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.289+2706_289+2719d others(16): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445931 | ||||||
| chr3:27445931
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0002g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.289+2705_289+2719d others(17): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445931 | ||||||
| chr3:27445948
|
AAAAAAAA others(12): Show |
A | 3 | a0002c0003t0002g0164a0005c0008t0002g0153a0010c0017t0002g0156 | 3 | HG03041.hp1 HG03834.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.289+2684_289+2702d others(21): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445948 | ||||||
| chr3:27445949
|
AAAAAAAA others(9): Show |
A | 5 | a0002c0003t0002g0169a0002c0003t0002g0170a0002c0003t0002g0176others(2): Show | 5 | HG01192.hp1 HG01255.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+2686_289+2701d others(18): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445949 | ||||||
| chr3:27445949
|
AAAAAAAA others(11): Show |
A | 25 | a0002c0003t0001g0159a0002c0003t0002g0151a0002c0003t0002g0152others(22): Show | 25 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.289+2684_289+2701d others(20): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445949 | ||||||
| chr3:27445950
|
AAAAAAAA others(10): Show |
A | 1 | a0002c0003t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.289+2684_289+2700d others(19): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445950 | ||||||
| chr3:27445950
|
AAAAAAAA others(12): Show |
A | 1 | a0002c0003t0002g0172 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.289+2682_289+2700d others(21): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445950 | ||||||
| chr3:27445951
|
AAAAAAAA others(11): Show |
A | 2 | a0002c0003t0002g0168a0002c0003t0002g0182 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.289+2682_289+2699d others(20): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445951 | ||||||
| chr3:27445951
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.289+2678_289+2699d others(24): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445951 | ||||||
| chr3:27445957
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0002t0011g0053 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.289+2678_289+2693d others(18): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445957 | ||||||
| chr3:27445958
|
AAAAAAAT others(6): Show |
A | 20 | a0001c0001t0005g0149a0001c0002t0004g0061a0001c0002t0004g0062others(17): Show | 22 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.289+2680_289+2692d others(15): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445958 | ||||||
| chr3:27445958
|
AAAAAAAT others(8): Show |
A | 20 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0065others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.289+2678_289+2692d others(17): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445958 | ||||||
| chr3:27445959
|
AAAAAATA others(3): Show |
A | 2 | a0001c0001t0001g0277a0001c0001t0005g0267 | 2 | HG01496.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.289+2682_289+2691d others(12): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445959 | ||||||
| chr3:27445959
|
AAAAAATA others(5): Show |
A | 21 | a0001c0001t0001g0195a0001c0001t0001g0264a0001c0001t0001g0265others(18): Show | 21 | HG01109.hp2 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.289+2680_289+2691d others(14): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445959 | ||||||
| chr3:27445959
|
AAAAAATA others(7): Show |
A | 14 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.289+2678_289+2691d others(16): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445959 | ||||||
| chr3:27445960
|
AAAAATAT others(4): Show |
A | 1 | a0001c0002t0004g0080 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.289+2680_289+2690d others(13): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445960 | ||||||
| chr3:27445960
|
AAAAATAT others(6): Show |
A | 15 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(12): Show | 15 | HG00323.hp2 HG01361.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+2678_289+2690d others(15): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445960 | ||||||
| chr3:27445960
|
AAAAATAT others(8): Show |
A | 6 | a0001c0001t0020g0036a0001c0002t0004g0068a0001c0002t0004g0082others(3): Show | 6 | HG02572.hp2 HG02965.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+2676_289+2690d others(17): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445960 | ||||||
| chr3:27445961
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0001g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.289+2680_289+2689d others(12): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445961 | ||||||
| chr3:27445961
|
AAAATATA others(5): Show |
A | 56 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(53): Show | 58 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.289+2678_289+2689d others(14): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445961 | ||||||
| chr3:27445962
|
AAATATAT others(4): Show |
A | 17 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0194others(14): Show | 17 | HG00280.hp2 HG01167.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.289+2678_289+2688d others(13): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445962 | ||||||
| chr3:27445962
|
AAATATAT others(6): Show |
A | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.289+2676_289+2688d others(15): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445962 | ||||||
| chr3:27445963
|
A | AAAATAT | 8 | a0001c0001t0003g0091a0001c0001t0003g0092a0001c0001t0003g0110others(5): Show | 8 | HG00741.hp2 HG01255.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+2687_289+2688i others(8): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445963 | ||||||
| chr3:27445963
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0003g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.289+2687_289+2688i others(16): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445963 | ||||||
| chr3:27445963
|
A | AAATAT | 9 | a0001c0001t0003g0090a0001c0001t0003g0096a0001c0001t0003g0109others(6): Show | 9 | HG00673.hp1 HG01257.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.289+2687_289+2688i others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445963 | ||||||
| chr3:27445963
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0030g0114 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.289+2687_289+2688i others(13): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445963 | ||||||
| chr3:27445963
|
A | T | 3 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0004t0009g0033 | 3 | HG00280.hp1 HG03195.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.289+2688T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445963 | ||||||
| chr3:27445963
|
AATATATA others(3): Show |
A | 4 | a0001c0001t0001g0196a0001c0001t0001g0200a0001c0001t0001g0287others(1): Show | 4 | HG02602.hp2 HG03942.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+2678_289+2687d others(12): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445963 | ||||||
| chr3:27445965
|
T | A | 6 | a0001c0001t0001g0106a0001c0001t0010g0105a0001c0001t0010g0113others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+2686A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445965 | ||||||
| chr3:27445967
|
T | A | 3 | a0001c0004t0013g0008a0001c0004t0013g0009a0001c0004t0013g0010 | 3 | HG01243.hp2 HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.289+2684A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445967 | ||||||
| chr3:27445969
|
T | A | 1 | a0001c0004t0013g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.289+2682A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445969 | ||||||
| chr3:27445975
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.289+2676A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27445975 | ||||||
| chr3:27446118
|
G | GTA | 149 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(146): Show | 151 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.289+2532_289+2533i others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446118 | ||||||
| chr3:27446122
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0003g0199 | 2 | HG04115.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.289+2529C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446122 | ||||||
| chr3:27446124
|
G | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(76): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.289+2527C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446124 | ||||||
| chr3:27446126
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0003g0199 | 2 | HG04115.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.289+2525C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446126 | ||||||
| chr3:27446131
|
T | C | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.289+2520A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446131 | ||||||
| chr3:27446141
|
A | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(78): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.289+2510T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446141 | ||||||
| chr3:27446214
|
C | T | 144 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.289+2437G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446214 | ||||||
| chr3:27446281
|
G | A | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.289+2370C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446281 | ||||||
| chr3:27446425
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(78): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.289+2226A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446425 | ||||||
| chr3:27446618
|
A | G | 16 | a0001c0001t0005g0149a0003c0005t0005g0002a0003c0005t0005g0003others(13): Show | 18 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.289+2033T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446618 | ||||||
| chr3:27446791
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.289+1860A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446791 | ||||||
| chr3:27446819
|
T | G | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.289+1832A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446819 | ||||||
| chr3:27446866
|
TTTTTTTT others(2): Show |
T | 19 | a0002c0003t0002g0157a0002c0003t0002g0158a0002c0003t0002g0164others(16): Show | 19 | HG00140.hp2 HG01346.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.289+1776_289+1784d others(11): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446866 | ||||||
| chr3:27446867
|
TTTTTTTT others(1): Show |
T | 10 | a0002c0003t0001g0162a0002c0003t0002g0161a0002c0003t0002g0163others(7): Show | 10 | HG00738.hp1 HG01074.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+1776_289+1783d others(10): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446867 | ||||||
| chr3:27446868
|
TTTTTTTG | T | 12 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0002g0160others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1776_289+1782d others(9): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446868 | ||||||
| chr3:27446873
|
TTGTTTTT others(5): Show |
T | 34 | a0001c0001t0002g0115a0001c0001t0003g0090a0001c0001t0003g0092others(31): Show | 34 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.289+1766_289+1777d others(14): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446873 | ||||||
| chr3:27446874
|
TGTTTTTT others(4): Show |
T | 8 | a0001c0001t0001g0106a0001c0001t0003g0091a0001c0001t0003g0095others(5): Show | 8 | HG00741.hp2 HG01175.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+1766_289+1776d others(13): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446874 | ||||||
