Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 115111 |
| ensemblid | ENSG00000147606.9 |
| hgncid | 14467 |
| symbol | SLC26A7 |
| name | solute carrier family 26 member 7 |
| refseq_nuc | NM_052832.4 |
| refseq_prot | NP_439897.1 |
| ensembl_nuc | ENST00000276609.8 |
| ensembl_prot | ENSP00000276609.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 91249319 |
| end | 91398155 |
| strand | + |
| ver | v1.2 |
| region | chr8:91249319-91398155 |
| region5000 | chr8:91244319-91403155 |
| regionname0 | SLC26A7_chr8_91249319_91398155 |
| regionname5000 | SLC26A7_chr8_91244319_91403155 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 656 | 199 | 72 | 55 | 44 | 6 | 21 | 28 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | MTGAK others(651): Show |
chr8 | 91244319 | 91403155 |
| a0002 | 0/1 | 656 | 7 | 3 | 1 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | MTGAK others(651): Show |
chr8 | 91244319 | 91403155 |
| a0003 | 0/0 | 656 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | MTGAK others(651): Show |
chr8 | 91244319 | 91403155 |
| a0004 | 0/0 | 656 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | MTGAK others(651): Show |
chr8 | 91244319 | 91403155 |
| a0005 | 0/0 | 656 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | MTGAK others(651): Show |
chr8 | 91244319 | 91403155 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1968 | 148 | 46 | 40 | 41 | 5 | 15 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0001c0002 | 0/0 | 1968 | 44 | 23 | 15 | 1 | 1 | 4 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0001c0004 | 0/0 | 1968 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0001c0005 | 0/0 | 1968 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0001c0007 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0001c0008 | 0/0 | 1968 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0001c0012 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0002c0003 | 0/1 | 1968 | 7 | 3 | 1 | 0 | 2 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0003c0006 | 0/0 | 1968 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0003c0009 | 0/0 | 1968 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0004c0011 | 0/0 | 1968 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 | ||
| a0005c0010 | 0/0 | 1968 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | ATGAC others(1963): Show |
chr8 | 91244319 | 91403155 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5237 | 118 | 27 | 35 | 36 | 5 | 14 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0002 | 0/0 | 5237 | 7 | 4 | 2 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0003 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0004 | 0/0 | 5237 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0005 | 0/0 | 5237 | 4 | 3 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0007 | 0/0 | 5237 | 3 | 0 | 0 | 3 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0009 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0010 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0012 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0013 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0017 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0018 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0020 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0021 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0001t0023 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0001 | 0/0 | 5237 | 19 | 9 | 8 | 0 | 0 | 2 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0002 | 0/0 | 5237 | 9 | 2 | 4 | 1 | 1 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0003 | 0/0 | 5237 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0004 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0005 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0006 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0008 | 0/0 | 5237 | 3 | 0 | 2 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0009 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0012 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0015 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0002t0022 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0004t0002 | 0/0 | 5237 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0005t0006 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0007t0002 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0008t0001 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0001c0012t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0002c0003t0001 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0002c0003t0004 | 0/0 | 5237 | 3 | 0 | 1 | 0 | 2 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0002c0003t0016 | 0/1 | 5237 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0002c0003t0019 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0003c0006t0011 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5231): Show |
chr8 | 91244319 | 91403155 |
| a0003c0009t0011 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5231): Show |
chr8 | 91244319 | 91403155 |
| a0004c0011t0014 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| a0005c0010t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | GTAGA others(5232): Show |
