| geneid | 9498 |
|---|---|
| ensemblid | ENSG00000050438.17 |
| hgncid | 11034 |
| symbol | SLC4A8 |
| name | solute carrier family 4 member 8 |
| refseq_nuc | NM_001039960.3 |
| refseq_prot | NP_001035049.1 |
| ensembl_nuc | ENST00000453097.7 |
| ensembl_prot | ENSP00000405812.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51424831 |
| end | 51515763 |
| strand | + |
| ver | v1.2 |
| region | chr12:51424831-51515763 |
| region5000 | chr12:51419831-51520763 |
| regionname0 | SLC4A8_chr12_51424831_51515763 |
| regionname5000 | SLC4A8_chr12_51419831_51520763 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1093 | 353 | 90 | 59 | 154 | 14 | 34 | 114 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0002 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0003 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0004 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0005 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0006 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3282 | 312 | 71 | 57 | 138 | 14 | 30 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0002 | 0/0 | 3282 | 26 | 10 | 0 | 14 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0003 | 0/0 | 3282 | 7 | 7 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0004 | 0/0 | 3282 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0005 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0006 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0007 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0008 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0009 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0010 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0011 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0012 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0013 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0014 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| c0015 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8481 | 97 | 15 | 21 | 48 | 4 | 9 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0002 | 0/1 | 8482 | 67 | 11 | 22 | 16 | 6 | 11 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0003 | 1/0 | 8483 | 42 | 8 | 8 | 18 | 2 | 5 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0004 | 0/0 | 8482 | 34 | 3 | 2 | 26 | 1 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0005 | 0/0 | 8482 | 25 | 9 | 0 | 14 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0006 | 0/0 | 8482 | 8 | 8 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0007 | 0/0 | 8482 | 5 | 1 | 0 | 4 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0008 | 0/0 | 8481 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0009 | 0/0 | 8481 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0010 | 0/0 | 8483 | 4 | 4 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0011 | 0/0 | 8481 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0012 | 0/0 | 8481 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0013 | 0/0 | 8483 | 3 | 1 | 1 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0014 | 0/0 | 8482 | 3 | 2 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0015 | 0/0 | 8482 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0016 | 0/0 | 8484 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0017 | 0/0 | 8481 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0018 | 0/0 | 8481 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0019 | 0/0 | 8481 | 2 | 0 | 0 | 0 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0020 | 0/0 | 8481 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0021 | 0/0 | 8483 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0022 | 0/0 | 8482 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0023 | 0/0 | 8481 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0024 | 0/0 | 8482 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0025 | 0/0 | 8483 | 2 | 1 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0026 | 0/0 | 8481 | 2 | 0 | 0 | 0 | 1 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0027 | 0/0 | 8482 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0028 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0029 | 0/0 | 8481 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0030 | 0/0 | 8481 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0031 | 0/0 | 8481 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0032 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0033 | 0/0 | 8481 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0034 | 0/0 | 8481 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0035 | 0/0 | 8481 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0036 | 0/0 | 8483 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0037 | 0/0 | 8483 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0038 | 0/0 | 8483 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0039 | 0/0 | 8482 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0040 | 0/0 | 8481 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0041 | 0/0 | 8482 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0042 | 0/0 | 8482 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0043 | 0/0 | 8482 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0044 | 0/0 | 8482 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0045 | 0/0 | 8483 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0046 | 0/0 | 8481 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0047 | 0/0 | 8482 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0048 | 0/0 | 8482 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0049 | 0/0 | 8482 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0050 | 0/0 | 8482 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0051 | 0/0 | 8482 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0052 | 0/0 | 8482 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| t0053 | 0/0 | 8481 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| 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 | 3 | 0 | 2 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0333 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3282 | 312 | 71 | 57 | 138 | 14 | 30 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0002 | 0/0 | 3282 | 26 | 10 | 0 | 14 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0003 | 0/0 | 3282 | 7 | 7 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0004 | 0/0 | 3282 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0005 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0006 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0008 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0010 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0011 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0014 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0002c0013 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0003c0007 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0004c0009 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0005c0012 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0006c0015 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11762 | 94 | 14 | 21 | 47 | 4 | 8 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0002 | 0/1 | 11763 | 64 | 10 | 20 | 16 | 6 | 11 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0003 | 1/0 | 11764 | 39 | 8 | 7 | 17 | 2 | 4 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0004 | 0/0 | 11763 | 34 | 3 | 2 | 26 | 1 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0006 | 0/0 | 11763 | 8 | 8 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0007 | 0/0 | 11763 | 5 | 1 | 0 | 4 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0008 | 0/0 | 11762 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0009 | 0/0 | 11762 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0011 | 0/0 | 11762 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0012 | 0/0 | 11762 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0013 | 0/0 | 11764 | 2 | 0 | 1 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0014 | 0/0 | 11763 | 3 | 2 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0015 | 0/0 | 11763 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0016 | 0/0 | 11765 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0017 | 0/0 | 11762 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0018 | 0/0 | 11762 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0019 | 0/0 | 11762 | 2 | 0 | 0 | 0 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0020 | 0/0 | 11762 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0021 | 0/0 | 11764 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0022 | 0/0 | 11763 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0023 | 0/0 | 11762 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0024 | 0/0 | 11763 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0025 | 0/0 | 11764 | 2 | 1 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0026 | 0/0 | 11762 | 2 | 0 | 0 | 0 | 1 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0028 | 0/0 | 11762 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0029 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0030 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0031 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0032 | 0/0 | 11762 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0033 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0034 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0035 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0037 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0038 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0039 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0040 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0041 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0042 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0043 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0048 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0049 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0050 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0051 | 0/0 | 11763 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0052 | 0/0 | 11763 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0001t0053 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0002t0005 | 0/0 | 11763 | 18 | 3 | 0 | 13 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0002t0010 | 0/0 | 11764 | 4 | 4 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0002t0027 | 0/0 | 11763 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0002t0044 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0002t0045 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0003t0005 | 0/0 | 11763 | 6 | 6 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0003t0046 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0004t0002 | 0/0 | 11763 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0005t0005 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0006t0002 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0008t0036 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0010t0001 | 0/0 | 11762 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0011t0047 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0001c0014t0003 | 0/0 | 11764 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0002c0013t0003 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0003c0007t0003 | 0/0 | 11764 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0004c0009t0013 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0005c0012t0001 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| a0006c0015t0001 | 0/0 | 11762 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | copy fasta | chr12 | 51419831 | 51520763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0333 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0011g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0012g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0012g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0012g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0014g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0015g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0016g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0016g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0017g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0017g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0018g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0018g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0019g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0019g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0020g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0020g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0021g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0021g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0022g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0022g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0023g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0023g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0024g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0024g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0025g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0026g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0026g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0028g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0029g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0030g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0031g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0032g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0033g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0034g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0035g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0037g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0038g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0039g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0040g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0041g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0042g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0043g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0048g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0049g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0050g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0051g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0052g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0001t0053g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0027g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0027g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0044g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0002t0045g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0003t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0003t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0003t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0003t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0003t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0003t0046g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0004t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0004t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0005t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0006t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0008t0036g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0010t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0011t0047g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0001c0014t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0002c0013t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0003c0007t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0004c0009t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0005c0012t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| a0006c0015t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0321 | EUR | FIN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00423 | hp1 | a0001 | c0001 | t0032 | g0296 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00544 | hp2 | a0001 | c0001 | t0048 | g0022 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00558 | hp2 | a0001 | c0002 | t0005 | g0163 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00609 | hp1 | a0001 | c0001 | t0015 | g0136 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00639 | hp2 | a0001 | c0001 | t0031 | g0264 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00642 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00733 | hp2 | a0001 | c0001 | t0030 | g0189 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0126 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01192 | hp2 | a0001 | c0001 | t0035 | g0218 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0312 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01261 | hp2 | a0001 | c0004 | t0002 | g0109 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0328 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0115 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0046 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01517 | hp1 | a0001 | c0001 | t0026 | g0047 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01884 | hp1 | a0001 | c0001 | t0037 | g0346 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01884 | hp2 | a0001 | c0002 | t0010 | g0019 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01891 | hp1 | a0001 | c0002 | t0010 | g0152 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01891 | hp2 | a0001 | c0001 | t0025 | g0026 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01928 | hp2 | a0003 | c0007 | t0003 | g0310 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01978 | hp2 | a0001 | c0001 | t0014 | g0103 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02015 | hp2 | a0001 | c0001 | t0039 | g0098 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0155 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0211 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02071 | hp1 | a0001 | c0001 | t0025 | g0023 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02071 | hp2 | a0001 | c0002 | t0005 | g0158 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02083 | hp1 | a0001 | c0002 | t0005 | g0161 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02257 | hp1 | a0001 | c0002 | t0027 | g0297 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0178 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02300 | hp2 | a0001 | c0001 | t0034 | g0221 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02572 | hp1 | a0001 | c0003 | t0005 | g0181 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0085 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0157 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02622 | hp2 | a0001 | c0006 | t0002 | g0119 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02630 | hp2 | a0001 | c0003 | t0005 | g0006 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02723 | hp1 | a0001 | c0002 | t0044 | g0299 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02723 | hp2 | a0001 | c0003 | t0005 | g0006 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02735 | hp1 | a0001 | c0014 | t0003 | g0327 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02809 | hp1 | a0001 | c0001 | t0022 | g0154 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0291 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02818 | hp1 | a0001 | c0001 | t0023 | g0070 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0176 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02895 | hp2 | a0001 | c0002 | t0010 | g0151 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0180 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02897 | hp1 | a0001 | c0002 | t0010 | g0150 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02897 | hp2 | a0001 | c0003 | t0046 | g0182 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0265 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0016 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0331 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02976 | hp2 | a0001 | c0001 | t0014 | g0015 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03098 | hp1 | a0001 | c0001 | t0040 | g0145 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0279 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03130 | hp1 | a0001 | c0001 | t0020 | g0332 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03225 | hp1 | a0001 | c0008 | t0036 | g0068 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0286 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0179 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03516 | hp2 | a0001 | c0001 | t0033 | g0249 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03669 | hp1 | a0001 | c0001 | t0019 | g0216 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03704 | hp2 | a0001 | c0001 | t0019 | g0217 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03831 | hp1 | a0001 | c0002 | t0005 | g0170 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03831 | hp2 | a0001 | c0001 | t0051 | g0057 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0329 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03927 | hp2 | a0001 | c0010 | t0001 | g0220 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04204 | hp1 | a0001 | c0001 | t0052 | g0045 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04204 | hp2 | a0001 | c0002 | t0005 | g0159 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04228 | hp1 | a0001 | c0001 | t0026 | g0050 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0303 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18522 | hp2 | a0005 | c0012 | t0001 | g0014 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18906 | hp2 | a0001 | c0001 | t0021 | g0156 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18941 | hp2 | a0001 | c0002 | t0005 | g0164 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18943 | hp1 | a0001 | c0001 | t0041 | g0128 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18943 | hp2 | a0001 | c0001 | t0016 | g0344 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18944 | hp1 | a0001 | c0001 | t0050 | g0040 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18944 | hp2 | a0001 | c0001 | t0038 | g0010 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18950 | hp2 | a0001 | c0002 | t0005 | g0168 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18953 | hp2 | a0001 | c0001 | t0015 | g0135 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18962 | hp1 | a0001 | c0002 | t0005 | g0169 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18963 | hp2 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18966 | hp2 | a0001 | c0002 | t0005 | g0175 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18970 | hp1 | a0001 | c0001 | t0049 | g0033 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18974 | hp1 | a0001 | c0001 | t0015 | g0075 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18978 | hp1 | a0001 | c0001 | t0012 | g0270 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18978 | hp2 | a0001 | c0005 | t0005 | g0160 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18979 | hp1 | a0001 | c0001 | t0011 | g0197 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18979 | hp2 | a0001 | c0002 | t0005 | g0166 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18981 | hp2 | a0001 | c0001 | t0024 | g0110 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18983 | hp2 | a0001 | c0002 | t0005 | g0174 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18988 | hp2 | a0001 | c0002 | t0005 | g0171 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18989 | hp2 | a0001 | c0001 | t0018 | g0285 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18997 | hp1 | a0001 | c0011 | t0047 | g0167 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18997 | hp2 | a0001 | c0001 | t0013 | g0095 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19004 | hp1 | a0001 | c0001 | t0017 | g0256 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19004 | hp2 | a0001 | c0001 | t0011 | g0199 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19011 | hp2 | a0002 | c0013 | t0003 | g0309 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19012 | hp1 | a0001 | c0001 | t0028 | g0239 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19012 | hp2 | a0001 | c0002 | t0005 | g0165 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0203 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19030 | hp2 | a0001 | c0001 | t0053 | g0084 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19054 | hp2 | a0001 | c0001 | t0018 | g0275 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19056 | hp2 | a0001 | c0001 | t0011 | g0198 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19060 | hp2 | a0001 | c0001 | t0012 | g0212 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19063 | hp1 | a0006 | c0015 | t0001 | g0338 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19068 | hp1 | a0001 | c0002 | t0005 | g0173 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0191 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19079 | hp1 | a0001 | c0002 | t0005 | g0162 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19080 | hp1 | a0001 | c0001 | t0012 | g0282 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19081 | hp2 | a0001 | c0001 | t0017 | g0255 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19082 | hp2 | a0001 | c0001 | t0016 | g0343 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19086 | hp2 | a0001 | c0001 | t0024 | g0118 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0140 | EUR | TSI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | GIH | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0330 | SAS | GIH | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01123 | hp1 | a0001 | c0001 | t0029 | g0278 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0177 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02486 | hp1 | a0004 | c0009 | t0013 | g0077 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG02559 | hp2 | a0001 | c0001 | t0023 | g0147 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG03471 | hp2 | a0001 | c0001 | t0022 | g0153 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG06807 | hp1 | a0001 | c0001 | t0043 | g0149 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| HG06807 | hp2 | a0001 | c0002 | t0027 | g0298 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA18955 | hp2 | a0001 | c0002 | t0045 | g0172 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| NA21309 | hp2 | a0001 | c0001 | t0042 | g0148 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0138 | REF | REF | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0333 | REF | REF | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51457438