| chr3:27446875
|
G | GT | 6 | a0001c0001t0001g0190a0001c0001t0001g0211a0001c0001t0001g0227others(3): Show | 6 | HG00639.hp2 HG01175.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+1775dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446875 | ||||||
| chr3:27446875
|
G | T | 3 | a0002c0003t0002g0151a0002c0003t0002g0152a0002c0003t0002g0188 | 3 | HG01070.hp2 HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.289+1776C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446875 | ||||||
| chr3:27446882
|
TTTGTTTT others(5): Show |
T | 15 | a0003c0005t0005g0002a0003c0005t0005g0003a0003c0005t0005g0133others(12): Show | 17 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.289+1757_289+1768d others(14): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446882 | ||||||
| chr3:27446884
|
TGTTTTTT others(3): Show |
T | 3 | a0002c0003t0002g0151a0002c0003t0002g0152a0002c0003t0002g0188 | 3 | HG01070.hp2 HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.289+1757_289+1766d others(12): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446884 | ||||||
| chr3:27446885
|
G | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(139): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.289+1766C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446885 | ||||||
| chr3:27446885
|
GTTTTTTT others(4): Show |
G | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.289+1755_289+1765d others(13): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446885 | ||||||
| chr3:27446886
|
T | G | 92 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(89): Show | 94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.289+1765A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446886 | ||||||
| chr3:27446886
|
T | TG | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01109.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.289+1764_289+1765i others(3): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446886 | ||||||
| chr3:27446891
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.289+1760A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446891 | ||||||
| chr3:27446893
|
TG | T | 4 | a0001c0001t0002g0263a0001c0001t0015g0087a0001c0001t0015g0088others(1): Show | 4 | HG01516.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+1757delC | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446893 | ||||||
| chr3:27446894
|
G | T | 231 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(228): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.289+1757C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446894 | ||||||
| chr3:27446896
|
T | G | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.289+1755A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27446896 | ||||||
| chr3:27447165
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0002g0263 | 2 | HG02630.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.289+1486G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447165 | ||||||
| chr3:27447166
|
G | A | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.289+1485C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447166 | ||||||
| chr3:27447320
|
A | T | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.289+1331T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447320 | ||||||
| chr3:27447339
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.289+1312A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447339 | ||||||
| chr3:27447485
|
T | C | 1 | a0001c0002t0011g0053 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.289+1166A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447485 | ||||||
| chr3:27447513
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.289+1138A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447513 | ||||||
| chr3:27447611
|
C | T | 272 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(269): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.289+1040G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447611 | ||||||
| chr3:27447640
|
C | CT | 64 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0137others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.289+1010dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447640 | ||||||
| chr3:27447640
|
C | CTT | 47 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(44): Show | 48 | HG00642.hp1 HG00673.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.289+1009_289+1010d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447640 | ||||||
| chr3:27447640
|
C | CTTT | 9 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0111others(6): Show | 9 | HG00280.hp1 HG00735.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+1008_289+1010d others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447640 | ||||||
| chr3:27447640
|
CTTTTTTT others(4): Show |
C | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.289+1000_289+1010d others(13): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447640 | ||||||
| chr3:27447673
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.289+978G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447673 | ||||||
| chr3:27447736
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.289+915C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447736 | ||||||
| chr3:27447812
|
C | T | 1 | a0002c0003t0002g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.289+839G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447812 | ||||||
| chr3:27447980
|
G | A | 1 | a0001c0006t0001g0225 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.289+671C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27447980 | ||||||
| chr3:27448084
|
C | T | 1 | a0002c0003t0002g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.289+567G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448084 | ||||||
| chr3:27448134
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.289+517G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448134 | ||||||
| chr3:27448147
|
C | T | 12 | a0001c0001t0018g0035a0004c0007t0001g0254a0004c0007t0008g0252others(9): Show | 12 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+504G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448147 | ||||||
| chr3:27448155
|
T | C | 1 | a0001c0001t0003g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.289+496A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448155 | ||||||
| chr3:27448216
|
C | CA | 51 | a0001c0001t0001g0106a0001c0001t0001g0197a0001c0001t0001g0200others(48): Show | 51 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.289+434dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448216 | ||||||
| chr3:27448216
|
C | CAA | 43 | a0001c0001t0001g0130a0001c0001t0002g0115a0001c0001t0003g0090others(40): Show | 43 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.289+433_289+434dup others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448216 | ||||||
| chr3:27448216
|
CA | C | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.289+434delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448216 | ||||||
| chr3:27448263
|
C | T | 4 | a0001c0001t0001g0106a0001c0001t0003g0108a0001c0001t0010g0105others(1): Show | 4 | NA18959.hp2 NA18963.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+388G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448263 | ||||||
| chr3:27448333
|
T | C | 10 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+318A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448333 | ||||||
| chr3:27448382
|
T | C | 1 | a0001c0004t0006g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.289+269A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448382 | ||||||
| chr3:27448402
|
G | C | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.289+249C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448402 | ||||||
| chr3:27448434
|
C | G | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.289+217G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448434 | ||||||
| chr3:27448505
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.289+146T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448505 | ||||||
| chr3:27448616
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.289+35G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 3/25 | chr3 | 27448616 | ||||||
| chr3:27449009
|
A | G | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0277others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-212T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449009 | ||||||
| chr3:27449043
|
A | T | 1 | a0001c0001t0001g0235 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.143-246T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449043 | ||||||
| chr3:27449047
|
C | CT | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.143-251dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449047 | ||||||
| chr3:27449136
|
C | G | 272 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(269): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.143-339G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449136 | ||||||
| chr3:27449193
|
C | A | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.143-396G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449193 | ||||||
| chr3:27449257
|
A | G | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.143-460T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449257 | ||||||
| chr3:27449363
|
TAAC | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-569_143-567del others(3): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449363 | ||||||
| chr3:27449564
|
A | G | 1 | a0001c0004t0016g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.143-767T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27449564 | ||||||
| chr3:27450008
|
A | T | 1 | a0001c0002t0004g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.143-1211T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450008 | ||||||
| chr3:27450071
|
C | G | 1 | a0001c0004t0016g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.143-1274G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450071 | ||||||
| chr3:27450536
|
G | C | 1 | a0001c0001t0001g0243 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.143-1739C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450536 | ||||||
| chr3:27450563
|
A | T | 1 | a0001c0001t0001g0286 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.143-1766T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450563 | ||||||
| chr3:27450612
|
G | A | 1 | a0001c0001t0018g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142+1805C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450612 | ||||||
| chr3:27450619
|
T | C | 10 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142+1798A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450619 | ||||||
| chr3:27450659
|
G | C | 101 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(98): Show | 103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.142+1758C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450659 | ||||||
| chr3:27450660
|
A | G | 3 | a0002c0003t0002g0151a0002c0003t0002g0152a0002c0003t0002g0188 | 3 | HG01070.hp2 HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.142+1757T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450660 | ||||||
| chr3:27450696
|
A | G | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.142+1721T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450696 | ||||||
| chr3:27450800
|
G | A | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | HG02965.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+1617C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450800 | ||||||
| chr3:27450940
|