chr8 | 91244319 | 91403155 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0017g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0018g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0001t0023g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0008g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0012g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0002t0022g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0004t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0005t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0005t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0007t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0008t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0016g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0002c0003t0019g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0003c0006t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0003c0009t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0004c0011t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| a0005c0010t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0120 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0095 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00733 | hp2 | a0001 | c0002 | t0008 | g0190 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00735 | hp1 | a0001 | c0002 | t0012 | g0100 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0146 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0051 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01891 | hp1 | a0004 | c0011 | t0014 | g0022 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01934 | hp1 | a0001 | c0002 | t0008 | g0189 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01993 | hp1 | a0001 | c0001 | t0017 | g0192 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02055 | hp1 | a0003 | c0006 | t0011 | g0069 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0088 | EAS | CDX | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02257 | hp1 | a0001 | c0002 | t0006 | g0019 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0117 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0031 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0094 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0203 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0124 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02886 | hp2 | a0001 | c0001 | t0023 | g0104 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0092 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0093 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02970 | hp1 | a0001 | c0002 | t0009 | g0102 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02970 | hp2 | a0001 | c0005 | t0006 | g0109 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0136 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03130 | hp1 | a0001 | c0002 | t0022 | g0023 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0135 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0201 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03516 | hp1 | a0001 | c0002 | t0015 | g0024 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03927 | hp2 | a0001 | c0002 | t0008 | g0158 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03942 | hp2 | a0005 | c0010 | t0001 | g0074 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04184 | hp1 | a0001 | c0012 | t0001 | g0075 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04184 | hp2 | a0001 | c0007 | t0002 | g0195 | SAS | BEB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0206 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18947 | hp2 | a0001 | c0004 | t0002 | g0159 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18963 | hp1 | a0001 | c0004 | t0002 | g0144 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18966 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19006 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0204 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20752 | hp1 | a0002 | c0003 | t0004 | g0156 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0148 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20805 | hp1 | a0002 | c0003 | t0004 | g0157 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG02486 | hp2 | a0002 | c0003 | t0019 | g0009 | AFR | ACB | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | MSL | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| HG06807 | hp2 | a0001 | c0005 | t0006 | g0106 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA20300 | hp2 | a0003 | c0009 | t0011 | g0138 | AFR | USA | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0016 | g0155 | REF | REF | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0175 | REF | REF | SLC26A7_chr8_91244319_91403155 | SLC26A7 | chr8 | 91244319 | 91403155 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91318250 | C | T | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.512C>T | p.Thr171Ile | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/19 | 720/5237 | 512/1971 | 171/656 | chr8 | 91318250 | |||
| chr8:91334295 | A | G | 1 | a0002 | 6 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.643A>G | p.Ile215Val | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/19 | 851/5237 | 643/1971 | 215/656 | chr8 | 91334295 | |||
| chr8:91363504 | A | T | 1 | a0005 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1454A>T | p.Glu485Val | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/19 | 1662/5237 | 1454/1971 | 485/656 | chr8 | 91363504 | |||
| chr8:91389374 | A | C | 1 | a0003 | 2 | HG02055.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1712A>C | p.Tyr571Ser | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/19 | 1920/5237 | 1712/1971 | 571/656 | chr8 | 91389374 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91295565 | C | T | 1 | a0001c0012 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.339C>T | p.Asn113Asn | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/19 | 547/5237 | 339/1971 | 113/656 | chr8 | 91295565 | |||
| chr8:91351872 | T | C | 3 | a0001c0002 a0001c0004 a0003c0006 |
47 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(44): Show |
synonymous_variant | LOW | c.1203T>C | p.Leu401Leu | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/19 | 1411/5237 | 1203/1971 | 401/656 | chr8 | 91351872 | |||