|
A | G | 1 | a0006 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.662A>G | p.His221Arg | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/25 | 819/11764 | 662/3282 | 221/1093 | chr12 | 51457438 | ||
| chr12:51462342
|
G | T | 1 | a0002 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1134G>T | p.Glu378Asp | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/25 | 1291/11764 | 1134/3282 | 378/1093 | chr12 | 51462342 | ||
| chr12:51462443
|
A | G | 1 | a0005 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1235A>G | p.Asn412Ser | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/25 | 1392/11764 | 1235/3282 | 412/1093 | chr12 | 51462443 | ||
| chr12:51474421
|
G | A | 1 | a0003 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1984G>A | p.Val662Ile | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 15/25 | 2141/11764 | 1984/3282 | 662/1093 | chr12 | 51474421 | ||
| chr12:51489943
|
A | G | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2692A>G | p.Ile898Val | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/25 | 2849/11764 | 2692/3282 | 898/1093 | chr12 | 51489943 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51450910
|
G | C | 1 | a0001c0005 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.165G>C | p.Pro55Pro | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/25 | 322/11764 | 165/3282 | 55/1093 | chr12 | 51450910 | ||
| chr12:51460076
|
C | G | 1 | a0001c0003 | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.981C>G | p.Leu327Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/25 | 1138/11764 | 981/3282 | 327/1093 | chr12 | 51460076 | ||
| chr12:51461225
|
T | G | 1 | a0001c0006 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1035T>G | p.Gly345Gly | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/25 | 1192/11764 | 1035/3282 | 345/1093 | chr12 | 51461225 | ||
| chr12:51461276
|
C | G | 1 | a0001c0014 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1086C>G | p.Thr362Thr | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/25 | 1243/11764 | 1086/3282 | 362/1093 | chr12 | 51461276 | ||
| chr12:51462375
|
C | T | 1 | a0001c0004 | 2 | HG01081.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.1167C>T | p.Phe389Phe | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/25 | 1324/11764 | 1167/3282 | 389/1093 | chr12 | 51462375 | ||
| chr12:51469653
|
C | G | 4 | a0001c0002a0001c0003a0001c0005others(1): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
synonymous_variant | LOW | c.1389C>G | p.Ala463Ala | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 12/25 | 1546/11764 | 1389/3282 | 463/1093 | chr12 | 51469653 | ||
| chr12:51469759
|
C | T | 4 | a0001c0002a0001c0003a0001c0005others(1): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
synonymous_variant | LOW | c.1495C>T | p.Leu499Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 12/25 | 1652/11764 | 1495/3282 | 499/1093 | chr12 | 51469759 | ||
| chr12:51488788
|
C | G | 1 | a0001c0010 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.2376C>G | p.Leu792Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/25 | 2533/11764 | 2376/3282 | 792/1093 | chr12 | 51488788 | ||
| chr12:51489915
|
G | C | 1 | a0001c0008 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.2664G>C | p.Leu888Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/25 | 2821/11764 | 2664/3282 | 888/1093 | chr12 | 51489915 | ||
| chr12:51494977
|
C | T | 4 | a0001c0002a0001c0003a0001c0005others(1): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
synonymous_variant | LOW | c.2802C>T | p.Pro934Pro | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/25 | 2959/11764 | 2802/3282 | 934/1093 | chr12 | 51494977 | ||
| chr12:51494986
|
C | T | 1 | a0001c0011 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.2811C>T | p.His937His | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/25 | 2968/11764 | 2811/3282 | 937/1093 | chr12 | 51494986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51424884
|
G | T | 1 | a0001c0002t0027 | 2 | HG02257.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-104G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/25 | 104 | chr12 | 51424884 | |||||
| chr12:51507606
|
A | G | 35 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(32): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 168 | chr12 | 51507606 | |||||
| chr12:51507651
|
A | T | 2 | a0001c0001t0009a0001c0001t0053 | 6 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*213A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 213 | chr12 | 51507651 | |||||
| chr12:51507914
|
G | C | 15 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(12): Show | 97 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*476G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 476 | chr12 | 51507914 | |||||
| chr12:51508031
|
C | T | 1 | a0001c0001t0038 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 593 | chr12 | 51508031 | |||||
| chr12:51508211
|
T | C | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(56): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*773T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 773 | chr12 | 51508211 | |||||
| chr12:51508257
|
T | C | 1 | a0001c0001t0039 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 819 | chr12 | 51508257 | |||||
| chr12:51508414
|
C | T | 2 | a0001c0001t0021a0001c0001t0022 | 4 | HG02055.hp2 HG02809.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*976C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 976 | chr12 | 51508414 | |||||
| chr12:51508440
|
AG | A | 20 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(17): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1004delG | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1004 | INFO_REALIGN_3_PRIME | chr12 | 51508440 | ||||
| chr12:51508465
|
C | T | 10 | a0001c0001t0004a0001c0001t0012a0001c0001t0016others(7): Show | 49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1027C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1027 | chr12 | 51508465 | |||||
| chr12:51508469
|
A | ATT | 1 | a0001c0001t0016 | 3 | NA18943.hp2 NA18963.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032_*1033insTT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1033 | INFO_REALIGN_3_PRIME | chr12 | 51508469 | ||||
| chr12:51508717
|
T | C | 1 | a0001c0001t0028 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1279 | chr12 | 51508717 | |||||
| chr12:51509087
|
C | T | 1 | a0001c0001t0015 | 3 | HG00609.hp1 NA18953.hp2 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1649C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1649 | chr12 | 51509087 | |||||
| chr12:51509420
|
C | T | 1 | a0001c0001t0035 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1982C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1982 | chr12 | 51509420 | |||||
| chr12:51509721
|
C | G | 1 | a0001c0001t0011 | 3 | NA18979.hp1 NA19004.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2283C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2283 | chr12 | 51509721 | |||||
| chr12:51509768
|
T | C | 1 | a0001c0001t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2330 | chr12 | 51509768 | |||||
| chr12:51509831
|
A | T | 3 | a0001c0001t0021a0001c0001t0022a0001c0001t0037 | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2393A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2393 | chr12 | 51509831 | |||||
| chr12:51509896
|
G | A | 1 | a0001c0002t0010 | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2458G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2458 | chr12 | 51509896 | |||||
| chr12:51509953
|
G | A | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG06807.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2515 | chr12 | 51509953 | |||||
| chr12:51509954
|
A | T | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG06807.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2516A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2516 | chr12 | 51509954 | |||||
| chr12:51509979
|
G | A | 2 | a0001c0002t0027a0001c0002t0044 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2541G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2541 | chr12 | 51509979 | |||||
| chr12:51510060
|
C | T | 1 | a0001c0001t0052 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2622C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2622 | chr12 | 51510060 | |||||
| chr12:51510076
|
C | G | 11 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(8): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2638C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2638 | chr12 | 51510076 | |||||
| chr12:51510152
|
C | T | 1 | a0001c0001t0034 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2714C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2714 | chr12 | 51510152 | |||||
| chr12:51510241
|
G | A | 1 | a0001c0008t0036 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2803G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2803 | chr12 | 51510241 | |||||
| chr12:51510253
|
C | T | 1 | a0001c0011t0047 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2815C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2815 | chr12 | 51510253 | |||||
| chr12:51510423
|
CA | C | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(41): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*3006delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3006 | INFO_REALIGN_3_PRIME | chr12 | 51510423 | ||||
| chr12:51510423
|
CAA | C | 6 | a0001c0001t0009a0001c0001t0023a0001c0001t0026others(3): Show | 12 | HG01517.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3005_*3006delAA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3005 | INFO_REALIGN_3_PRIME | chr12 | 51510423 | ||||
| chr12:51510456
|
G | A | 1 | a0001c0001t0029 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3018G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3018 | chr12 | 51510456 | |||||
| chr12:51510858
|
G | A | 1 | a0001c0001t0048 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3420G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3420 | chr12 | 51510858 | |||||
| chr12:51511032
|
C | T | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3594C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3594 | chr12 | 51511032 | |||||
| chr12:51511075
|
T | C | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(56): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*3637T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3637 | chr12 | 51511075 | |||||
| chr12:51511167
|
T | C | 1 | a0001c0001t0053 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3729T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3729 | chr12 | 51511167 | |||||
| chr12:51511247
|
G | A | 1 | a0001c0001t0050 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3809G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3809 | chr12 | 51511247 | |||||
| chr12:51511401
|
T | A | 2 | a0001c0001t0014a0001c0001t0029 | 4 | HG01123.hp1 HG01978.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3963T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3963 | chr12 | 51511401 | |||||
| chr12:51511593
|
T | C | 1 | a0001c0001t0037 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4155T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4155 | chr12 | 51511593 | |||||
| chr12:51511824
|
C | T | 8 | a0001c0002t0005a0001c0002t0027a0001c0002t0044others(5): Show | 31 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4386C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4386 | chr12 | 51511824 | |||||
| chr12:51511879
|
G | A | 1 | a0001c0001t0030 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4441G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4441 | chr12 | 51511879 | |||||
| chr12:51511891
|
C | T | 1 | a0001c0001t0024 | 2 | NA18981.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4453C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4453 | chr12 | 51511891 | |||||
| chr12:51512261
|
G | A | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*4823G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4823 | chr12 | 51512261 | |||||
| chr12:51512296
|
G | C | 1 | a0001c0001t0017 | 2 | NA19004.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4858 | chr12 | 51512296 | |||||
| chr12:51512457
|
T | C | 1 | a0001c0001t0041 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5019T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5019 | chr12 | 51512457 | |||||
| chr12:51512513
|
C | G | 1 | a0001c0001t0033 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5075C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5075 | chr12 | 51512513 | |||||
| chr12:51512565
|
C | A | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(56): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*5127C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5127 | chr12 | 51512565 | |||||
| chr12:51512736
|
T | G | 1 | a0001c0001t0051 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5298T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5298 | chr12 | 51512736 | |||||
| chr12:51512962
|
G | T | 1 | a0001c0001t0006 | 8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5524G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5524 | chr12 | 51512962 | |||||
| chr12:51512980
|
T | G | 1 | a0001c0001t0018 | 2 | NA18989.hp2 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5542T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5542 | chr12 | 51512980 | |||||
| chr12:51513216
|
G | A | 1 | a0001c0001t0019 | 2 | HG03669.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5778G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5778 | chr12 | 51513216 | |||||
| chr12:51513400
|
T | C | 35 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(32): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*5962T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5962 | chr12 | 51513400 | |||||
| chr12:51513414
|
G | A | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*5976G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5976 | chr12 | 51513414 | |||||
| chr12:51513643
|
T | C | 1 | a0001c0002t0010 | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6205T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6205 | chr12 | 51513643 | |||||
| chr12:51513699
|
C | T | 1 | a0001c0001t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6261C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6261 | chr12 | 51513699 | |||||
| chr12:51513896
|
C | A | 1 | a0001c0002t0010 | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6458C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6458 | chr12 | 51513896 | |||||
| chr12:51513969
|
A | G | 1 | a0001c0001t0032 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6531A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6531 | chr12 | 51513969 | |||||
| chr12:51514509
|
T | G | 1 | a0001c0001t0031 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7071T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7071 | chr12 | 51514509 | |||||
| chr12:51514820
|
G | A | 11 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(8): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*7382G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7382 | chr12 | 51514820 | |||||
| chr12:51514879
|
G | C | 1 | a0001c0001t0020 | 2 | HG02976.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7441G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7441 | chr12 | 51514879 | |||||
| chr12:51514912
|
G | A | 1 | a0001c0001t0008 | 5 | HG02258.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7474G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7474 | chr12 | 51514912 | |||||
| chr12:51515055
|
C | T | 1 | a0001c0002t0027 | 2 | HG02257.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7617C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7617 | chr12 | 51515055 | |||||
| chr12:51515348
|
G | C | 20 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(17): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*7910G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7910 | chr12 | 51515348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51425044
|
CCGCCTCC others(2): Show |
C | 4 | a0001c0001t0004g0345a0001c0001t0016g0343a0001c0001t0016g0344others(1): Show | 4 | HG01884.hp1 NA18943.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+20_48+28delGCCT others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51425044 | |||||
| chr12:51425106
|
T | A | 4 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(1): Show | 4 | HG02922.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+71T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425106 | ||||||
| chr12:51425142
|
TC | T | 5 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(2): Show | 5 | HG02523.hp1 NA18962.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+110delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51425142 | |||||
| chr12:51425250
|
G | C | 4 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(1): Show | 4 | HG02922.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+215G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425250 | ||||||
| chr12:51425255
|
T | C | 2 | a0001c0001t0014g0015a0001c0001t0014g0016 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.48+220T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425255 | ||||||
| chr12:51425365
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.48+330C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425365 | ||||||
| chr12:51425643
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.48+608G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425643 | ||||||
| chr12:51425670
|
G | C | 1 | a0001c0002t0010g0019 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.48+635G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425670 | ||||||
| chr12:51425848
|
A | C | 1 | a0005c0012t0001g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+813A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425848 | ||||||
| chr12:51425900
|
C | T | 1 | a0001c0001t0003g0336 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.48+865C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425900 | ||||||
| chr12:51426128
|
C | G | 1 | a0001c0001t0002g0335 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.48+1093C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426128 | ||||||
| chr12:51426170
|
G | A | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.48+1135G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426170 | ||||||
| chr12:51426331
|
C | T | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.48+1296C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426331 | ||||||
| chr12:51426496
|
G | A | 46 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.48+1461G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426496 | ||||||
| chr12:51426715
|
G | A | 6 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+1680G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426715 | ||||||
| chr12:51426827
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.48+1792G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426827 | ||||||
| chr12:51426920
|
ATTTTCTT others(9): Show |
A | 1 | a0001c0001t0032g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.48+1901_48+1916del others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51426920 | |||||
| chr12:51426941
|
CT | C | 6 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(3): Show | 6 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+1921delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51426941 | |||||
| chr12:51426995
|
G | T | 1 | a0001c0001t0002g0295 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.48+1960G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426995 | ||||||
| chr12:51427026
|
T | C | 183 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(180): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.48+1991T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427026 | ||||||
| chr12:51427095
|
C | A | 1 | a0001c0001t0003g0300 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.48+2060C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427095 | ||||||
| chr12:51427174
|
G | A | 1 | a0001c0001t0004g0021 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.48+2139G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427174 | ||||||
| chr12:51427221
|
A | G | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+2186A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427221 | ||||||
| chr12:51427755
|
A | G | 21 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(18): Show | 21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.48+2720A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427755 | ||||||
| chr12:51427831
|
C | T | 1 | a0001c0002t0005g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.48+2796C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427831 | ||||||
| chr12:51427897
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.48+2862C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427897 | ||||||
| chr12:51427900
|
A | G | 39 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(36): Show | 40 | HG00558.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.48+2865A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427900 | ||||||
| chr12:51428043
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.48+3008C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428043 | ||||||
| chr12:51428141
|
A | G | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+3106A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428141 | ||||||
| chr12:51428259
|
C | G | 47 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(44): Show | 47 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.48+3224C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428259 | ||||||
| chr12:51428435
|