A | G | 1 | a0001c0002t0011g0048 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.142+1477T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450940 | ||||||
| chr3:27450943
|
T | C | 1 | a0001c0006t0001g0230 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.142+1474A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27450943 | ||||||
| chr3:27451109
|
A | T | 3 | a0002c0003t0002g0169a0002c0003t0002g0176a0002c0003t0027g0184 | 3 | HG01192.hp1 HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.142+1308T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451109 | ||||||
| chr3:27451140
|
T | TA | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.142+1276dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451140 | ||||||
| chr3:27451177
|
T | C | 3 | a0001c0001t0015g0087a0001c0001t0015g0088a0001c0002t0011g0048 | 3 | HG01516.hp2 HG03017.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.142+1240A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451177 | ||||||
| chr3:27451495
|
C | A | 1 | a0008c0015t0022g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.142+922G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451495 | ||||||
| chr3:27451723
|
A | C | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.142+694T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451723 | ||||||
| chr3:27451837
|
T | A | 1 | a0002c0003t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142+580A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451837 | ||||||
| chr3:27451885
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.142+532A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27451885 | ||||||
| chr3:27452060
|
T | C | 1 | a0001c0004t0009g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142+357A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27452060 | ||||||
| chr3:27452145
|
G | A | 1 | a0001c0004t0006g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.142+272C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 2/25 | chr3 | 27452145 | ||||||
| chr3:27452805
|
G | A | 1 | a0002c0003t0002g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.61-307C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27452805 | ||||||
| chr3:27452932
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.61-434T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27452932 | ||||||
| chr3:27452975
|
T | C | 1 | a0001c0001t0003g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.61-477A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27452975 | ||||||
| chr3:27452984
|
T | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-486A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27452984 | ||||||
| chr3:27453030
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-532T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453030 | ||||||
| chr3:27453098
|
A | C | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-600T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453098 | ||||||
| chr3:27453129
|
A | T | 101 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(98): Show | 103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.61-631T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453129 | ||||||
| chr3:27453212
|
G | A | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.61-714C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453212 | ||||||
| chr3:27453284
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.61-786A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453284 | ||||||
| chr3:27453440
|
C | A | 1 | a0001c0004t0006g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.61-942G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453440 | ||||||
| chr3:27453482
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-984T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453482 | ||||||
| chr3:27453483
|
C | T | 1 | a0001c0004t0006g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.61-985G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453483 | ||||||
| chr3:27453484
|
G | A | 1 | a0001c0001t0015g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-986C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453484 | ||||||
| chr3:27453528
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-1030T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453528 | ||||||
| chr3:27453622
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-1124A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453622 | ||||||
| chr3:27453655
|
A | T | 1 | a0001c0004t0006g0015 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.61-1157T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453655 | ||||||
| chr3:27453990
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.61-1492T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27453990 | ||||||
| chr3:27454082
|
G | A | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-1584C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27454082 | ||||||
| chr3:27454095
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-1597T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27454095 | ||||||
| chr3:27454983
|
C | T | 1 | a0010c0017t0002g0156 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.61-2485G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27454983 | ||||||
| chr3:27454995
|
C | A | 2 | a0002c0012t0028g0154a0005c0008t0025g0155 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.61-2497G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27454995 | ||||||
| chr3:27455010
|
T | TA | 52 | a0001c0001t0003g0093a0001c0001t0003g0094a0001c0013t0029g0251others(49): Show | 52 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.61-2513dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455010 | ||||||
| chr3:27455024
|
G | A | 1 | a0002c0003t0002g0185 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.61-2526C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455024 | ||||||
| chr3:27455041
|
G | A | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.61-2543C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455041 | ||||||
| chr3:27455061
|
C | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-2563G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455061 | ||||||
| chr3:27455536
|
T | C | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-3038A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455536 | ||||||
| chr3:27455570
|
A | AT | 105 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(102): Show | 107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.61-3073dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455570 | ||||||
| chr3:27455570
|
A | ATTT | 8 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0255others(5): Show | 8 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-3075_61-3073dup others(3): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455570 | ||||||
| chr3:27455592
|
G | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-3094C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455592 | ||||||
| chr3:27455613
|
G | A | 3 | a0001c0001t0014g0226a0001c0001t0014g0244a0001c0001t0014g0250 | 3 | NA18953.hp1 NA19011.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.61-3115C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455613 | ||||||
| chr3:27455659
|
C | T | 1 | a0001c0006t0001g0193 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.61-3161G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455659 | ||||||
| chr3:27455670
|
G | A | 1 | a0008c0015t0022g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.61-3172C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455670 | ||||||
| chr3:27455704
|
C | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-3206G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455704 | ||||||
| chr3:27455819
|
C | T | 91 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.61-3321G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27455819 | ||||||
| chr3:27456036
|
G | A | 1 | a0001c0004t0013g0023 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.61-3538C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456036 | ||||||
| chr3:27456278
|
G | A | 1 | a0001c0002t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61-3780C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456278 | ||||||
| chr3:27456527
|
G | A | 10 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-4029C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456527 | ||||||
| chr3:27456598
|
T | G | 1 | a0003c0005t0005g0133 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.61-4100A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456598 | ||||||
| chr3:27456637
|
A | T | 1 | a0001c0001t0001g0294 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.61-4139T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456637 | ||||||
| chr3:27456642
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.61-4144C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456642 | ||||||
| chr3:27456685
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61-4187C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456685 | ||||||
| chr3:27456698
|
G | T | 1 | a0002c0003t0002g0185 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.61-4200C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456698 | ||||||
| chr3:27456841
|
T | TTACCTAA others(10): Show |
1 | a0002c0003t0002g0163 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.61-4360_61-4344dup others(17): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456841 | ||||||
| chr3:27456959
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-4461A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27456959 | ||||||
| chr3:27457201
|
T | G | 22 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0003g0131others(19): Show | 24 | HG00408.hp2 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.61-4703A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457201 | ||||||
| chr3:27457234
|
T | C | 3 | a0001c0001t0015g0087a0001c0001t0015g0088a0001c0002t0011g0048 | 3 | HG01516.hp2 HG03017.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.61-4736A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457234 | ||||||
| chr3:27457253
|
T | C | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-4755A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457253 | ||||||
| chr3:27457435
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.61-4937G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457435 | ||||||
| chr3:27457479
|
T | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02257.hp2 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.61-4981A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457479 | ||||||
| chr3:27457553
|
C | A | 1 | a0001c0001t0001g0291 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.61-5055G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457553 | ||||||
| chr3:27457756
|
A | T | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-5258T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457756 | ||||||
| chr3:27457817
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0010g0105a0001c0001t0010g0113 | 3 | NA18959.hp2 NA18963.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.61-5319T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457817 | ||||||
| chr3:27457942
|
T | C | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.61-5444A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457942 | ||||||
| chr3:27457970
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.61-5472C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27457970 | ||||||
| chr3:27458021
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.61-5523T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458021 | ||||||
| chr3:27458069
|
A | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-5571T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458069 | ||||||
| chr3:27458129
|
A | C | 42 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(39): Show | 42 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-5631T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458129 | ||||||
| chr3:27458188
|
G | GTTTTTAC others(5): Show |
2 | a0002c0003t0002g0164a0002c0003t0002g0165 | 2 | HG02071.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.61-5702_61-5691dup others(12): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458188 | ||||||
| chr3:27458237
|
T | C | 1 | a0001c0001t0003g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.61-5739A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458237 | ||||||
| chr3:27458382
|
G | T | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.61-5884C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458382 | ||||||
| chr3:27458388
|
A | C | 1 | a0001c0002t0004g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.61-5890T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458388 | ||||||
| chr3:27458458
|
T | C | 42 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(39): Show | 42 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-5960A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458458 | ||||||
| chr3:27458497
|
C | T | 42 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(39): Show | 42 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-5999G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458497 | ||||||
| chr3:27458558
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.61-6060A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458558 | ||||||
| chr3:27458578
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-6080A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458578 | ||||||
| chr3:27458804
|
C | T | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-6306G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458804 | ||||||
| chr3:27458853
|
A | G | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-6355T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458853 | ||||||
| chr3:27458982
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-6484C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27458982 | ||||||
| chr3:27459012
|
T | G | 1 | a0001c0001t0003g0111 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.61-6514A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459012 | ||||||
| chr3:27459169
|
C | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.61-6671G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459169 | ||||||
| chr3:27459234
|
A | G | 1 | a0004c0007t0008g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.61-6736T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459234 | ||||||
| chr3:27459326
|
A | G | 1 | a0001c0006t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.61-6828T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459326 | ||||||
| chr3:27459332
|
A | G | 1 | a0001c0004t0006g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.61-6834T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459332 | ||||||
| chr3:27459407
|
GATAAA | G | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.61-6914_61-6910del others(5): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459407 | ||||||
| chr3:27459647
|
T | A | 1 | a0001c0001t0001g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.61-7149A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459647 | ||||||
| chr3:27459648
|
A | T | 1 | a0001c0001t0001g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.61-7150T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459648 | ||||||
| chr3:27459758
|
C | T | 8 | a0003c0005t0005g0138a0003c0005t0005g0140a0003c0005t0005g0142others(5): Show | 8 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-7260G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459758 | ||||||
| chr3:27459800
|
T | C | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.61-7302A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459800 | ||||||
| chr3:27459861
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.61-7363A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459861 | ||||||
| chr3:27459971
|
T | TTA | 8 | a0001c0001t0005g0150a0001c0001t0018g0035a0002c0003t0002g0157others(5): Show | 8 | HG02040.hp1 HG02071.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-7475_61-7474dup others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459971 | ||||||
| chr3:27459971
|
TTA | T | 36 | a0001c0001t0002g0263a0001c0001t0007g0038a0001c0001t0007g0039others(33): Show | 37 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.61-7475_61-7474del others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459971 | ||||||
| chr3:27459971
|
TTATA | T | 7 | a0001c0001t0001g0229a0001c0001t0020g0036a0001c0004t0006g0024others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-7477_61-7474del others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459971 | ||||||
| chr3:27459986
|
T | C | 1 | a0001c0002t0011g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.61-7488A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459986 | ||||||
| chr3:27459986
|
TATATAC | T | 75 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(72): Show | 77 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.61-7494_61-7489del others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459986 | ||||||
| chr3:27459988
|
T | C | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.61-7490A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459988 | ||||||
| chr3:27459988
|
TATAC | T | 62 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0200others(59): Show | 62 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.61-7494_61-7491del others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459988 | ||||||
| chr3:27459990
|
T | C | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-7492A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459990 | ||||||
| chr3:27459990
|
TAC | T | 8 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0003g0090others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-7494_61-7493del others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459990 | ||||||
| chr3:27459992
|
C | T | 55 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(52): Show | 57 | HG00408.hp2 HG00738.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.61-7494G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459992 | ||||||
| chr3:27459994
|
C | T | 37 | a0001c0001t0001g0136a0001c0001t0001g0137a0002c0003t0001g0159others(34): Show | 37 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.61-7496G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27459994 | ||||||
| chr3:27460002
|
C | T | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-7504G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460002 | ||||||
| chr3:27460024
|
C | CAT | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.61-7528_61-7527dup others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460024 | ||||||
| chr3:27460315
|
T | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0136others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.61-7817A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460315 | ||||||
| chr3:27460368
|
A | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-7870T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460368 | ||||||
| chr3:27460393
|
A | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-7895T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460393 | ||||||
| chr3:27460524
|
T | C | 1 | a0001c0004t0006g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.61-8026A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460524 | ||||||
| chr3:27460579
|
G | T | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-8081C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460579 | ||||||
| chr3:27460640
|
C | A | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.61-8142G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460640 | ||||||
| chr3:27460913
|
A | T | 268 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(265): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.61-8415T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27460913 | ||||||
| chr3:27461090
|
G | A | 1 | a0004c0007t0008g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61-8592C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461090 | ||||||
| chr3:27461208
|
G | GCA | 38 | a0001c0001t0001g0106a0001c0001t0001g0136a0001c0001t0001g0137others(35): Show | 40 | HG00408.hp2 HG00639.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.61-8712_61-8711dup others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461208 | ||||||
| chr3:27461208
|
G | GCACA | 16 | a0001c0001t0001g0268a0001c0001t0001g0271a0001c0001t0001g0272others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-8714_61-8711dup others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461208 | ||||||
| chr3:27461208
|
G | GCGCA | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG01109.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.61-8711_61-8710ins others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461208 | ||||||
| chr3:27461208
|
GCA | G | 9 | a0001c0001t0002g0263a0001c0001t0015g0087a0001c0001t0015g0088others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-8712_61-8711del others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461208 | ||||||
| chr3:27461208
|
GCACA | G | 89 | a0001c0001t0001g0194a0001c0001t0003g0095a0001c0001t0007g0038others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.61-8714_61-8711del others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461208 | ||||||
| chr3:27461208
|
GCACACA | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.61-8716_61-8711del others(6): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461208 | ||||||
| chr3:27461278
|
A | T | 7 | a0001c0001t0001g0130a0001c0001t0003g0124a0001c0001t0003g0125others(4): Show | 7 | HG00642.hp1 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-8780T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461278 | ||||||
| chr3:27461330
|
C | T | 1 | a0001c0001t0020g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.61-8832G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461330 | ||||||
| chr3:27461381
|
G | A | 5 | a0001c0002t0012g0050a0001c0002t0012g0051a0001c0002t0012g0066others(2): Show | 5 | NA18953.hp2 NA18956.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-8883C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461381 | ||||||
| chr3:27461428
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-8930G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461428 | ||||||
| chr3:27461583
|
G | A | 1 | a0001c0001t0008g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.61-9085C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461583 | ||||||
| chr3:27461606
|
C | CA | 68 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0277others(65): Show | 69 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.61-9109dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461606 | ||||||
| chr3:27461622
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.61-9124T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461622 | ||||||
| chr3:27461691
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.61-9193C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461691 | ||||||
| chr3:27461751
|
G | A | 1 | a0002c0003t0002g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-9253C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461751 | ||||||