A | G | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+3400A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428435 | ||||||
| chr12:51428481
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.48+3446A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428481 | ||||||
| chr12:51428591
|
A | T | 47 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(44): Show | 47 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.48+3556A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428591 | ||||||
| chr12:51428660
|
A | G | 49 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(46): Show | 49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.48+3625A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428660 | ||||||
| chr12:51429023
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG00621.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.48+3988C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429023 | ||||||
| chr12:51429234
|
G | A | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.48+4199G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429234 | ||||||
| chr12:51429242
|
G | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+4207G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429242 | ||||||
| chr12:51429261
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.48+4226G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429261 | ||||||
| chr12:51429335
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.48+4300A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429335 | ||||||
| chr12:51429459
|
C | T | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+4424C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429459 | ||||||
| chr12:51429516
|
T | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+4481T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429516 | ||||||
| chr12:51429584
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.48+4549C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429584 | ||||||
| chr12:51429613
|
C | G | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.48+4578C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429613 | ||||||
| chr12:51429668
|
A | C | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+4633A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429668 | ||||||
| chr12:51429705
|
C | T | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.48+4670C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429705 | ||||||
| chr12:51429709
|
A | G | 49 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(46): Show | 49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.48+4674A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429709 | ||||||
| chr12:51430133
|
A | G | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48+5098A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430133 | ||||||
| chr12:51430232
|
T | C | 28 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.48+5197T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430232 | ||||||
| chr12:51430362
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.48+5327G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430362 | ||||||
| chr12:51430524
|
G | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+5489G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430524 | ||||||
| chr12:51430583
|
A | G | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.48+5548A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430583 | ||||||
| chr12:51430640
|
C | T | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.48+5605C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430640 | ||||||
| chr12:51430643
|
G | C | 1 | a0001c0001t0048g0022 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.48+5608G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430643 | ||||||
| chr12:51430653
|
G | A | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.48+5618G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430653 | ||||||
| chr12:51430670
|
C | A | 1 | a0001c0001t0025g0023 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.48+5635C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430670 | ||||||
| chr12:51431082
|
A | G | 1 | a0001c0003t0005g0006 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.48+6047A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51431082 | ||||||
| chr12:51431212
|
C | T | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+6177C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51431212 | ||||||
| chr12:51431604
|
A | AT | 42 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0028others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+6579dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51431604 | |||||
| chr12:51431956
|
T | A | 1 | a0001c0002t0005g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48+6921T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51431956 | ||||||
| chr12:51432033
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.48+6998T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432033 | ||||||
| chr12:51432137
|
G | A | 1 | a0001c0001t0004g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.48+7102G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432137 | ||||||
| chr12:51432283
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.48+7248C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432283 | ||||||
| chr12:51432294
|
C | T | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+7259C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432294 | ||||||
| chr12:51432303
|
C | T | 1 | a0001c0001t0043g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+7268C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432303 | ||||||
| chr12:51432410
|
C | CA | 161 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.48+7393dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51432410 | |||||
| chr12:51432410
|
C | CAA | 90 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(87): Show | 91 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.48+7392_48+7393dup others(2): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51432410 | |||||
| chr12:51432474
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.48+7439C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432474 | ||||||
| chr12:51432535
|
G | A | 5 | a0001c0001t0003g0009a0001c0001t0003g0300a0001c0001t0003g0302others(2): Show | 6 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+7500G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432535 | ||||||
| chr12:51432646
|
C | T | 1 | a0001c0003t0005g0181 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.48+7611C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432646 | ||||||
| chr12:51432719
|
C | T | 1 | a0001c0001t0023g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48+7684C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432719 | ||||||
| chr12:51432755
|
C | A | 1 | a0004c0009t0013g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+7720C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432755 | ||||||
| chr12:51432764
|
A | G | 1 | a0001c0001t0006g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48+7729A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432764 | ||||||
| chr12:51432769
|
T | C | 7 | a0001c0001t0006g0003a0001c0001t0006g0011a0001c0001t0006g0012others(4): Show | 8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+7734T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432769 | ||||||
| chr12:51432910
|
T | C | 1 | a0001c0001t0003g0305 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49-7798T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432910 | ||||||
| chr12:51432938
|
T | G | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49-7770T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432938 | ||||||
| chr12:51433335
|
C | T | 179 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(176): Show | 184 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.49-7373C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433335 | ||||||
| chr12:51433559
|
T | G | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-7149T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433559 | ||||||
| chr12:51433771
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49-6937G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433771 | ||||||
| chr12:51433826
|
G | T | 1 | a0001c0001t0021g0156 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.49-6882G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433826 | ||||||
| chr12:51433828
|
C | G | 1 | a0001c0001t0021g0156 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.49-6880C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433828 | ||||||
| chr12:51433851
|
G | GT | 31 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0190others(28): Show | 31 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.49-6830dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433851 | |||||
| chr12:51433851
|
GT | G | 33 | a0001c0001t0001g0194a0001c0001t0001g0247a0001c0001t0001g0260others(30): Show | 35 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-6830delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433851 | |||||
| chr12:51433851
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.49-6839_49-6830del others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433851 | |||||
| chr12:51433861
|
T | G | 10 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(7): Show | 11 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.49-6847T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433861 | ||||||
| chr12:51433862
|
T | G | 145 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(142): Show | 149 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.49-6846T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433862 | ||||||
| chr12:51433866
|
T | G | 64 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0301others(61): Show | 67 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.49-6842T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433866 | ||||||
| chr12:51433867
|
T | G | 145 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(142): Show | 149 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.49-6841T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433867 | ||||||
| chr12:51433868
|
TTTTTTTT others(5): Show |
T | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-6837_49-6826del others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433868 | |||||
| chr12:51433869
|
TTTTTTTT others(4): Show |
T | 145 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(142): Show | 149 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.49-6836_49-6826del others(11): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433869 | |||||
| chr12:51433871
|
T | G | 1 | a0001c0001t0003g0306 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49-6837T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433871 | ||||||
| chr12:51433875
|
T | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0187a0001c0001t0001g0247others(14): Show | 17 | HG00597.hp1 HG00642.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.49-6833T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433875 | ||||||
| chr12:51433875
|
T | TG | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0258others(1): Show | 4 | HG00140.hp2 HG02109.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-6833_49-6832ins others(1): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433875 | ||||||
| chr12:51433880
|
G | T | 168 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(165): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.49-6828G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433880 | ||||||
| chr12:51433884
|
G | T | 347 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(344): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.49-6824G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433884 | ||||||
| chr12:51433887
|
T | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0184others(1): Show | 4 | HG00642.hp1 HG01993.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-6821T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433887 | ||||||
| chr12:51433934
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.49-6774G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433934 | ||||||
| chr12:51434153
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0261 | 2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.49-6555G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434153 | ||||||
| chr12:51434331
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.49-6377G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434331 | ||||||
| chr12:51434481
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49-6227A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434481 | ||||||
| chr12:51434516
|
G | A | 6 | a0001c0001t0009g0071a0001c0001t0009g0081a0001c0001t0009g0082others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-6192G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434516 | ||||||
| chr12:51434814
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.49-5894C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434814 | ||||||
| chr12:51434845
|
A | G | 1 | a0001c0001t0043g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.49-5863A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434845 | ||||||
| chr12:51435022
|
G | C | 1 | a0001c0001t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.49-5686G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435022 | ||||||
| chr12:51435073
|
A | T | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.49-5635A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435073 | ||||||
| chr12:51435326
|
T | C | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-5382T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435326 | ||||||
| chr12:51435588
|
C | T | 1 | a0001c0001t0003g0305 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49-5120C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435588 | ||||||
| chr12:51435589
|
G | A | 3 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0295 | 3 | HG00733.hp1 HG00735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.49-5119G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435589 | ||||||
| chr12:51435678
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49-5030A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435678 | ||||||
| chr12:51435748
|
G | C | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49-4960G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435748 | ||||||
| chr12:51435762
|
T | C | 1 | a0001c0001t0003g0302 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.49-4946T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435762 | ||||||
| chr12:51435863
|
C | T | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-4845C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435863 | ||||||
| chr12:51435877
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | NA18970.hp2 NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.49-4831C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435877 | ||||||
| chr12:51436026
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.49-4682A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436026 | ||||||
| chr12:51436037
|
A | G | 9 | a0001c0001t0002g0144a0001c0001t0009g0071a0001c0001t0009g0081others(6): Show | 9 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.49-4671A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436037 | ||||||
| chr12:51436115
|
T | G | 1 | a0001c0001t0003g0308 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.49-4593T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436115 | ||||||
| chr12:51436321
|
A | G | 28 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.49-4387A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436321 | ||||||
| chr12:51436493
|
A | G | 1 | a0001c0001t0004g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.49-4215A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436493 | ||||||
| chr12:51436606
|
G | GTTAT | 6 | a0001c0001t0001g0227a0001c0001t0001g0257a0001c0001t0003g0330others(3): Show | 6 | HG00597.hp1 HG02080.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-4086_49-4083dup others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51436606 | |||||
| chr12:51436622
|
TTTAG | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0257a0001c0001t0003g0330others(3): Show | 6 | HG00597.hp1 HG02080.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-4070_49-4067del others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51436622 | |||||
| chr12:51436772
|
G | A | 4 | a0001c0001t0006g0011a0001c0001t0006g0012a0001c0001t0006g0013others(1): Show | 4 | HG02895.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-3936G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436772 | ||||||
| chr12:51437353
|
A | G | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-3355A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437353 | ||||||
| chr12:51437438
|
A | G | 28 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.49-3270A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437438 | ||||||
| chr12:51437475
|
A | C | 2 | a0001c0002t0005g0174a0001c0002t0005g0175 | 2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.49-3233A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437475 | ||||||
| chr12:51437985
|
A | T | 1 | a0001c0001t0040g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49-2723A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437985 | ||||||
| chr12:51437987
|
G | A | 126 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.49-2721G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437987 | ||||||
| chr12:51438055
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.49-2653G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438055 | ||||||
| chr12:51438203
|
A | G | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.49-2505A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438203 | ||||||
| chr12:51438312
|
C | T | 1 | a0001c0001t0007g0191 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.49-2396C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438312 | ||||||
| chr12:51438501
|
T | A | 14 | a0001c0001t0002g0004a0001c0001t0002g0080a0001c0001t0002g0089others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-2207T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438501 | ||||||
| chr12:51438676
|
C | A | 1 | a0001c0001t0002g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.49-2032C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438676 | ||||||
| chr12:51438720
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.49-1988C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438720 | ||||||
| chr12:51438756
|
G | C | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.49-1952G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438756 | ||||||
| chr12:51438771
|
A | G | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.49-1937A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438771 | ||||||
| chr12:51438817
|
A | T | 1 | a0001c0001t0006g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49-1891A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438817 | ||||||
| chr12:51438907
|
T | C | 1 | a0001c0001t0040g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49-1801T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438907 | ||||||
| chr12:51438911
|
CTATT | C | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-1795_49-1792del others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51438911 | |||||
| chr12:51439087
|
C | T | 126 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(123): Show | 128 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.49-1621C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439087 | ||||||
| chr12:51439294
|
T | G | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49-1414T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439294 | ||||||
| chr12:51439311
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49-1397C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439311 | ||||||
| chr12:51439611
|
T | TA | 7 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 7 | HG00280.hp1 HG01255.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-1086dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51439611 | |||||
| chr12:51439969
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49-739A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439969 | ||||||
| chr12:51440224
|
G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.49-484G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440224 | ||||||
| chr12:51440279
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.49-429A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440279 | ||||||
| chr12:51440403
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.49-305T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440403 | ||||||
| chr12:51440410
|
GT | G | 176 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(173): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.49-283delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51440410 | |||||
| chr12:51440440
|
C | T | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.49-268C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440440 | ||||||
| chr12:51441207
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0244 | 2 | HG01975.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.130+418C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441207 | ||||||
| chr12:51441400
|
T | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.130+611T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441400 | ||||||
| chr12:51441476
|
T | C | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.130+687T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441476 | ||||||
| chr12:51441698
|
A | G | 3 | a0001c0002t0005g0171a0001c0002t0005g0173a0001c0002t0045g0172 | 3 | NA18955.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.130+909A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441698 | ||||||
| chr12:51441715
|
C | G | 1 | a0001c0001t0008g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+926C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441715 | ||||||
| chr12:51441793
|
G | A | 48 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(45): Show | 48 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.130+1004G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441793 | ||||||
| chr12:51441799
|
G | A | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+1010G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441799 | ||||||
| chr12:51441958
|
A | C | 28 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+1169A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441958 | ||||||
| chr12:51442476
|
C | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.130+1687C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442476 | ||||||
| chr12:51442487
|
A | G | 347 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(344): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.130+1698A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442487 | ||||||
| chr12:51442515
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0008g0262 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.130+1726G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442515 | ||||||
| chr12:51442641
|
G | A | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.130+1852G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442641 | ||||||
| chr12:51442832
|
C | T | 183 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(180): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.130+2043C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442832 | ||||||
| chr12:51442839
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.130+2050C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442839 | ||||||
| chr12:51443093
|
A | G | 1 | a0001c0001t0002g0140 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.130+2304A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443093 | ||||||
| chr12:51443268
|
C | T | 1 | a0001c0001t0040g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130+2479C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443268 | ||||||
| chr12:51443275
|
C | T | 2 | a0001c0001t0018g0275a0001c0001t0018g0285 | 2 | NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.130+2486C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443275 | ||||||
| chr12:51443836
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+3047C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443836 | ||||||
| chr12:51443894
|
A | G | 1 | a0001c0002t0005g0170 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.130+3105A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443894 | ||||||
| chr12:51444005
|
T | C | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.130+3216T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444005 | ||||||
| chr12:51444030
|
T | C | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+3241T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444030 | ||||||
| chr12:51444359
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.130+3570C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444359 | ||||||
| chr12:51444422
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+3633A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444422 | ||||||
| chr12:51444505
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0225a0001c0001t0001g0243others(2): Show | 5 | HG00438.hp2 HG00621.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+3716A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444505 | ||||||
| chr12:51444680
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130+3891G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444680 | ||||||
| chr12:51444718
|
T | C | 12 | a0001c0001t0003g0002a0001c0001t0003g0301a0001c0001t0003g0311others(9): Show | 14 | HG00673.hp1 HG00735.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+3929T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444718 | ||||||
| chr12:51444881
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.130+4092A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444881 | ||||||
| chr12:51445125
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.130+4336C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445125 | ||||||
| chr12:51445350
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+4561T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445350 | ||||||
| chr12:51445579
|
C | T | 1 | a0001c0002t0005g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130+4790C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445579 | ||||||
| chr12:51445620
|
G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0290a0001c0001t0020g0331others(1): Show | 4 | HG01346.hp1 HG02257.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+4831G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445620 | ||||||
| chr12:51445853
|
AC | A | 179 | a0001c0001t0001g0261a0001c0001t0002g0001a0001c0001t0002g0004others(176): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.131-5015delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51445853 | |||||
| chr12:51446019
|
T | A | 3 | a0001c0001t0011g0197a0001c0001t0011g0198a0001c0001t0011g0199 | 3 | NA18979.hp1 NA19004.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.131-4857T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446019 | ||||||
| chr12:51446036
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG01346.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.131-4840A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446036 | ||||||
| chr12:51446363
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.131-4513C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446363 | ||||||
| chr12:51446547
|
AAAG | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4321_131-4319d others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51446547 | |||||
| chr12:51446619
|
C | T | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4257C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446619 | ||||||
| chr12:51446751
|
T | C | 1 | a0001c0001t0001g0007 | 2 | NA18980.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.131-4125T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446751 | ||||||
| chr12:51446906
|
C | T | 1 | a0001c0001t0051g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.131-3970C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446906 | ||||||
| chr12:51446959
|
G | C | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.131-3917G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446959 | ||||||
| chr12:51446969
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.131-3907A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446969 | ||||||
| chr12:51447036
|
G | C | 1 | a0001c0001t0040g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.131-3840G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447036 | ||||||
| chr12:51447048
|
G | GTCTGTCT others(5): Show |
41 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0072others(38): Show | 44 | HG00099.hp2 HG00544.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447048 | |||||
| chr12:51447052
|
G | GTCTATCT others(1): Show |
47 | a0001c0001t0002g0004a0001c0001t0002g0089a0001c0001t0002g0090others(44): Show | 47 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | |||||
| chr12:51447052
|
G | GTCTATCT others(9): Show |
20 | a0001c0001t0002g0076a0001c0001t0002g0100a0001c0001t0002g0101others(17): Show | 20 | HG00280.hp1 HG00741.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(18): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | |||||
| chr12:51447052
|
G | GTCTATCT others(13): Show |
15 | a0001c0001t0002g0063a0001c0001t0002g0066a0001c0001t0002g0067others(12): Show | 15 | HG00639.hp1 HG01978.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(22): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | |||||
| chr12:51447052
|
G | GTCTATCT others(17): Show |
8 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0134others(5): Show | 9 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(26): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | |||||
| chr12:51447052
|
G | GTCTATCT others(21): Show |
2 | a0001c0001t0002g0064a0001c0001t0002g0065 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.131-3821_131-3820i others(30): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | |||||
| chr12:51447056
|
G | A | 97 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0063others(94): Show | 101 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.131-3820G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447056 | ||||||
| chr12:51447060
|
A | ATCTG | 10 | a0001c0001t0004g0029a0001c0001t0009g0071a0001c0001t0009g0081others(7): Show | 10 | HG02071.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-3813_131-3812i others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447060 | |||||
| chr12:51447064
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.131-3812A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447064 | ||||||
| chr12:51447064
|
ATCTG | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | NA18970.hp2 NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.131-3808_131-3805d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447064 | |||||
| chr12:51447068
|
G | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.131-3808G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447068 | ||||||
| chr12:51447068
|
G | GTCTA | 20 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(17): Show | 21 | HG00558.hp1 HG00597.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-3787_131-3784d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447068 | |||||
| chr12:51447071
|
T | G | 1 | a0001c0001t0004g0061 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.131-3805T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447071 | ||||||
| chr12:51447099
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.131-3777G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447099 | ||||||
| chr12:51447130
|
G | A | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.131-3746G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447130 | ||||||
| chr12:51447460
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.131-3416G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447460 | ||||||
| chr12:51447479
|
A | C | 1 | a0005c0012t0001g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.131-3397A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447479 | ||||||
| chr12:51447647
|
G | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3229G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447647 | ||||||
| chr12:51447714
|
C | CT | 35 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0002g0097others(32): Show | 37 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.131-3142dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447714 | |||||
| chr12:51447714
|
C | CTT | 43 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(40): Show | 43 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.131-3143_131-3142d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447714 | |||||
| chr12:51447714
|
CT | C | 32 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0290others(29): Show | 32 | HG00558.hp2 HG01346.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.131-3142delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447714 | |||||
| chr12:51447774
|
T | C | 2 | a0001c0001t0042g0148a0001c0001t0043g0149 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.131-3102T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447774 | ||||||
| chr12:51447877
|
C | T | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.131-2999C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447877 | ||||||
| chr12:51447909
|
C | T | 5 | a0001c0001t0004g0020a0001c0001t0004g0046a0001c0001t0004g0048others(2): Show | 5 | HG01099.hp2 HG01167.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2967C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447909 | ||||||
| chr12:51447966
|
G | A | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2910G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447966 | ||||||
| chr12:51448136
|
T | C | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-2740T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448136 | ||||||
| chr12:51448189
|
A | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.131-2687A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448189 | ||||||
| chr12:51448385
|
A | G | 1 | a0001c0001t0004g0062 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.131-2491A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448385 | ||||||
| chr12:51448724
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-2152G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448724 | ||||||
| chr12:51448758
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.131-2118A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448758 | ||||||
| chr12:51448816
|
C | T | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.131-2060C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448816 | ||||||
| chr12:51448966
|
G | A | 1 | a0001c0001t0023g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-1910G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448966 | ||||||
| chr12:51449281
|
C | CA | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1588dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51449281 | |||||
| chr12:51449324
|
G | T | 1 | a0001c0002t0005g0169 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131-1552G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449324 | ||||||
| chr12:51449435
|
G | GA | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.131-1428dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51449435 | |||||
| chr12:51449534
|
C | T | 28 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-1342C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449534 | ||||||
| chr12:51449578
|
T | A | 1 | a0001c0001t0007g0263 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.131-1298T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449578 | ||||||
| chr12:51449702
|
G | A | 1 | a0001c0001t0025g0023 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.131-1174G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449702 | ||||||
| chr12:51449799
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.131-1077C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449799 | ||||||
| chr12:51449854
|
C | T | 8 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 8 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-1022C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449854 | ||||||
| chr12:51450067
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0290 | 2 | HG01346.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.131-809A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450067 | ||||||
| chr12:51450470
|
G | A | 3 | a0001c0001t0003g0308a0001c0001t0003g0320a0001c0001t0003g0336 | 3 | HG00609.hp2 NA18971.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.131-406G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450470 | ||||||
| chr12:51450715
|
A | G | 22 | a0001c0001t0002g0004a0001c0001t0002g0089a0001c0001t0002g0090others(19): Show | 22 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-161A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450715 | ||||||
| chr12:51450831
|
T | A | 1 | a0001c0001t0026g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-45T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450831 | ||||||
| chr12:51451123
|
C | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.277+101C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451123 | ||||||
| chr12:51451164
|
G | T | 3 | a0001c0001t0002g0144a0001c0001t0023g0147a0001c0001t0040g0145 | 3 | HG02559.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.277+142G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451164 | ||||||
| chr12:51451274
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.277+252G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451274 | ||||||
| chr12:51451383
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.277+361G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451383 | ||||||
| chr12:51451429
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.277+407T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451429 | ||||||
| chr12:51451584
|
C | G | 1 | a0001c0002t0005g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.278-540C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451584 | ||||||
| chr12:51451633
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.278-491A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451633 | ||||||
| chr12:51451666
|
G | T | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.278-458G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451666 | ||||||
| chr12:51451911
|
C | T | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.278-213C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451911 | ||||||
| chr12:51451918
|
T | G | 1 | a0001c0002t0010g0019 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.278-206T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451918 | ||||||
| chr12:51452020
|
G | A | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-104G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51452020 | ||||||
| chr12:51452023
|
G | A | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-101G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51452023 | ||||||
| chr12:51452306
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.413+47G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452306 | ||||||
| chr12:51452346
|
T | A | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.413+87T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452346 | ||||||
| chr12:51452371
|
A | G | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.413+112A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452371 | ||||||
| chr12:51452448
|
A | G | 3 | a0001c0001t0021g0155a0001c0001t0022g0153a0001c0001t0022g0154 | 3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.413+189A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452448 | ||||||
| chr12:51452477
|
T | C | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.413+218T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452477 | ||||||
| chr12:51452491
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.413+232A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452491 | ||||||
| chr12:51452653
|
C | G | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+394C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452653 | ||||||
| chr12:51452659
|
G | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG00642.hp2 HG01496.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+400G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452659 | ||||||
| chr12:51452758
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.413+499G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452758 | ||||||
| chr12:51452768
|
T | A | 1 | a0001c0001t0002g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.413+509T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452768 | ||||||
| chr12:51452768
|
T | G | 177 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(174): Show | 182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.413+509T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452768 | ||||||
| chr12:51453128
|
T | A | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-411T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51453128 | ||||||
| chr12:51453134
|
G | A | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.414-405G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51453134 | ||||||
| chr12:51453160
|
C | A | 2 | a0001c0001t0002g0063a0001c0001t0002g0067 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.414-379C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51453160 | ||||||
| chr12:51453776
|
C | A | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574+77C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51453776 | ||||||
| chr12:51453870
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0241 | 3 | HG00140.hp2 HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.574+171C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51453870 | ||||||
| chr12:51453924
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.574+225T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51453924 | ||||||
| chr12:51454016
|
C | T | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0186others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.574+317C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454016 | ||||||
| chr12:51454061
|
C | G | 7 | a0001c0001t0004g0021a0001c0001t0004g0028a0001c0001t0004g0042others(4): Show | 7 | HG02027.hp2 HG02040.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.574+362C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454061 | ||||||
| chr12:51454220
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.574+521C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454220 | ||||||
| chr12:51454268
|
G | A | 8 | a0001c0001t0009g0071a0001c0001t0009g0081a0001c0001t0009g0082others(5): Show | 8 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.574+569G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454268 | ||||||
| chr12:51454422
|
T | G | 1 | a0001c0001t0002g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.574+723T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454422 | ||||||
| chr12:51454429
|
G | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.574+730G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454429 | ||||||
| chr12:51454643
|
T | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.574+944T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454643 | ||||||
| chr12:51454837
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.574+1138C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454837 | ||||||
| chr12:51454845
|
G | A | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.574+1146G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454845 | ||||||
| chr12:51454874
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.574+1175C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454874 | ||||||
| chr12:51455061
|
C | T | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.574+1362C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455061 | ||||||
| chr12:51455117
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.574+1418G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455117 | ||||||
| chr12:51455170
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.574+1471A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455170 | ||||||
| chr12:51455271
|
TA | T | 7 | a0001c0001t0001g0260a0001c0001t0001g0273a0001c0001t0003g0328others(4): Show | 7 | HG01074.hp2 HG01515.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.574+1587delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 51455271 | |||||
| chr12:51455324
|
G | A | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.574+1625G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455324 | ||||||
| chr12:51455522
|
A | G | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.574+1823A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455522 | ||||||
| chr12:51455640
|
G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.575-1711G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455640 | ||||||
| chr12:51455687
|
C | T | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.575-1664C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455687 | ||||||
| chr12:51455809
|
C | T | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-1542C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455809 | ||||||
| chr12:51455983
|
C | T | 1 | a0001c0006t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.575-1368C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455983 | ||||||
| chr12:51456026
|
A | G | 1 | a0001c0001t0003g0336 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.575-1325A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456026 | ||||||
| chr12:51456189
|
TGATA | T | 52 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0072others(49): Show | 56 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.575-1155_575-1152d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 51456189 | |||||
| chr12:51456244
|
G | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.575-1107G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456244 | ||||||
| chr12:51456647
|
A | AAGATCAC others(27): Show |
1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.575-696_575-695ins others(34): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 51456647 | |||||
| chr12:51456694
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.575-657T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456694 | ||||||
| chr12:51456833
|
G | A | 2 | a0001c0001t0020g0331a0001c0001t0020g0332 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.575-518G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456833 | ||||||
| chr12:51456900
|
T | A | 2 | a0001c0001t0042g0148a0001c0001t0043g0149 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.575-451T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456900 | ||||||
| chr12:51456943
|
A | G | 180 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0002g0001others(177): Show | 185 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.575-408A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456943 | ||||||
| chr12:51456956
|
A | T | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.575-395A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456956 | ||||||
| chr12:51457064
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.575-287T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457064 | ||||||
| chr12:51457094
|
T | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG00642.hp2 HG01496.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.575-257T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457094 | ||||||
| chr12:51457180
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.575-171G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457180 | ||||||
| chr12:51457342
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.575-9G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457342 | ||||||
| chr12:51457786
|
G | A | 1 | a0001c0001t0002g0005 | 2 | NA18952.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.763+247G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/24 | chr12 | 51457786 | ||||||