| chr3:27461790
|
T | G | 40 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(37): Show | 40 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.61-9292A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461790 | ||||||
| chr3:27461797
|
CA | C | 14 | a0001c0001t0010g0105a0001c0013t0029g0251a0003c0005t0005g0133others(11): Show | 14 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-9300delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461797 | ||||||
| chr3:27461802
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.61-9304T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461802 | ||||||
| chr3:27461819
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.61-9321C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27461819 | ||||||
| chr3:27462083
|
A | AT | 52 | a0001c0001t0001g0130a0001c0004t0016g0006a0001c0013t0029g0251others(49): Show | 52 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.61-9586dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462083 | ||||||
| chr3:27462187
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-9689A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462187 | ||||||
| chr3:27462224
|
G | A | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-9726C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462224 | ||||||
| chr3:27462270
|
G | A | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-9772C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462270 | ||||||
| chr3:27462367
|
G | A | 2 | a0001c0001t0007g0044a0001c0001t0007g0045 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.61-9869C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462367 | ||||||
| chr3:27462552
|
G | T | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-10054C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462552 | ||||||
| chr3:27462725
|
C | CAT | 268 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(265): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.61-10228_61-10227i others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462725 | ||||||
| chr3:27462828
|
T | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | NA18960.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.61-10330A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462828 | ||||||
| chr3:27462973
|
G | GC | 3 | a0001c0001t0014g0226a0001c0001t0014g0244a0001c0001t0014g0250 | 3 | NA18953.hp1 NA19011.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.61-10476dupG | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27462973 | ||||||
| chr3:27463035
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.61-10537A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463035 | ||||||
| chr3:27463399
|
C | T | 7 | a0001c0001t0011g0052a0001c0002t0011g0053a0001c0002t0011g0054others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-10901G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463399 | ||||||
| chr3:27463531
|
A | C | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-11033T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463531 | ||||||
| chr3:27463536
|
A | T | 1 | a0001c0009t0019g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-11038T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463536 | ||||||
| chr3:27463671
|
C | T | 1 | a0001c0002t0011g0054 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.61-11173G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463671 | ||||||
| chr3:27463672
|
G | A | 21 | a0001c0004t0006g0007a0001c0004t0006g0011a0001c0004t0006g0014others(18): Show | 22 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-11174C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463672 | ||||||
| chr3:27463732
|
G | T | 1 | a0001c0006t0001g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.61-11234C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463732 | ||||||
| chr3:27463826
|
T | A | 1 | a0001c0001t0001g0239 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.61-11328A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463826 | ||||||
| chr3:27463844
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-11346C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463844 | ||||||
| chr3:27463865
|
C | T | 1 | a0001c0001t0007g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61-11367G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27463865 | ||||||
| chr3:27464145
|
G | C | 40 | a0001c0001t0001g0130a0001c0004t0016g0006a0002c0003t0001g0159others(37): Show | 40 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.61-11647C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27464145 | ||||||
| chr3:27464164
|
T | C | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.61-11666A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27464164 | ||||||
| chr3:27464176
|
G | A | 1 | a0002c0003t0002g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.61-11678C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27464176 | ||||||
| chr3:27464460
|
C | G | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-11962G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27464460 | ||||||
| chr3:27464611
|
T | C | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.61-12113A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27464611 | ||||||
| chr3:27464921
|
C | T | 1 | a0001c0004t0016g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61-12423G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27464921 | ||||||
| chr3:27465059
|
A | G | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.61-12561T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465059 | ||||||
| chr3:27465160
|
G | A | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.61-12662C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465160 | ||||||
| chr3:27465287
|
C | A | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-12789G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465287 | ||||||
| chr3:27465289
|
C | CA | 12 | a0001c0001t0001g0137a0001c0001t0015g0087a0001c0001t0018g0035others(9): Show | 12 | HG01192.hp1 HG01433.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-12792dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465289 | ||||||
| chr3:27465289
|
CA | C | 136 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0130others(133): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.61-12792delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465289 | ||||||
| chr3:27465447
|
G | T | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.61-12949C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465447 | ||||||
| chr3:27465474
|
TA | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(153): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.61-12977delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465474 | ||||||
| chr3:27465474
|
TAA | T | 69 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(66): Show | 69 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.61-12978_61-12977d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465474 | ||||||
| chr3:27465496
|
T | C | 1 | a0004c0007t0008g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.61-12998A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465496 | ||||||
| chr3:27465688
|
C | A | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.61-13190G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465688 | ||||||
| chr3:27465821
|
G | A | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-13323C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465821 | ||||||
| chr3:27465881
|
G | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02257.hp2 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.61-13383C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465881 | ||||||
| chr3:27465886
|
G | A | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.61-13388C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465886 | ||||||
| chr3:27465893
|
G | C | 54 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(51): Show | 54 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.61-13395C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465893 | ||||||
| chr3:27465953
|
C | CA | 6 | a0001c0001t0001g0190a0001c0001t0001g0292a0001c0001t0005g0149others(3): Show | 6 | HG02074.hp2 HG03130.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-13456dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465953 | ||||||
| chr3:27465953
|
CAA | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-13457_61-13456d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465953 | ||||||
| chr3:27465964
|
AAAGAAAG | A | 36 | a0001c0001t0002g0115a0001c0001t0003g0090a0001c0001t0003g0091others(33): Show | 36 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.61-13473_61-13467d others(9): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465964 | ||||||
| chr3:27465965
|
AAG | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-13469_61-13468d others(4): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465965 | ||||||
| chr3:27465965
|
AAGAAAG | A | 6 | a0001c0001t0001g0106a0001c0001t0003g0108a0001c0001t0010g0105others(3): Show | 6 | HG06807.hp1 NA18906.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-13473_61-13468d others(8): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465965 | ||||||
| chr3:27465966
|
AG | A | 4 | a0001c0001t0001g0239a0001c0002t0011g0053a0001c0002t0012g0050others(1): Show | 4 | HG01074.hp1 HG01167.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-13469delC | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465966 | ||||||
| chr3:27465967
|
G | A | 150 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(147): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.61-13469C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465967 | ||||||
| chr3:27465967
|
G | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-13469C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465967 | ||||||
| chr3:27465971
|
G | A | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.61-13473C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465971 | ||||||
| chr3:27465979
|
G | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG03704.hp1 HG03834.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61-13481C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27465979 | ||||||
| chr3:27466004
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.61-13506C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466004 | ||||||
| chr3:27466032
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-13534A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466032 | ||||||
| chr3:27466190
|
G | A | 1 | a0002c0003t0002g0172 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.61-13692C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466190 | ||||||
| chr3:27466227
|
G | A | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.61-13729C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466227 | ||||||
| chr3:27466319
|
T | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-13821A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466319 | ||||||
| chr3:27466431
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.61-13933C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466431 | ||||||
| chr3:27466448
|
T | C | 1 | a0001c0001t0005g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.61-13950A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466448 | ||||||
| chr3:27466448
|
T | G | 1 | a0003c0005t0005g0147 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.61-13950A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466448 | ||||||
| chr3:27466449
|