| chr12:51457836
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763+297C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/24 | chr12 | 51457836 | ||||||
| chr12:51458366
|
A | C | 1 | a0001c0001t0032g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.764-193A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/24 | chr12 | 51458366 | ||||||
| chr12:51458676
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.855+26T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51458676 | ||||||
| chr12:51458727
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.855+77C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51458727 | ||||||
| chr12:51458949
|
G | GCTCTCCA others(10): Show |
1 | a0001c0014t0003g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.855+303_855+319dup others(17): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr12 | 51458949 | |||||
| chr12:51458977
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.855+327G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51458977 | ||||||
| chr12:51459036
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.855+386A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459036 | ||||||
| chr12:51459260
|
C | T | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.855+610C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459260 | ||||||
| chr12:51459315
|
A | G | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.856-636A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459315 | ||||||
| chr12:51459340
|
G | A | 1 | a0001c0001t0033g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856-611G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459340 | ||||||
| chr12:51459408
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.856-543C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459408 | ||||||
| chr12:51459440
|
A | G | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.856-511A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459440 | ||||||
| chr12:51459739
|
G | A | 2 | a0001c0001t0004g0031a0001c0001t0026g0050 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.856-212G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459739 | ||||||
| chr12:51460142
|
C | T | 27 | a0001c0001t0001g0183a0001c0001t0001g0240a0001c0001t0001g0253others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.1013+34C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460142 | ||||||
| chr12:51460173
|
G | A | 1 | a0005c0012t0001g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1013+65G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460173 | ||||||
| chr12:51460391
|
CT | C | 309 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(306): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1013+289delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 51460391 | |||||
| chr12:51460719
|
C | T | 1 | a0001c0002t0044g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1014-485C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460719 | ||||||
| chr12:51460720
|
G | A | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1014-484G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460720 | ||||||
| chr12:51460794
|
T | C | 8 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 8 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014-410T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460794 | ||||||
| chr12:51461046
|
C | G | 1 | a0001c0006t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1014-158C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461046 | ||||||
| chr12:51461074
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1014-130T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461074 | ||||||
| chr12:51461105
|
A | G | 1 | a0001c0001t0015g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1014-99A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461105 | ||||||
| chr12:51461111
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1014-93G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461111 | ||||||
| chr12:51461113
|
T | C | 1 | a0001c0001t0004g0027 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1014-91T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461113 | ||||||
| chr12:51461302
|
C | G | 1 | a0001c0001t0004g0055 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1101+11C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461302 | ||||||
| chr12:51461476
|
C | T | 1 | a0001c0001t0003g0308 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1101+185C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461476 | ||||||
| chr12:51461631
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1101+340A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461631 | ||||||
| chr12:51461719
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1101+428T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461719 | ||||||
| chr12:51461846
|
C | T | 3 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151 | 3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102-464C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461846 | ||||||
| chr12:51461884
|
TTTGA | T | 43 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0027others(40): Show | 43 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1102-421_1102-418d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 51461884 | |||||
| chr12:51461943
|
A | G | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1102-367A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461943 | ||||||
| chr12:51461990
|
T | TA | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1102-316dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 51461990 | |||||
| chr12:51462072
|
T | G | 2 | a0001c0001t0020g0331a0001c0001t0020g0332 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1102-238T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51462072 | ||||||
| chr12:51462144
|
A | C | 1 | a0001c0001t0048g0022 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1102-166A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51462144 | ||||||
| chr12:51462200
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1102-110G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51462200 | ||||||
| chr12:51462486
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1248+30A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462486 | ||||||
| chr12:51462538
|
A | G | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+82A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462538 | ||||||
| chr12:51462695
|
C | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1248+239C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462695 | ||||||
| chr12:51462807
|
C | T | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1248+351C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462807 | ||||||
| chr12:51462851
|
T | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1248+395T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462851 | ||||||
| chr12:51462892
|
C | CA | 10 | a0001c0001t0001g0187a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG01891.hp1 HG02080.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+453dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51462892 | |||||
| chr12:51462892
|
C | CAA | 169 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(166): Show | 174 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1248+452_1248+453d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51462892 | |||||
| chr12:51462966
|
G | A | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+510G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462966 | ||||||
| chr12:51463042
|
T | C | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1249-572T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463042 | ||||||
| chr12:51463076
|
G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1249-538G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463076 | ||||||
| chr12:51463110
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1249-504T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463110 | ||||||
| chr12:51463409
|
G | C | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-205G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463409 | ||||||
| chr12:51463410
|
G | GGT | 38 | a0001c0001t0001g0213a0001c0001t0001g0225a0001c0001t0001g0281others(35): Show | 40 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1249-165_1249-164d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | |||||
| chr12:51463410
|
G | GGTGT | 12 | a0001c0001t0001g0215a0001c0001t0001g0247a0001c0001t0001g0267others(9): Show | 13 | HG01433.hp1 HG01515.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1249-167_1249-164d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | |||||
| chr12:51463410
|
GGT | G | 57 | a0001c0001t0001g0195a0001c0001t0001g0242a0001c0001t0001g0251others(54): Show | 57 | HG00438.hp1 HG00673.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1249-165_1249-164d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | |||||
| chr12:51463410
|
GGTGT | G | 104 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(101): Show | 109 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1249-167_1249-164d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | |||||
| chr12:51463410
|
GGTGTGT | G | 7 | a0001c0001t0002g0117a0001c0001t0004g0020a0001c0001t0004g0046others(4): Show | 7 | HG01099.hp2 HG01167.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1249-169_1249-164d others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | |||||
| chr12:51463410
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0003g0326 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1249-175_1249-164d others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | |||||
| chr12:51463412
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1249-202T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463412 | ||||||
| chr12:51463480
|
C | T | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-134C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463480 | ||||||
| chr12:51463577
|
T | A | 1 | a0001c0001t0049g0033 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1249-37T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463577 | ||||||
| chr12:51463805
|
C | T | 2 | a0001c0001t0042g0148a0001c0001t0043g0149 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1349+91C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51463805 | ||||||
| chr12:51464064
|
C | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1349+350C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464064 | ||||||
| chr12:51464117
|
AC | A | 181 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0002g0001others(178): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1349+406delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51464117 | |||||
| chr12:51464214
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1349+500G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464214 | ||||||
| chr12:51464530
|
T | G | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1349+816T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464530 | ||||||
| chr12:51464573
|
G | A | 1 | a0001c0001t0004g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1349+859G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464573 | ||||||
| chr12:51464793
|
G | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1349+1079G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464793 | ||||||
| chr12:51464835
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1349+1121A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464835 | ||||||
| chr12:51465057
|
T | C | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1349+1343T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465057 | ||||||
| chr12:51465513
|
G | T | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1349+1799G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465513 | ||||||
| chr12:51465524
|
T | C | 2 | a0001c0001t0020g0331a0001c0001t0020g0332 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1349+1810T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465524 | ||||||
| chr12:51465534
|
C | G | 1 | a0001c0002t0005g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1349+1820C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465534 | ||||||
| chr12:51465539
|
C | T | 1 | a0001c0002t0005g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1349+1825C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465539 | ||||||
| chr12:51465825
|
C | A | 1 | a0001c0001t0008g0262 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1349+2111C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465825 | ||||||
| chr12:51465910
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1349+2196C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465910 | ||||||
| chr12:51466059
|
T | G | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1349+2345T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466059 | ||||||
| chr12:51466166
|
G | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1349+2452G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466166 | ||||||
| chr12:51466240
|
C | T | 1 | a0001c0001t0002g0005 | 2 | NA18952.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1349+2526C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466240 | ||||||
| chr12:51466535
|
CTTAAA | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(83): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1349+2827_1349+283 others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51466535 | |||||
| chr12:51466595
|
A | C | 1 | a0001c0002t0005g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1349+2881A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466595 | ||||||
| chr12:51466695
|
A | T | 46 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1350-2919A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466695 | ||||||
| chr12:51466729
|
A | G | 1 | a0001c0001t0025g0023 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1350-2885A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466729 | ||||||
| chr12:51466806
|
A | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1350-2808A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466806 | ||||||
| chr12:51466943
|
ATG | A | 302 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(299): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1350-2647_1350-264 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51466943 | |||||
| chr12:51467070
|
C | T | 2 | a0001c0002t0005g0166a0001c0011t0047g0167 | 2 | NA18979.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1350-2544C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467070 | ||||||
| chr12:51467079
|
A | C | 1 | a0001c0001t0003g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1350-2535A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467079 | ||||||
| chr12:51467638
|
T | G | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0137others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350-1976T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467638 | ||||||
| chr12:51467666
|
A | G | 8 | a0001c0001t0002g0072a0001c0001t0002g0086a0001c0001t0002g0087others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1350-1948A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467666 | ||||||
| chr12:51467771
|
CTTAAT | C | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1840_1350-183 others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51467771 | |||||
| chr12:51467864
|
A | C | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1350-1750A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467864 | ||||||
| chr12:51468302
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1350-1312T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468302 | ||||||
| chr12:51468321
|
C | T | 7 | a0001c0001t0001g0183a0001c0001t0001g0240a0001c0001t0001g0267others(4): Show | 7 | HG01081.hp2 HG01255.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350-1293C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468321 | ||||||
| chr12:51468333
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1350-1281C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468333 | ||||||
| chr12:51468425
|
C | G | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1350-1189C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468425 | ||||||
| chr12:51468530
|
C | T | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1350-1084C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468530 | ||||||
| chr12:51468539
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1350-1075C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468539 | ||||||
| chr12:51468754
|
C | T | 1 | a0001c0001t0004g0039 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1350-860C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468754 | ||||||
| chr12:51468865
|
C | G | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0137others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350-749C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468865 | ||||||
| chr12:51468874
|
C | G | 4 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-740C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468874 | ||||||
| chr12:51468876
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1350-738C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468876 | ||||||
| chr12:51469174
|
C | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1350-440C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51469174 | ||||||
| chr12:51469544
|
A | G | 8 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 8 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1350-70A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51469544 | ||||||
| chr12:51469553
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1350-61T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51469553 | ||||||
| chr12:51469859
|
T | C | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1524+71T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 12/24 | chr12 | 51469859 | ||||||
| chr12:51470680
|
C | T | 2 | a0001c0001t0020g0331a0001c0001t0020g0332 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1658+155C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470680 | ||||||
| chr12:51470848
|
C | T | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1658+323C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470848 | ||||||
| chr12:51470864
|
T | G | 1 | a0001c0001t0001g0292 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1658+339T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470864 | ||||||
| chr12:51470874
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1658+349G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470874 | ||||||
| chr12:51470879
|
G | GT | 88 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(85): Show | 92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1658+361dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 51470879 | |||||
| chr12:51470957
|
T | C | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1659-330T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470957 | ||||||
| chr12:51471098
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1659-189G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471098 | ||||||
| chr12:51471153
|
G | C | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1659-134G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471153 | ||||||
| chr12:51471184
|
G | A | 5 | a0001c0001t0003g0009a0001c0001t0003g0300a0001c0001t0003g0302others(2): Show | 6 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1659-103G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471184 | ||||||
| chr12:51471195
|
T | C | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1659-92T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471195 | ||||||
| chr12:51471255
|
A | G | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1659-32A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471255 | ||||||
| chr12:51471259
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1659-28G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471259 | ||||||
| chr12:51471651
|
A | G | 1 | a0001c0001t0003g0319 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1904+119A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51471651 | ||||||
| chr12:51471831
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1904+299A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51471831 | ||||||
| chr12:51472038
|
A | G | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1904+506A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472038 | ||||||
| chr12:51472076
|
C | T | 4 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1904+544C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472076 | ||||||
| chr12:51472169
|
C | T | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1904+637C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472169 | ||||||
| chr12:51472319
|
C | T | 8 | a0001c0001t0002g0072a0001c0001t0002g0086a0001c0001t0002g0087others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904+787C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472319 | ||||||
| chr12:51472361
|
A | T | 1 | a0001c0001t0004g0038 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1904+829A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472361 | ||||||
| chr12:51472605
|
A | G | 1 | a0001c0001t0003g0304 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1904+1073A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472605 | ||||||
| chr12:51472621
|
C | T | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1904+1089C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472621 | ||||||
| chr12:51472622
|
A | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1904+1090A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472622 | ||||||
| chr12:51472640
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1904+1108G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472640 | ||||||
| chr12:51472880
|
A | T | 1 | a0001c0003t0005g0006 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1904+1348A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472880 | ||||||
| chr12:51472911
|
T | A | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1904+1379T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472911 | ||||||
| chr12:51472977
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1905-1365C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472977 | ||||||
| chr12:51472991
|
A | G | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1905-1351A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472991 | ||||||
| chr12:51473050
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1905-1292C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473050 | ||||||
| chr12:51473114
|
GATTTTGA others(19): Show |
G | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1905-1225_1905-120 others(30): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 51473114 | |||||
| chr12:51473158
|
C | T | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1905-1184C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473158 | ||||||
| chr12:51473275
|
A | G | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1905-1067A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473275 | ||||||
| chr12:51473329
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1905-1013C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473329 | ||||||
| chr12:51473700
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0290 | 2 | HG01346.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1905-642A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473700 | ||||||
| chr12:51473852
|
A | G | 1 | a0001c0001t0014g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1905-490A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473852 | ||||||
| chr12:51474027
|
A | AAAAC | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1905-312_1905-311i others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 51474027 | |||||
| chr12:51474327
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1905-15A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51474327 | ||||||
| chr12:51475237
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2172+31G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475237 | ||||||
| chr12:51475314
|
G | A | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.2172+108G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475314 | ||||||
| chr12:51475618
|
G | A | 1 | a0001c0001t0035g0218 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2172+412G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475618 | ||||||
| chr12:51475748
|
T | C | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2172+542T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475748 | ||||||
| chr12:51476070
|
C | T | 1 | a0001c0002t0005g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2172+864C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476070 | ||||||
| chr12:51476164
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2172+958A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476164 | ||||||
| chr12:51476202
|
C | T | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2172+996C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476202 | ||||||
| chr12:51476231
|
C | T | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2172+1025C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476231 | ||||||
| chr12:51476459
|
C | T | 1 | a0006c0015t0001g0338 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2172+1253C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476459 | ||||||
| chr12:51476490
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2172+1284A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476490 | ||||||
| chr12:51476536
|
A | G | 2 | a0001c0001t0014g0015a0001c0001t0014g0016 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2172+1330A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476536 | ||||||
| chr12:51476602
|
G | T | 10 | a0001c0001t0002g0072a0001c0001t0002g0086a0001c0001t0002g0087others(7): Show | 10 | HG00733.hp1 HG00735.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.2172+1396G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476602 | ||||||
| chr12:51476640
|
G | A | 1 | a0001c0001t0016g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2172+1434G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476640 | ||||||
| chr12:51476901
|
CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2172+1700_2172+171 others(15): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51476901 | |||||
| chr12:51476906
|
CT | C | 143 | a0001c0001t0001g0194a0001c0001t0002g0001a0001c0001t0002g0004others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.2172+1717delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51476906 | |||||
| chr12:51477001
|
G | A | 21 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(18): Show | 21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.2172+1795G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477001 | ||||||
| chr12:51477345
|
G | C | 1 | a0001c0001t0002g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2172+2139G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477345 | ||||||
| chr12:51477348
|
T | TGGTATTA others(4): Show |
1 | a0001c0001t0017g0255 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2172+2143_2172+215 others(15): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51477348 | |||||
| chr12:51477578
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2172+2372C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477578 | ||||||
| chr12:51477665
|
T | A | 1 | a0003c0007t0003g0310 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2172+2459T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477665 | ||||||
| chr12:51477788
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0224a0001c0001t0001g0232others(2): Show | 5 | HG00099.hp1 HG01433.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172+2582C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477788 | ||||||
| chr12:51477845
|
A | G | 183 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(180): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.2172+2639A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477845 | ||||||
| chr12:51477851
|
A | G | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2172+2645A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477851 | ||||||
| chr12:51477913
|
C | T | 1 | a0001c0001t0023g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2172+2707C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477913 | ||||||
| chr12:51477914
|
G | A | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2172+2708G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477914 | ||||||
| chr12:51478071
|
C | T | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2172+2865C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478071 | ||||||
| chr12:51478098
|
AC | A | 4 | a0001c0003t0005g0006a0001c0003t0005g0180a0001c0003t0005g0181others(1): Show | 5 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172+2895delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478098 | |||||
| chr12:51478154
|
A | G | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2172+2948A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478154 | ||||||
| chr12:51478274
|
C | CA | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 149 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2172+3083dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478274 | |||||
| chr12:51478274
|
C | CAA | 31 | a0001c0001t0002g0089a0001c0001t0002g0108a0001c0001t0004g0029others(28): Show | 31 | HG00558.hp2 HG01258.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.2172+3082_2172+308 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478274 | |||||
| chr12:51478438
|
T | TA | 12 | a0001c0001t0001g0287a0001c0001t0021g0155a0001c0001t0021g0156others(9): Show | 13 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2172+3244dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478438 | |||||
| chr12:51478453
|
A | T | 183 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(180): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.2172+3247A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478453 | ||||||
| chr12:51478492
|
A | G | 178 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.2172+3286A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478492 | ||||||
| chr12:51478517
|
G | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0202a0001c0001t0001g0207others(2): Show | 5 | NA18988.hp1 NA19003.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.2172+3311G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478517 | ||||||
| chr12:51478646
|
C | T | 183 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(180): Show | 188 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.2172+3440C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478646 | ||||||
| chr12:51478761
|
C | T | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2172+3555C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478761 | ||||||
| chr12:51478795
|
A | G | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.2172+3589A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478795 | ||||||
| chr12:51478939
|
G | GCCTCA | 311 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(308): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2172+3734_2172+373 others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478939 | |||||
| chr12:51479103
|
T | C | 1 | a0001c0001t0035g0218 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2172+3897T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479103 | ||||||
| chr12:51479256
|
T | C | 1 | a0001c0001t0002g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2172+4050T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479256 | ||||||
| chr12:51479325
|
T | C | 1 | a0001c0001t0002g0106 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2172+4119T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479325 | ||||||
| chr12:51479374
|
T | C | 1 | a0001c0002t0005g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2172+4168T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479374 | ||||||
| chr12:51479410
|
T | G | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2172+4204T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479410 | ||||||
| chr12:51479441
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2172+4235C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479441 | ||||||
| chr12:51479512
|
C | T | 1 | a0001c0001t0016g0344 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2172+4306C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479512 | ||||||
| chr12:51479530
|
T | TA | 3 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151 | 3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2172+4325dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479530 | |||||
| chr12:51479698
|
AAG | A | 131 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(128): Show | 135 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2172+4494_2172+449 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479698 | |||||
| chr12:51479699
|
AG | A | 46 | a0001c0001t0002g0063a0001c0001t0002g0086a0001c0001t0004g0030others(43): Show | 47 | HG00558.hp2 HG00735.hp2 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.2172+4494delG | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479699 | ||||||
| chr12:51479700
|
G | A | 3 | a0001c0001t0021g0156a0001c0001t0037g0346a0001c0002t0010g0019 | 3 | HG01884.hp1 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2172+4494G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479700 | ||||||
| chr12:51479784
|
A | G | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2172+4578A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479784 | ||||||
| chr12:51479822
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2172+4616T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479822 | ||||||
| chr12:51479969
|
AT | A | 161 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2172+4782delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479969 | |||||
| chr12:51479969
|
ATT | A | 140 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(137): Show | 144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2172+4781_2172+478 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479969 | |||||
| chr12:51480066
|
G | A | 2 | a0001c0001t0024g0110a0001c0001t0024g0118 | 2 | NA18981.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2172+4860G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480066 | ||||||
| chr12:51480071
|
G | A | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2172+4865G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480071 | ||||||
| chr12:51480122
|
G | A | 1 | a0001c0001t0040g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2172+4916G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480122 | ||||||
| chr12:51480130
|
G | A | 3 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151 | 3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2172+4924G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480130 | ||||||
| chr12:51480190
|
C | T | 1 | a0001c0001t0025g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2172+4984C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480190 | ||||||
| chr12:51480270
|
C | T | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0072others(56): Show | 62 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2172+5064C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480270 | ||||||
| chr12:51480276
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2172+5070C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480276 | ||||||
| chr12:51480326
|
T | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0213 | 2 | NA18946.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2172+5120T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480326 | ||||||
| chr12:51480369
|
G | A | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2172+5163G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480369 | ||||||
| chr12:51480372
|
G | T | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2172+5166G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480372 | ||||||
| chr12:51480395
|
G | A | 6 | a0001c0001t0009g0071a0001c0001t0009g0081a0001c0001t0009g0082others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2172+5189G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480395 | ||||||
| chr12:51480431
|
G | A | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2172+5225G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480431 | ||||||
| chr12:51480612
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2173-5175G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480612 | ||||||
| chr12:51480889
|
G | A | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2173-4898G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480889 | ||||||
| chr12:51480890
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2173-4897C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480890 | ||||||
| chr12:51481341
|
C | T | 1 | a0001c0001t0003g0330 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2173-4446C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481341 | ||||||
| chr12:51481463
|
G | A | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2173-4324G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481463 | ||||||
| chr12:51481484
|
A | G | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2173-4303A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481484 | ||||||
| chr12:51481506
|
C | G | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-4281C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481506 | ||||||
| chr12:51481512
|
G | A | 2 | a0001c0001t0042g0148a0001c0001t0043g0149 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2173-4275G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481512 | ||||||
| chr12:51481620
|
T | C | 1 | a0001c0001t0026g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2173-4167T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481620 | ||||||
| chr12:51481654
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2173-4133G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481654 | ||||||
| chr12:51481722
|
C | T | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2173-4065C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481722 | ||||||
| chr12:51481729
|
G | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(141): Show | 148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.2173-4058G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481729 | ||||||
| chr12:51481790
|
T | TA | 8 | a0001c0001t0001g0204a0001c0001t0009g0071a0001c0001t0009g0081others(5): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2173-3985dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51481790 | |||||
| chr12:51481792
|
A | T | 1 | a0001c0001t0003g0319 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2173-3995A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481792 | ||||||
| chr12:51481815
|
G | A | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-3972G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481815 | ||||||
| chr12:51481916
|
C | T | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2173-3871C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481916 | ||||||
| chr12:51482091
|
A | G | 1 | a0001c0001t0016g0343 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2173-3696A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482091 | ||||||
| chr12:51482185
|
C | G | 1 | a0001c0001t0003g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2173-3602C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482185 | ||||||
| chr12:51482217
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2173-3570T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482217 | ||||||
| chr12:51482746
|
C | A | 1 | a0001c0001t0017g0255 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2173-3041C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482746 | ||||||
| chr12:51482824
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2173-2963A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482824 | ||||||
| chr12:51482848
|
A | C | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2173-2939A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482848 | ||||||
| chr12:51482873
|
A | T | 1 | a0001c0001t0017g0255 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2173-2914A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482873 | ||||||
| chr12:51483035
|
C | T | 50 | a0001c0001t0002g0102a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2173-2752C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483035 | ||||||
| chr12:51483058
|
C | G | 1 | a0001c0001t0004g0037 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2173-2729C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483058 | ||||||
| chr12:51483232
|
C | T | 1 | a0001c0001t0003g0329 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2173-2555C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483232 | ||||||
| chr12:51483354
|
C | CA | 148 | a0001c0001t0001g0187a0001c0001t0001g0208a0001c0001t0001g0213others(145): Show | 155 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.2173-2421dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483354 | |||||
| chr12:51483354
|
C | CAA | 11 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(8): Show | 11 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.2173-2422_2173-242 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483354 | |||||
| chr12:51483354
|
CA | C | 7 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173-2421delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483354 | |||||
| chr12:51483356
|
A | C | 3 | a0001c0001t0001g0290a0001c0001t0020g0331a0001c0001t0020g0332 | 3 | HG01346.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2173-2431A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483356 | ||||||
| chr12:51483470
|
C | T | 160 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(157): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2173-2317C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483470 | ||||||
| chr12:51483472
|
C | CT | 7 | a0001c0001t0009g0071a0001c0001t0009g0081a0001c0001t0009g0082others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173-2304dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483472 | |||||
| chr12:51483552
|
A | G | 208 | a0001c0001t0001g0234a0001c0001t0002g0001a0001c0001t0002g0004others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2173-2235A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483552 | ||||||
| chr12:51483612
|
A | AT | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2173-2167dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483612 | |||||
| chr12:51483696
|
T | G | 1 | a0001c0001t0050g0040 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2173-2091T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483696 | ||||||
| chr12:51483721
|
G | A | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2173-2066G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483721 | ||||||
| chr12:51483740
|
CT | C | 13 | a0001c0001t0001g0219a0001c0001t0003g0002a0001c0001t0003g0301others(10): Show | 15 | HG00673.hp1 HG00735.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.2173-2037delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483740 | |||||
| chr12:51483859
|
G | C | 1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2173-1928G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483859 | ||||||
| chr12:51483883
|
C | T | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-1904C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483883 | ||||||
| chr12:51483985
|
G | A | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-1802G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483985 | ||||||
| chr12:51483994
|
T | G | 1 | a0001c0001t0017g0255 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2173-1793T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483994 | ||||||
| chr12:51484071
|
T | A | 1 | a0001c0001t0006g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2173-1716T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484071 | ||||||
| chr12:51484117
|
G | GGGA | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-1666_2173-166 others(7): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51484117 | |||||
| chr12:51484211
|
G | T | 23 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0301others(20): Show | 25 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2173-1576G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484211 | ||||||
| chr12:51484391
|
A | G | 180 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(177): Show | 185 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.2173-1396A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484391 | ||||||
| chr12:51484654
|
GCTCTCA | G | 5 | a0001c0001t0001g0184a0001c0001t0001g0250a0001c0001t0001g0251others(2): Show | 5 | HG02109.hp2 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-1128_2173-112 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51484654 | |||||
| chr12:51484686
|
A | C | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173-1101A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484686 | ||||||
| chr12:51484888
|
A | C | 147 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(144): Show | 152 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.2173-899A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484888 | ||||||
| chr12:51484915
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2173-872G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484915 | ||||||
| chr12:51484976
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2173-811G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484976 | ||||||
| chr12:51485047
|
A | G | 147 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(144): Show | 152 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.2173-740A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485047 | ||||||
| chr12:51485133
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2173-654C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485133 | ||||||
| chr12:51485146
|
G | A | 24 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(21): Show | 24 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.2173-641G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485146 | ||||||
| chr12:51485410
|
T | C | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-377T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485410 | ||||||
| chr12:51485477
|
T | C | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173-310T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485477 | ||||||
| chr12:51485617
|
T | A | 1 | a0001c0002t0005g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2173-170T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485617 | ||||||
| chr12:51486042
|
G | T | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2286+142G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486042 | ||||||
| chr12:51486309
|
A | G | 32 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0111others(29): Show | 34 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2286+409A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486309 | ||||||
| chr12:51486314
|
T | G | 5 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2286+414T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486314 | ||||||
| chr12:51486326
|
C | G | 8 | a0001c0001t0023g0147a0001c0001t0040g0145a0001c0003t0005g0006others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2286+426C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486326 | ||||||
| chr12:51486424
|
C | T | 2 | a0001c0002t0010g0150a0001c0002t0010g0151 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2286+524C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486424 | ||||||
| chr12:51486485
|
G | A | 147 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(144): Show | 152 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.2286+585G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486485 | ||||||
| chr12:51486588
|
A | G | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2286+688A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486588 | ||||||
| chr12:51486628
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2286+728G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486628 | ||||||