C | CA | 21 | a0001c0001t0001g0137a0001c0001t0001g0264a0001c0001t0001g0265others(18): Show | 21 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-13952dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466449 | ||||||
| chr3:27466449
|
CA | C | 82 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.61-13952delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466449 | ||||||
| chr3:27466482
|
T | C | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.61-13984A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466482 | ||||||
| chr3:27466492
|
CA | C | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.61-13995delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466492 | ||||||
| chr3:27466585
|
T | C | 268 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(265): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.61-14087A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466585 | ||||||
| chr3:27466623
|
T | C | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.61-14125A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466623 | ||||||
| chr3:27466626
|
G | A | 19 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 21 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.61-14128C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466626 | ||||||
| chr3:27466786
|
G | A | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-14288C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466786 | ||||||
| chr3:27466806
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.61-14308C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466806 | ||||||
| chr3:27466807
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61-14309G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466807 | ||||||
| chr3:27466842
|
G | C | 4 | a0001c0004t0013g0008a0001c0004t0013g0009a0001c0004t0013g0010others(1): Show | 4 | HG01243.hp2 HG01934.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-14344C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466842 | ||||||
| chr3:27466870
|
T | A | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.61-14372A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466870 | ||||||
| chr3:27466871
|
T | G | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-14373A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466871 | ||||||
| chr3:27466892
|
T | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-14394A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466892 | ||||||
| chr3:27466916
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.61-14418C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466916 | ||||||
| chr3:27466954
|
G | A | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.61-14456C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27466954 | ||||||
| chr3:27467079
|
G | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-14581C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467079 | ||||||
| chr3:27467129
|
A | G | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-14631T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467129 | ||||||
| chr3:27467174
|
C | T | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-14676G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467174 | ||||||
| chr3:27467224
|
C | T | 1 | a0001c0001t0018g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.61-14726G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467224 | ||||||
| chr3:27467468
|
C | G | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.61-14970G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467468 | ||||||
| chr3:27467589
|
A | G | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-15091T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467589 | ||||||
| chr3:27467619
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-15121A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27467619 | ||||||
| chr3:27468149
|
G | C | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(17): Show | 22 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-15651C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468149 | ||||||
| chr3:27468223
|
G | C | 144 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.61-15725C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468223 | ||||||
| chr3:27468226
|
G | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02257.hp2 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.61-15728C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468226 | ||||||
| chr3:27468355
|
A | T | 1 | a0003c0005t0005g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.60+15712T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468355 | ||||||
| chr3:27468434
|
G | C | 4 | a0001c0001t0003g0092a0001c0001t0003g0109a0001c0001t0003g0110others(1): Show | 4 | HG00673.hp1 NA18977.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+15633C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468434 | ||||||
| chr3:27468519
|
A | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.60+15548T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468519 | ||||||
| chr3:27468737
|
G | T | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+15330C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468737 | ||||||
| chr3:27468813
|
A | G | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+15254T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468813 | ||||||
| chr3:27468819
|
T | C | 1 | a0001c0018t0004g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.60+15248A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27468819 | ||||||
| chr3:27469038
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.60+15029G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469038 | ||||||
| chr3:27469114
|
G | GA | 39 | a0001c0004t0016g0006a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+14952dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469114 | ||||||
| chr3:27469200
|
C | T | 1 | a0001c0001t0015g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.60+14867G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469200 | ||||||
| chr3:27469201
|
G | A | 1 | a0001c0001t0024g0202 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.60+14866C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469201 | ||||||
| chr3:27469246
|
C | A | 65 | a0001c0001t0001g0089a0001c0001t0001g0130a0001c0001t0001g0189others(62): Show | 66 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.60+14821G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469246 | ||||||
| chr3:27469315
|
A | C | 1 | a0001c0001t0011g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.60+14752T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469315 | ||||||
| chr3:27469325
|
G | A | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.60+14742C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469325 | ||||||
| chr3:27469368
|
G | A | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+14699C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469368 | ||||||
| chr3:27469430
|
G | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+14637C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469430 | ||||||
| chr3:27469727
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.60+14340A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469727 | ||||||
| chr3:27469959
|
A | G | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | HG02965.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+14108T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27469959 | ||||||
| chr3:27470054
|
T | C | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+14013A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470054 | ||||||
| chr3:27470076
|
A | C | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+13991T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470076 | ||||||
| chr3:27470172
|
T | C | 3 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122 | 3 | HG00280.hp1 HG01175.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.60+13895A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470172 | ||||||
| chr3:27470262
|
G | C | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+13805C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470262 | ||||||
| chr3:27470641
|
T | TA | 50 | a0001c0001t0018g0035a0001c0004t0016g0006a0002c0003t0001g0159others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+13425dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470641 | ||||||
| chr3:27470652
|
A | AC | 94 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(91): Show | 96 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.60+13414_60+13415i others(3): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470652 | ||||||
| chr3:27470804
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.60+13263A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470804 | ||||||
| chr3:27470873
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+13194G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470873 | ||||||
| chr3:27470897
|
G | A | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+13170C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470897 | ||||||
| chr3:27470970
|
A | G | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+13097T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470970 | ||||||
| chr3:27470982
|
C | A | 3 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0095 | 3 | HG00741.hp2 HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.60+13085G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27470982 | ||||||
| chr3:27471055
|
C | T | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+13012G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471055 | ||||||
| chr3:27471100
|
T | C | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+12967A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471100 | ||||||
| chr3:27471101
|
A | G | 1 | a0001c0004t0006g0011 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.60+12966T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471101 | ||||||
| chr3:27471146
|
C | T | 3 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0095 | 3 | HG00741.hp2 HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.60+12921G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471146 | ||||||
| chr3:27471404
|
G | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(76): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.60+12663C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471404 | ||||||
| chr3:27471453
|
G | A | 40 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(37): Show | 40 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.60+12614C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471453 | ||||||
| chr3:27471468
|
A | G | 268 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(265): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.60+12599T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471468 | ||||||
| chr3:27471480
|
C | T | 40 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(37): Show | 40 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.60+12587G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471480 | ||||||
| chr3:27471533
|
T | C | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+12534A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471533 | ||||||
| chr3:27471631
|
C | G | 1 | a0001c0004t0013g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.60+12436G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471631 | ||||||
| chr3:27471835
|
A | G | 1 | a0001c0004t0009g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.60+12232T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471835 | ||||||
| chr3:27471875
|