| chr12:51486646
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2286+746C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486646 | ||||||
| chr12:51486661
|
T | A | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2286+761T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486661 | ||||||
| chr12:51486739
|
C | T | 175 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(172): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.2286+839C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486739 | ||||||
| chr12:51486786
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2286+886C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486786 | ||||||
| chr12:51486913
|
C | T | 1 | a0001c0001t0043g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2286+1013C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486913 | ||||||
| chr12:51487043
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0072others(48): Show | 55 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2286+1143C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487043 | ||||||
| chr12:51487044
|
G | A | 1 | a0001c0002t0010g0019 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2286+1144G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487044 | ||||||
| chr12:51487193
|
C | T | 1 | a0001c0001t0004g0032 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2286+1293C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487193 | ||||||
| chr12:51487338
|
G | A | 3 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151 | 3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2287-1361G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487338 | ||||||
| chr12:51487512
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2287-1187G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487512 | ||||||
| chr12:51487513
|
C | A | 1 | a0001c0001t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2287-1186C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487513 | ||||||
| chr12:51487598
|
A | G | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2287-1101A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487598 | ||||||
| chr12:51487884
|
C | T | 1 | a0001c0001t0042g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2287-815C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487884 | ||||||
| chr12:51487941
|
T | C | 175 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(172): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.2287-758T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487941 | ||||||
| chr12:51488028
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2287-671A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488028 | ||||||
| chr12:51488139
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2287-560C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488139 | ||||||
| chr12:51488469
|
G | A | 46 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2287-230G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488469 | ||||||
| chr12:51488571
|
CT | C | 174 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0268others(171): Show | 179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.2287-112delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 51488571 | |||||
| chr12:51488571
|
CTT | C | 8 | a0001c0001t0004g0020a0001c0001t0004g0060a0001c0001t0015g0075others(5): Show | 8 | HG00609.hp1 HG01167.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2287-113_2287-112d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 51488571 | |||||
| chr12:51488644
|
T | C | 1 | a0001c0001t0009g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2287-55T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488644 | ||||||
| chr12:51489002
|
G | T | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2448+142G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489002 | ||||||
| chr12:51489006
|
T | G | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2448+146T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489006 | ||||||
| chr12:51489302
|
A | G | 9 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(6): Show | 9 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2449-398A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489302 | ||||||
| chr12:51489354
|
C | A | 2 | a0001c0001t0004g0037a0001c0001t0004g0061 | 2 | HG00673.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.2449-346C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489354 | ||||||
| chr12:51489408
|
T | C | 4 | a0001c0001t0004g0030a0001c0001t0004g0038a0001c0001t0004g0049others(1): Show | 4 | NA18989.hp1 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2449-292T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489408 | ||||||
| chr12:51489461
|
G | A | 1 | a0001c0001t0004g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2449-239G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489461 | ||||||
| chr12:51489518
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2449-182C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489518 | ||||||
| chr12:51490270
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2700+319T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490270 | ||||||
| chr12:51490345
|
G | A | 1 | a0001c0001t0023g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2700+394G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490345 | ||||||
| chr12:51490415
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2700+464C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490415 | ||||||
| chr12:51490433
|
C | G | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2700+482C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490433 | ||||||
| chr12:51490513
|
A | G | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2700+562A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490513 | ||||||
| chr12:51490549
|
C | G | 1 | a0001c0001t0007g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2700+598C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490549 | ||||||
| chr12:51490562
|
C | CA | 21 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0236others(18): Show | 21 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2700+633dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51490562 | |||||
| chr12:51490562
|
CA | C | 10 | a0001c0001t0001g0257a0001c0001t0002g0138a0001c0001t0002g0139others(7): Show | 10 | HG00597.hp1 HG01346.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.2700+633delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51490562 | |||||
| chr12:51490586
|
A | G | 1 | a0001c0001t0011g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2700+635A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490586 | ||||||
| chr12:51490587
|
T | TGAGGTGG | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(66): Show | 71 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2700+637_2700+643d others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51490587 | |||||
| chr12:51490655
|
G | T | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2700+704G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490655 | ||||||
| chr12:51490676
|
A | G | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2700+725A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490676 | ||||||
| chr12:51490858
|
A | G | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2700+907A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490858 | ||||||
| chr12:51490869
|
T | G | 1 | a0001c0001t0034g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2700+918T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490869 | ||||||
| chr12:51490886
|
T | G | 1 | a0001c0001t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2700+935T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490886 | ||||||
| chr12:51491015
|
A | G | 28 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(25): Show | 28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.2700+1064A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491015 | ||||||
| chr12:51491034
|
A | G | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2700+1083A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491034 | ||||||
| chr12:51491037
|
G | A | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2700+1086G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491037 | ||||||
| chr12:51491059
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2700+1108G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491059 | ||||||
| chr12:51491098
|
A | G | 1 | a0005c0012t0001g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2700+1147A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491098 | ||||||
| chr12:51491102
|
T | C | 1 | a0001c0001t0043g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2700+1151T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491102 | ||||||
| chr12:51491204
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2700+1253G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491204 | ||||||
| chr12:51491233
|
A | T | 1 | a0001c0006t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2700+1282A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491233 | ||||||
| chr12:51491346
|
G | A | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2700+1395G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491346 | ||||||
| chr12:51491643
|
T | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0273 | 2 | HG01074.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2700+1692T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491643 | ||||||
| chr12:51491697
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2700+1746C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491697 | ||||||
| chr12:51491737
|
G | GCA | 65 | a0001c0001t0002g0004a0001c0001t0002g0064a0001c0001t0002g0073others(62): Show | 66 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2700+1787_2700+178 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | |||||
| chr12:51491737
|
G | GCACA | 18 | a0001c0001t0002g0005a0001c0001t0002g0089a0001c0001t0002g0096others(15): Show | 19 | HG00544.hp2 HG00741.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | |||||
| chr12:51491737
|
G | GCACACA | 3 | a0001c0001t0002g0076a0001c0001t0004g0024a0001c0001t0014g0103 | 3 | HG01978.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | |||||
| chr12:51491737
|
G | GCACACAC others(1): Show |
7 | a0001c0001t0004g0021a0001c0001t0004g0038a0001c0001t0004g0043others(4): Show | 7 | HG02040.hp2 HG02818.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | |||||
| chr12:51491737
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0058 | 3 | HG02027.hp2 NA18946.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | |||||
| chr12:51491737
|
GCAGACAC others(3): Show |
G | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0134 | 3 | HG00639.hp1 HG03490.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2700+1789_2700+179 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | |||||
| chr12:51491738
|
CAG | C | 7 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0009g0071others(4): Show | 7 | HG00733.hp1 HG00735.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2700+1789_2700+179 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491738 | |||||
| chr12:51491740
|
G | C | 131 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(128): Show | 135 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2700+1789G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491740 | ||||||
| chr12:51491740
|
G | GAC | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(97): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.2700+1826_2700+182 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACAC | 15 | a0001c0001t0001g0195a0001c0001t0001g0209a0001c0001t0001g0228others(12): Show | 15 | HG00544.hp1 HG01255.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.2700+1824_2700+182 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACAC | 7 | a0001c0001t0001g0200a0001c0001t0001g0280a0001c0001t0001g0287others(4): Show | 7 | HG01346.hp1 HG04184.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.2700+1822_2700+182 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(1): Show |
7 | a0001c0001t0001g0247a0001c0001t0022g0154a0001c0001t0037g0346others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2700+1820_2700+182 others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(3): Show |
9 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(6): Show | 10 | HG02055.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2700+1818_2700+182 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(5): Show |
2 | a0001c0002t0010g0019a0001c0005t0005g0160 | 2 | HG01884.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.2700+1816_2700+182 others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(7): Show |
4 | a0001c0002t0005g0163a0001c0002t0005g0164a0001c0002t0005g0173others(1): Show | 4 | HG00558.hp2 NA18941.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2700+1814_2700+182 others(18): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(9): Show |
6 | a0001c0002t0005g0162a0001c0002t0005g0165a0001c0002t0005g0166others(3): Show | 6 | HG02109.hp1 NA18979.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.2700+1812_2700+182 others(20): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(11): Show |
5 | a0001c0002t0005g0158a0001c0002t0005g0159a0001c0002t0005g0161others(2): Show | 5 | HG01891.hp1 HG02071.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2700+1810_2700+182 others(22): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491740
|
G | GACACACA others(13): Show |
2 | a0001c0002t0005g0169a0001c0002t0005g0175 | 2 | NA18962.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2700+1808_2700+182 others(24): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | |||||
| chr12:51491778
|
C | CACA | 11 | a0001c0001t0001g0186a0001c0001t0001g0232a0001c0001t0001g0276others(8): Show | 11 | HG01243.hp2 HG01496.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.2700+1827_2700+182 others(7): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | ||||||
| chr12:51491778
|
C | CACACACA others(4): Show |
1 | a0001c0003t0046g0182 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2700+1827_2700+182 others(15): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | ||||||
| chr12:51491778
|
C | CACACACA others(6): Show |
1 | a0001c0002t0005g0176 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2700+1827_2700+182 others(17): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | ||||||
| chr12:51491778
|
C | CACACACA others(10): Show |
1 | a0001c0002t0005g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2700+1827_2700+182 others(21): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | ||||||
| chr12:51491939
|
A | G | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2701-1765A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491939 | ||||||
| chr12:51492086
|
G | T | 4 | a0001c0001t0003g0301a0001c0001t0003g0316a0001c0001t0003g0318others(1): Show | 4 | HG00673.hp1 NA19003.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2701-1618G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492086 | ||||||
| chr12:51492426
|
A | G | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2701-1278A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492426 | ||||||
| chr12:51492523
|
C | T | 3 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151 | 3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2701-1181C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492523 | ||||||
| chr12:51492712
|
G | T | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2701-992G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492712 | ||||||
| chr12:51492738
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2701-966A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492738 | ||||||
| chr12:51492775
|
A | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0080a0001c0001t0002g0089others(11): Show | 14 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.2701-929A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492775 | ||||||
| chr12:51493034
|
A | T | 46 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2701-670A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493034 | ||||||
| chr12:51493086
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0225a0001c0001t0001g0243 | 3 | HG00438.hp2 HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2701-618G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493086 | ||||||
| chr12:51493094
|
T | C | 1 | a0001c0008t0036g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2701-610T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493094 | ||||||
| chr12:51493381
|
C | T | 1 | a0001c0001t0037g0346 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2701-323C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493381 | ||||||
| chr12:51493384
|
T | TTG | 9 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2701-300_2701-299d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51493384 | |||||
| chr12:51493384
|
T | TTGTG | 3 | a0001c0001t0016g0034a0001c0001t0016g0343a0001c0001t0016g0344 | 3 | NA18943.hp2 NA18963.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2701-302_2701-299d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51493384 | |||||
| chr12:51493543
|
T | C | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0025g0026 | 3 | HG01891.hp2 HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2701-161T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493543 | ||||||
| chr12:51493576
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2701-128C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493576 | ||||||
| chr12:51493883
|
T | C | 3 | a0001c0001t0002g0073a0001c0001t0002g0116a0001c0001t0002g0124 | 3 | HG01993.hp2 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2769+111T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493883 | ||||||
| chr12:51493927
|
T | C | 3 | a0001c0002t0005g0171a0001c0002t0005g0173a0001c0002t0045g0172 | 3 | NA18955.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2769+155T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493927 | ||||||
| chr12:51493944
|
A | G | 21 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(18): Show | 21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.2769+172A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493944 | ||||||
| chr12:51493945
|
T | C | 1 | a0001c0001t0031g0264 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2769+173T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493945 | ||||||
| chr12:51494401
|
ATTCTTTT others(2): Show |
A | 3 | a0001c0002t0027g0297a0001c0002t0027g0298a0001c0002t0044g0299 | 3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2770-532_2770-524d others(11): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 51494401 | |||||
| chr12:51494413
|
CT | C | 141 | a0001c0001t0001g0196a0001c0001t0002g0001a0001c0001t0002g0004others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2770-517delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 51494413 | |||||
| chr12:51494503
|
C | T | 1 | a0001c0001t0003g0330 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2770-442C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494503 | ||||||
| chr12:51494571
|
T | G | 1 | a0001c0001t0053g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2770-374T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494571 | ||||||
| chr12:51494671
|
C | T | 1 | a0001c0001t0015g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2770-274C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494671 | ||||||
| chr12:51494702
|
T | C | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2770-243T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494702 | ||||||
| chr12:51494823
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2770-122G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494823 | ||||||
| chr12:51495214
|
G | T | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2943+96G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495214 | ||||||
| chr12:51495470
|
C | CT | 49 | a0001c0001t0002g0076a0001c0001t0002g0091a0001c0001t0002g0125others(46): Show | 49 | HG00438.hp1 HG00544.hp2 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.2943+374dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | |||||
| chr12:51495470
|
C | CTT | 77 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(74): Show | 81 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2943+373_2943+374d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | |||||
| chr12:51495470
|
C | CTTT | 12 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0089others(9): Show | 12 | HG01169.hp2 HG01496.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2943+372_2943+374d others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | |||||
| chr12:51495470
|
CT | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2943+374delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | |||||
| chr12:51495542
|
C | G | 59 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0072others(56): Show | 63 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2943+424C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495542 | ||||||
| chr12:51495629
|
C | G | 70 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2943+511C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495629 | ||||||
| chr12:51495773
|
C | T | 4 | a0001c0001t0001g0247a0001c0001t0001g0290a0001c0001t0020g0331others(1): Show | 4 | HG01346.hp1 HG02257.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2943+655C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495773 | ||||||
| chr12:51495827
|
C | T | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2943+709C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495827 | ||||||
| chr12:51495856
|
C | T | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2943+738C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495856 | ||||||
| chr12:51496172
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2944-815G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496172 | ||||||
| chr12:51496349
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2944-638T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496349 | ||||||
| chr12:51496423
|
G | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG01346.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2944-564G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496423 | ||||||
| chr12:51496470
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2944-517G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496470 | ||||||
| chr12:51496505
|
C | G | 2 | a0001c0001t0003g0111a0001c0001t0003g0123 | 2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2944-482C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496505 | ||||||
| chr12:51496810
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2944-177A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496810 | ||||||
| chr12:51496861
|
T | C | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2944-126T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496861 | ||||||
| chr12:51496937
|
G | A | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2944-50G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496937 | ||||||
| chr12:51496973
|
T | A | 7 | a0001c0001t0002g0125a0001c0001t0009g0071a0001c0001t0009g0081others(4): Show | 7 | HG01516.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2944-14T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496973 | ||||||
| chr12:51497483
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0222 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3081+359T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51497483 | ||||||
| chr12:51497568
|
C | T | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3081+444C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51497568 | ||||||
| chr12:51497801
|
G | C | 3 | a0001c0001t0021g0155a0001c0001t0022g0153a0001c0001t0022g0154 | 3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3081+677G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51497801 | ||||||
| chr12:51497864
|
C | CAAAAAAA | 159 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(156): Show | 164 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.3081+745_3081+751d others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51497864 | |||||