C | A | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+12192G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471875 | ||||||
| chr3:27471909
|
G | A | 1 | a0001c0002t0004g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.60+12158C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471909 | ||||||
| chr3:27471986
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.60+12081G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27471986 | ||||||
| chr3:27472172
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.60+11895C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472172 | ||||||
| chr3:27472227
|
A | C | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.60+11840T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472227 | ||||||
| chr3:27472424
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.60+11643A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472424 | ||||||
| chr3:27472449
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.60+11618A>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472449 | ||||||
| chr3:27472453
|
C | A | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+11614G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472453 | ||||||
| chr3:27472503
|
T | C | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.60+11564A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472503 | ||||||
| chr3:27472519
|
AATAAC | A | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+11543_60+11547d others(7): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472519 | ||||||
| chr3:27472524
|
C | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+11543G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472524 | ||||||
| chr3:27472570
|
C | G | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.60+11497G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472570 | ||||||
| chr3:27472891
|
C | G | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+11176G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472891 | ||||||
| chr3:27472899
|
G | C | 1 | a0001c0002t0004g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.60+11168C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27472899 | ||||||
| chr3:27473079
|
C | CA | 47 | a0001c0001t0001g0106a0001c0001t0001g0189a0001c0001t0001g0279others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.60+10987dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473079 | ||||||
| chr3:27473079
|
CA | C | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+10987delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473079 | ||||||
| chr3:27473106
|
G | C | 1 | a0002c0003t0002g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60+10961C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473106 | ||||||
| chr3:27473269
|
C | A | 35 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(32): Show | 35 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.60+10798G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473269 | ||||||
| chr3:27473275
|
G | A | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+10792C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473275 | ||||||
| chr3:27473416
|
A | G | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.60+10651T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473416 | ||||||
| chr3:27473450
|
G | C | 1 | a0001c0001t0003g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.60+10617C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473450 | ||||||
| chr3:27473480
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.60+10587C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473480 | ||||||
| chr3:27473493
|
G | A | 12 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+10574C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473493 | ||||||
| chr3:27473562
|
G | T | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.60+10505C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473562 | ||||||
| chr3:27473652
|
G | A | 18 | a0001c0001t0005g0135a0001c0001t0005g0149a0001c0001t0018g0035others(15): Show | 20 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.60+10415C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473652 | ||||||
| chr3:27473656
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.60+10411G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473656 | ||||||
| chr3:27473705
|
C | CA | 19 | a0001c0001t0001g0282a0001c0001t0005g0149a0001c0001t0005g0150others(16): Show | 19 | HG00738.hp1 HG01074.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.60+10361dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473705 | ||||||
| chr3:27473705
|
CA | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(127): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.60+10361delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473705 | ||||||
| chr3:27473770
|
T | C | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+10297A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473770 | ||||||
| chr3:27473780
|
C | G | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+10287G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473780 | ||||||
| chr3:27473780
|
C | T | 1 | a0001c0001t0003g0118 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.60+10287G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473780 | ||||||
| chr3:27473817
|
C | T | 42 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(39): Show | 42 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.60+10250G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473817 | ||||||
| chr3:27473845
|
G | A | 1 | a0008c0015t0022g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.60+10222C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27473845 | ||||||
| chr3:27474009
|
G | A | 1 | a0001c0004t0006g0018 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.60+10058C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474009 | ||||||
| chr3:27474010
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.60+10057A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474010 | ||||||
| chr3:27474063
|
C | T | 1 | a0003c0005t0005g0148 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.60+10004G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474063 | ||||||
| chr3:27474235
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+9832T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474235 | ||||||
| chr3:27474263
|
C | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+9804G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474263 | ||||||
| chr3:27474363
|
A | C | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+9704T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474363 | ||||||
| chr3:27474379
|
A | G | 51 | a0001c0004t0016g0006a0001c0013t0029g0251a0002c0003t0001g0159others(48): Show | 51 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+9688T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474379 | ||||||
| chr3:27474439
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.60+9628A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474439 | ||||||
| chr3:27474537
|
C | CG | 3 | a0001c0001t0018g0035a0001c0002t0012g0050a0001c0002t0012g0051 | 3 | NA18989.hp2 NA19011.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.60+9529dupC | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474537 | ||||||
| chr3:27474538
|
G | A | 5 | a0001c0001t0002g0115a0001c0001t0003g0116a0001c0001t0003g0117others(2): Show | 5 | HG02698.hp2 HG03490.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+9529C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474538 | ||||||
| chr3:27474697
|
G | C | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+9370C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474697 | ||||||
| chr3:27474721
|
G | A | 1 | a0001c0004t0009g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.60+9346C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474721 | ||||||
| chr3:27474850
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.60+9217C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474850 | ||||||
| chr3:27474927
|
G | A | 19 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(16): Show | 19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.60+9140C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474927 | ||||||
| chr3:27474935
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.60+9132G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27474935 | ||||||
| chr3:27475184
|
C | G | 2 | a0001c0001t0015g0087a0001c0001t0015g0088 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.60+8883G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27475184 | ||||||
| chr3:27475362
|
G | T | 50 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(47): Show | 50 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+8705C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27475362 | ||||||
| chr3:27475769
|
G | C | 1 | a0001c0002t0011g0048 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.60+8298C>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27475769 | ||||||
| chr3:27475896
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.60+8171C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27475896 | ||||||
| chr3:27475980
|
A | G | 1 | a0001c0004t0016g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60+8087T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27475980 | ||||||
| chr3:27476029
|
C | A | 1 | a0001c0004t0006g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.60+8038G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27476029 | ||||||
| chr3:27476676
|
C | A | 91 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.60+7391G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27476676 | ||||||
| chr3:27476684
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.60+7383G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27476684 | ||||||
| chr3:27476884
|
A | T | 1 | a0001c0001t0005g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.60+7183T>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27476884 | ||||||
| chr3:27477070
|
C | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(264): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.60+6997G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477070 | ||||||
| chr3:27477482
|
C | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+6585G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477482 | ||||||
| chr3:27477547
|
G | A | 1 | a0001c0013t0029g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.60+6520C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477547 | ||||||
| chr3:27477642
|
T | TC | 5 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(2): Show | 5 | HG00673.hp2 HG02074.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+6424dupG | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477642 | ||||||
| chr3:27477667
|
C | T | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+6400G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477667 | ||||||
| chr3:27477704
|
G | A | 144 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.60+6363C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477704 | ||||||
| chr3:27477815
|
G | A | 1 | a0001c0006t0001g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.60+6252C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477815 | ||||||
| chr3:27477991
|
C | A | 11 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.60+6076G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27477991 | ||||||
| chr3:27478007
|
C | G | 1 | a0001c0006t0001g0193 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.60+6060G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478007 | ||||||
| chr3:27478061
|
T | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+6006A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478061 | ||||||
| chr3:27478199
|
G | A | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+5868C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478199 | ||||||
| chr3:27478202
|
GA | G | 41 | a0001c0001t0011g0052a0001c0001t0020g0036a0001c0002t0004g0060others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.60+5864delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478202 | ||||||
| chr3:27478202
|
GAA | G | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.60+5863_60+5864del others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478202 | ||||||
| chr3:27478204
|
A | G | 40 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+5863T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478204 | ||||||
| chr3:27478248
|
T | C | 1 | a0001c0004t0006g0018 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.60+5819A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478248 | ||||||
| chr3:27478270
|
C | A | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+5797G>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478270 | ||||||
| chr3:27478273
|
T | A | 1 | a0002c0003t0002g0183 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.60+5794A>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478273 | ||||||
| chr3:27478391
|
G | A | 38 | a0002c0003t0001g0159a0002c0003t0001g0162a0002c0003t0002g0151others(35): Show | 38 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.60+5676C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478391 | ||||||
| chr3:27478426
|
G | T | 11 | a0004c0007t0001g0254a0004c0007t0008g0252a0004c0007t0008g0253others(8): Show | 11 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+5641C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478426 | ||||||
| chr3:27478501
|
G | A | 1 | a0001c0004t0006g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.60+5566C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478501 | ||||||
| chr3:27478511
|
C | CA | 77 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0264others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.60+5555dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478511 | ||||||
| chr3:27478511
|
C | CAA | 6 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0013t0029g0251others(3): Show | 6 | HG01192.hp1 HG01891.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+5554_60+5555dup others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478511 | ||||||
| chr3:27478511
|
CA | C | 15 | a0001c0001t0001g0246a0001c0001t0005g0149a0001c0001t0020g0036others(12): Show | 15 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.60+5555delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478511 | ||||||
| chr3:27478525
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.60+5542T>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478525 | ||||||
| chr3:27478616
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG01952.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.60+5451G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478616 | ||||||
| chr3:27478800
|
C | T | 1 | a0005c0008t0002g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.60+5267G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478800 | ||||||
| chr3:27478805
|
T | C | 1 | a0001c0004t0016g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60+5262A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478805 | ||||||
| chr3:27478833
|
C | CA | 64 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0282others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.60+5233dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478833 | ||||||
| chr3:27478833
|
CA | C | 6 | a0001c0001t0001g0192a0001c0001t0001g0285a0001c0001t0003g0092others(3): Show | 6 | HG01070.hp2 HG02602.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+5233delT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478833 | ||||||
| chr3:27478849
|
A | G | 13 | a0001c0001t0001g0191a0001c0001t0002g0263a0004c0007t0001g0254others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.60+5218T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478849 | ||||||
| chr3:27478868
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.60+5199C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27478868 | ||||||
| chr3:27479008
|
G | GA | 41 | a0001c0001t0005g0149a0001c0004t0006g0022a0001c0004t0016g0006others(38): Show | 41 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+5058dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479008 | ||||||
| chr3:27479009
|
A | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(97): Show | 102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.60+5058T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479009 | ||||||
| chr3:27479364
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.60+4703A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479364 | ||||||
| chr3:27479423
|
C | CA | 100 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(97): Show | 102 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.60+4643dupT | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479423 | ||||||
| chr3:27479423
|
C | CAA | 52 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.60+4642_60+4643dup others(2): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479423 | ||||||
| chr3:27479557
|
T | C | 53 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.60+4510A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479557 | ||||||
| chr3:27479733
|
T | C | 268 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(265): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.60+4334A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479733 | ||||||
| chr3:27479747
|
C | T | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.60+4320G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27479747 | ||||||
| chr3:27480156
|
T | C | 4 | a0001c0002t0004g0082a0001c0002t0004g0083a0001c0002t0004g0084others(1): Show | 4 | HG02965.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+3911A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480156 | ||||||
| chr3:27480393
|
A | G | 22 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0003g0131others(19): Show | 24 | HG00408.hp2 HG02027.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.60+3674T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480393 | ||||||
| chr3:27480501
|
G | A | 2 | a0001c0002t0004g0085a0001c0002t0004g0086 | 2 | HG01433.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.60+3566C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480501 | ||||||
| chr3:27480507
|
G | T | 39 | a0001c0013t0029g0251a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+3560C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480507 | ||||||
| chr3:27480620
|
T | C | 15 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.60+3447A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480620 | ||||||
| chr3:27480629
|
G | A | 39 | a0001c0001t0011g0052a0001c0002t0004g0060a0001c0002t0004g0061others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.60+3438C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480629 | ||||||
| chr3:27480672
|
G | A | 4 | a0001c0004t0009g0001a0001c0004t0009g0032a0001c0004t0009g0033others(1): Show | 5 | HG02486.hp2 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+3395C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480672 | ||||||
| chr3:27480917
|
G | T | 268 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0106others(265): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.60+3150C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27480917 | ||||||
| chr3:27481209
|
T | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(76): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.60+2858A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27481209 | ||||||
| chr3:27481252
|
A | AT | 80 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0130others(77): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.60+2814dupA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27481252 | ||||||
| chr3:27481404
|
AT | A | 6 | a0001c0001t0003g0124a0001c0001t0003g0125a0001c0001t0003g0126others(3): Show | 6 | HG01255.hp1 HG01257.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+2662delA | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27481404 | ||||||
| chr3:27481683
|
T | C | 12 | a0001c0004t0006g0024a0001c0004t0006g0025a0001c0004t0006g0028others(9): Show | 13 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.60+2384A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27481683 | ||||||
| chr3:27481784
|
C | G | 41 | a0001c0001t0001g0106a0001c0001t0002g0115a0001c0001t0003g0090others(38): Show | 41 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.60+2283G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27481784 | ||||||
| chr3:27481966
|
T | C | 39 | a0001c0004t0016g0006a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+2101A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27481966 | ||||||
| chr3:27482128
|
G | A | 51 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+1939C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27482128 | ||||||
| chr3:27482163
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.60+1904A>G | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27482163 | ||||||
| chr3:27482420
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.60+1647G>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27482420 | ||||||
| chr3:27482667
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0001g0285a0001c0001t0001g0286others(10): Show | 13 | HG02027.hp2 NA18942.hp1 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.60+1400C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27482667 | ||||||
| chr3:27482773
|
A | AAAT | 39 | a0001c0004t0016g0006a0002c0003t0001g0159a0002c0003t0001g0162others(36): Show | 39 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.60+1291_60+1293dup others(3): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27482773 | ||||||
| chr3:27483136
|
A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.60+931T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483136 | ||||||
| chr3:27483284
|
C | T | 3 | a0003c0005t0005g0002a0003c0005t0005g0133a0003c0005t0005g0134 | 4 | NA18993.hp1 NA19007.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+783G>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483284 | ||||||
| chr3:27483562
|
G | A | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.60+505C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483562 | ||||||
| chr3:27483566
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.60+501C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483566 | ||||||
| chr3:27483749
|
A | G | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0005g0135others(18): Show | 23 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.60+318T>C | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483749 | ||||||
| chr3:27483862
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.60+205C>T | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483862 | ||||||
| chr3:27483912
|
GGGGATGG others(3): Show |
G | 43 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0002g0115others(40): Show | 43 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.60+145_60+154delTC others(8): Show |
SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483912 | ||||||
| chr3:27483943
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.60+124C>A | SLC4A7 | ENSG00000033867.18 | transcript | ENST00000454389.6 | protein_coding | 1/25 | chr3 | 27483943 |