| chr12:51497864
|
C | CAAAAAAA others(1): Show |
11 | a0001c0001t0002g0113a0001c0001t0004g0029a0001c0001t0004g0044others(8): Show | 11 | HG01074.hp1 HG02027.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3081+744_3081+751d others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51497864 | |||||
| chr12:51497886
|
G | GA | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3081+770dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51497886 | |||||
| chr12:51498039
|
T | C | 46 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.3081+915T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498039 | ||||||
| chr12:51498060
|
A | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0258others(1): Show | 4 | HG02109.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3081+936A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498060 | ||||||
| chr12:51498138
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3081+1014T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498138 | ||||||
| chr12:51498246
|
A | G | 3 | a0001c0001t0003g0009a0001c0001t0003g0300a0001c0001t0003g0304 | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3081+1122A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498246 | ||||||
| chr12:51498258
|
A | G | 175 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(172): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.3081+1134A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498258 | ||||||
| chr12:51498467
|
A | G | 3 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151 | 3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3081+1343A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498467 | ||||||
| chr12:51498509
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3081+1385C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498509 | ||||||
| chr12:51498606
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3081+1482C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498606 | ||||||
| chr12:51498709
|
C | T | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3081+1585C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498709 | ||||||
| chr12:51498755
|
C | A | 1 | a0001c0001t0029g0278 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3081+1631C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498755 | ||||||
| chr12:51498773
|
C | CGGAGGCT others(707): Show |
1 | a0001c0011t0047g0167 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(718): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(707): Show |
2 | a0001c0001t0004g0029a0001c0001t0004g0056 | 2 | HG04184.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(718): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(707): Show |
3 | a0001c0001t0002g0093a0001c0001t0023g0070a0001c0001t0053g0084 | 3 | HG02056.hp1 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(718): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
2 | a0001c0002t0010g0150a0001c0002t0010g0151 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
1 | a0001c0002t0005g0170 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
29 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(26): Show | 30 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
3 | a0001c0001t0016g0034a0001c0001t0016g0343a0001c0001t0016g0344 | 3 | NA18943.hp2 NA18963.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
41 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
89 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(86): Show | 93 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
42 | a0001c0001t0001g0280a0001c0001t0003g0002a0001c0001t0003g0009others(39): Show | 45 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
1 | a0001c0001t0009g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(706): Show |
1 | a0001c0001t0021g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(705): Show |
1 | a0001c0002t0005g0169 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(705): Show |
1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(705): Show |
124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(121): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(705): Show |
1 | a0001c0001t0040g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(705): Show |
4 | a0001c0001t0021g0156a0001c0001t0022g0153a0001c0001t0022g0154others(1): Show | 4 | HG01884.hp1 HG02809.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498773
|
C | CGGAGGCT others(704): Show |
1 | a0001c0001t0001g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(715): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | |||||
| chr12:51498812
|
G | A | 2 | a0001c0001t0019g0216a0001c0001t0019g0217 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.3081+1688G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498812 | ||||||
| chr12:51498850
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3081+1726A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498850 | ||||||
| chr12:51498879
|
C | CA | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(122): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.3081+1775dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | |||||
| chr12:51498879
|
C | CAA | 46 | a0001c0001t0001g0017a0001c0001t0001g0219a0001c0001t0001g0242others(43): Show | 49 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.3081+1774_3081+177 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | |||||
| chr12:51498879
|
C | CAAA | 149 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(146): Show | 153 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.3081+1773_3081+177 others(7): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | |||||
| chr12:51498879
|
C | CAAAA | 24 | a0001c0001t0002g0074a0001c0001t0002g0076a0001c0001t0002g0080others(21): Show | 25 | HG01981.hp2 HG02056.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.3081+1772_3081+177 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | |||||
| chr12:51499168
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3081+2044A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499168 | ||||||
| chr12:51499318
|
T | C | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3081+2194T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499318 | ||||||
| chr12:51499540
|
A | G | 26 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0111others(23): Show | 28 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3081+2416A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499540 | ||||||
| chr12:51499624
|
T | TAC | 25 | a0001c0001t0002g0004a0001c0001t0002g0089a0001c0001t0002g0090others(22): Show | 26 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081+2533_3081+253 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
T | TACAC | 27 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0260others(24): Show | 27 | HG00558.hp2 HG01074.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.3081+2531_3081+253 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
T | TACACAC | 22 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0200others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.3081+2529_3081+253 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
T | TACACACA others(1): Show |
35 | a0001c0001t0001g0069a0001c0001t0001g0184a0001c0001t0001g0204others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.3081+2527_3081+253 others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
T | TACACACA others(3): Show |
27 | a0001c0001t0001g0190a0001c0001t0001g0202a0001c0001t0001g0206others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3081+2525_3081+253 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
T | TACACACA others(5): Show |
28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0185others(25): Show | 30 | HG00140.hp2 HG00597.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.3081+2523_3081+253 others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
T | TACACACA others(7): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0195others(4): Show | 7 | HG00642.hp1 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.3081+2521_3081+253 others(18): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
TAC | T | 42 | a0001c0001t0002g0072a0001c0001t0002g0076a0001c0001t0002g0086others(39): Show | 43 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.3081+2533_3081+253 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
TACAC | T | 8 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3081+2531_3081+253 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499624
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0002g0112 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3081+2523_3081+253 others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | |||||
| chr12:51499657
|
ACG | A | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0025g0026 | 3 | HG01891.hp2 HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3081+2534_3081+253 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499657 | ||||||
| chr12:51499757
|
G | C | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3081+2633G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499757 | ||||||
| chr12:51499776
|
G | A | 1 | a0001c0001t0003g0321 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3081+2652G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499776 | ||||||
| chr12:51500039
|
G | A | 3 | a0001c0002t0005g0171a0001c0002t0005g0173a0001c0002t0045g0172 | 3 | NA18955.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3081+2915G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500039 | ||||||
| chr12:51500263
|
A | G | 5 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3081+3139A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500263 | ||||||
| chr12:51500276
|
C | T | 1 | a0001c0001t0003g0302 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3081+3152C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500276 | ||||||
| chr12:51500413
|
CTA | C | 3 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0030g0189 | 3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3081+3291_3081+329 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500413 | |||||
| chr12:51500695
|
C | CT | 48 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(45): Show | 48 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.3082-3325dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500695 | |||||
| chr12:51500811
|
C | A | 2 | a0001c0002t0005g0174a0001c0002t0005g0175 | 2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3082-3218C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500811 | ||||||
| chr12:51500838
|
C | A | 2 | a0001c0001t0020g0331a0001c0001t0020g0332 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3082-3191C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500838 | ||||||
| chr12:51500850
|
C | CT | 134 | a0001c0001t0001g0280a0001c0001t0002g0001a0001c0001t0002g0004others(131): Show | 138 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.3082-3166dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500850 | |||||
| chr12:51500850
|
C | CTT | 8 | a0001c0001t0002g0125a0001c0001t0009g0071a0001c0001t0009g0081others(5): Show | 8 | HG01261.hp2 HG01516.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3082-3167_3082-316 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500850 | |||||
| chr12:51500860
|
T | C | 1 | a0001c0002t0010g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3082-3169T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500860 | ||||||
| chr12:51501071
|
C | T | 21 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(18): Show | 21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.3082-2958C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501071 | ||||||
| chr12:51501072
|
G | A | 1 | a0001c0001t0025g0023 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3082-2957G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501072 | ||||||
| chr12:51501129
|
A | G | 175 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(172): Show | 180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.3082-2900A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501129 | ||||||
| chr12:51501315
|
C | T | 1 | a0001c0001t0050g0040 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3082-2714C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501315 | ||||||
| chr12:51501348
|
A | G | 3 | a0001c0001t0021g0155a0001c0001t0022g0153a0001c0001t0022g0154 | 3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3082-2681A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501348 | ||||||
| chr12:51501505
|
C | T | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3082-2524C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501505 | ||||||
| chr12:51501506
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3082-2523G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501506 | ||||||
| chr12:51501517
|
T | G | 4 | a0001c0001t0002g0094a0001c0001t0002g0097a0001c0001t0002g0335others(1): Show | 4 | HG00423.hp2 HG00621.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-2512T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501517 | ||||||
| chr12:51501544
|
T | C | 2 | a0001c0001t0020g0331a0001c0001t0020g0332 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3082-2485T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501544 | ||||||
| chr12:51501846
|
G | A | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3082-2183G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501846 | ||||||
| chr12:51502048
|
A | G | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3082-1981A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502048 | ||||||
| chr12:51502078
|
G | A | 1 | a0001c0001t0004g0345 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3082-1951G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502078 | ||||||
| chr12:51502098
|
C | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(81): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.3082-1931C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502098 | ||||||
| chr12:51502164
|
A | T | 30 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(27): Show | 31 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.3082-1865A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502164 | ||||||
| chr12:51502187
|
A | T | 6 | a0001c0003t0005g0006a0001c0003t0005g0178a0001c0003t0005g0179others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3082-1842A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502187 | ||||||
| chr12:51502233
|
T | TTTTG | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1780_3082-177 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502233 | |||||
| chr12:51502334
|
C | T | 2 | a0001c0001t0042g0148a0001c0001t0043g0149 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-1695C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502334 | ||||||
| chr12:51502354
|
G | T | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1675G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502354 | ||||||
| chr12:51502364
|
T | C | 1 | a0001c0001t0030g0189 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3082-1665T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502364 | ||||||
| chr12:51502485
|
C | T | 7 | a0001c0001t0006g0003a0001c0001t0006g0011a0001c0001t0006g0012others(4): Show | 8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.3082-1544C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502485 | ||||||
| chr12:51502537
|
C | CT | 174 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(171): Show | 179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.3082-1481dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502537 | |||||
| chr12:51502569
|
C | T | 1 | a0001c0001t0048g0022 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3082-1460C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502569 | ||||||
| chr12:51502584
|
G | C | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1445G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502584 | ||||||
| chr12:51502636
|
G | T | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3082-1393G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502636 | ||||||
| chr12:51502773
|
C | T | 2 | a0001c0001t0035g0218a0001c0010t0001g0220 | 2 | HG01192.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3082-1256C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502773 | ||||||
| chr12:51502837
|
A | AT | 13 | a0001c0001t0001g0230a0001c0001t0003g0312a0001c0001t0003g0313others(10): Show | 13 | HG00735.hp1 HG01261.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.3082-1173dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502837 | |||||
| chr12:51502837
|
AT | A | 92 | a0001c0001t0001g0183a0001c0001t0001g0195a0001c0001t0001g0226others(89): Show | 92 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.3082-1173delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502837 | |||||
| chr12:51502864
|
AGTCTCGC others(6): Show |
A | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1161_3082-114 others(17): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502864 | |||||
| chr12:51502881
|
A | G | 308 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3082-1148A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502881 | ||||||
| chr12:51502890
|
G | C | 1 | a0001c0002t0005g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3082-1139G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502890 | ||||||
| chr12:51502903
|
G | A | 1 | a0001c0001t0042g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3082-1126G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502903 | ||||||
| chr12:51502904
|
C | T | 1 | a0001c0001t0042g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3082-1125C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502904 | ||||||
| chr12:51502905
|
C | G | 1 | a0001c0001t0042g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3082-1124C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502905 | ||||||
| chr12:51503040
|
C | T | 46 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0024others(43): Show | 46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.3082-989C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503040 | ||||||
| chr12:51503077
|
C | T | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3082-952C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503077 | ||||||
| chr12:51503149
|
C | T | 1 | a0001c0001t0003g0322 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3082-880C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503149 | ||||||
| chr12:51503229
|
T | A | 83 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(80): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3082-800T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503229 | ||||||
| chr12:51503232
|
A | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(81): Show | 88 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.3082-797A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503232 | ||||||
| chr12:51503234
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3082-795T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503234 | ||||||
| chr12:51503247
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3082-782C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503247 | ||||||
| chr12:51503342
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0012g0212a0001c0001t0012g0270others(1): Show | 4 | NA18747.hp2 NA18978.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-687G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503342 | ||||||
| chr12:51503490
|
C | G | 2 | a0001c0001t0042g0148a0001c0001t0043g0149 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-539C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503490 | ||||||
| chr12:51503561
|
ATTG | A | 3 | a0001c0001t0021g0155a0001c0001t0022g0153a0001c0001t0022g0154 | 3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3082-465_3082-463d others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51503561 | |||||
| chr12:51503588
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3082-441A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503588 | ||||||
| chr12:51503738
|
G | A | 2 | a0001c0001t0014g0015a0001c0001t0014g0016 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3082-291G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503738 | ||||||
| chr12:51503852
|
T | C | 4 | a0001c0002t0010g0019a0001c0002t0010g0150a0001c0002t0010g0151others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-177T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503852 | ||||||
| chr12:51503936
|
A | G | 1 | a0001c0001t0006g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3082-93A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503936 | ||||||
| chr12:51503991
|
C | G | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3082-38C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503991 | ||||||
| chr12:51504230
|
A | G | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3173+110A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504230 | ||||||
| chr12:51504281
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3173+161T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504281 | ||||||
| chr12:51504324
|
G | A | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(138): Show | 145 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3173+204G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504324 | ||||||
| chr12:51504495
|
T | A | 2 | a0001c0001t0002g0063a0001c0001t0002g0067 | 2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3173+375T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504495 | ||||||
| chr12:51504728
|
T | G | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.3173+608T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504728 | ||||||
| chr12:51504922
|
A | G | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3173+802A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504922 | ||||||
| chr12:51504930
|
C | G | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3173+810C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504930 | ||||||
| chr12:51505420
|
A | C | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3174-415A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51505420 | ||||||
| chr12:51505984
|
C | T | 30 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(27): Show | 31 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.3269+54C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51505984 | ||||||
| chr12:51506248
|
A | G | 1 | a0001c0001t0007g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3269+318A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506248 | ||||||
| chr12:51506321
|
C | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3269+391C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506321 | ||||||
| chr12:51506358
|
C | T | 1 | a0001c0001t0015g0136 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3269+428C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506358 | ||||||
| chr12:51506400
|
G | GT | 10 | a0001c0001t0001g0223a0001c0001t0003g0301a0001c0001t0009g0071others(7): Show | 10 | HG00741.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3269+480dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr12 | 51506400 | |||||
| chr12:51506411
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3269+481C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506411 | ||||||
| chr12:51506704
|
G | A | 5 | a0001c0001t0021g0155a0001c0001t0021g0156a0001c0001t0022g0153others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3270-722G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506704 | ||||||
| chr12:51506734
|
G | A | 34 | a0001c0002t0005g0157a0001c0002t0005g0158a0001c0002t0005g0159others(31): Show | 35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.3270-692G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506734 | ||||||
| chr12:51506962
|
T | A | 1 | a0001c0001t0003g0314 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3270-464T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506962 | ||||||
| chr12:51507272
|
G | A | 7 | a0001c0001t0006g0003a0001c0001t0006g0011a0001c0001t0006g0012others(4): Show | 8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.3270-154G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51507272 |