| chr8:91362412 | G | A | 1 | a0001c0007 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1374G>A | p.Leu458Leu | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/19 | 1582/5237 | 1374/1971 | 458/656 | chr8 | 91362412 | |||
| chr8:91393841 | C | T | 1 | a0001c0004 | 2 | NA18947.hp2 NA18963.hp1 |
synonymous_variant | LOW | c.1821C>T | p.Ala607Ala | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 17/19 | 2029/5237 | 1821/1971 | 607/656 | chr8 | 91393841 | |||
| chr8:91394003 | G | A | 1 | a0001c0005 | 2 | HG02970.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.1899G>A | p.Ser633Ser | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/19 | 2107/5237 | 1899/1971 | 633/656 | chr8 | 91394003 | |||
| chr8:91394012 | T | C | 1 | a0001c0008 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1908T>C | p.Ala636Ala | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/19 | 2116/5237 | 1908/1971 | 636/656 | chr8 | 91394012 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91395105 | T | C | 2 | a0003c0006t0011 a0003c0009t0011 |
2 | HG02055.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 8 | chr8 | 91395105 | ||||||
| chr8:91395218 | C | T | 7 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(4): Show |
22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*121C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 121 | chr8 | 91395218 | ||||||
| chr8:91395247 | G | A | 1 | a0001c0001t0013 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 150 | chr8 | 91395247 | ||||||
| chr8:91395296 | G | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
37 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*199G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 199 | chr8 | 91395296 | ||||||
| chr8:91395471 | G | T | 7 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(4): Show |
22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*374G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 374 | chr8 | 91395471 | ||||||
| chr8:91395562 | C | T | 3 | a0001c0001t0012 a0001c0002t0012 a0001c0002t0022 |
3 | HG00735.hp1 HG02572.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*465C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 465 | chr8 | 91395562 | ||||||
| chr8:91395677 | C | T | 1 | a0001c0001t0021 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 580 | chr8 | 91395677 | ||||||
| chr8:91395883 | A | G | 1 | a0001c0001t0010 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*786A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 786 | chr8 | 91395883 | ||||||
| chr8:91395936 | A | G | 1 | a0001c0001t0020 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 839 | chr8 | 91395936 | ||||||
| chr8:91396017 | A | G | 2 | a0001c0001t0009 a0001c0002t0009 |
3 | HG02970.hp1 HG03041.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*920A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 920 | chr8 | 91396017 | ||||||
| chr8:91396102 | T | G | 7 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(4): Show |
22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1005T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1005 | chr8 | 91396102 | ||||||
| chr8:91396110 | A | G | 1 | a0001c0002t0015 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1013 | chr8 | 91396110 | ||||||
| chr8:91396226 | T | C | 2 | a0001c0001t0005 a0001c0002t0005 |
5 | HG01109.hp2 HG01884.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1129T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1129 | chr8 | 91396226 | ||||||
| chr8:91396755 | G | C | 1 | a0001c0002t0022 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1658 | chr8 | 91396755 | ||||||
| chr8:91396819 | C | T | 9 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0023 others(6): Show |
24 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1722C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1722 | chr8 | 91396819 | ||||||
| chr8:91396842 | T | C | 7 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(4): Show |
22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1745T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1745 | chr8 | 91396842 | ||||||
| chr8:91396867 | G | A | 3 | a0001c0001t0023 a0003c0006t0011 a0003c0009t0011 |
3 | HG02055.hp1 HG02886.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1770 | chr8 | 91396867 | ||||||
| chr8:91396910 | G | A | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(1): Show |
19 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1813G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1813 | chr8 | 91396910 | ||||||
| chr8:91397053 | G | A | 1 | a0001c0001t0007 | 3 | HG00558.hp2 NA19006.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1956G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 1956 | chr8 | 91397053 | ||||||
| chr8:91397193 | T | C | 1 | a0001c0001t0018 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2096 | chr8 | 91397193 | ||||||
| chr8:91397200 | T | G | 1 | a0001c0002t0008 | 3 | HG00733.hp2 HG01934.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2103T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2103 | chr8 | 91397200 | ||||||
| chr8:91397220 | G | A | 3 | a0001c0001t0003 a0001c0002t0003 a0004c0011t0014 |
8 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2123G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2123 | chr8 | 91397220 | ||||||
| chr8:91397271 | GT | G | 2 | a0003c0006t0011 a0003c0009t0011 |
2 | HG02055.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2175delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2175 | chr8 | 91397271 | ||||||
| chr8:91397311 | G | A | 3 | a0001c0001t0003 a0001c0002t0003 a0004c0011t0014 |
8 | HG01891.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2214G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2214 | chr8 | 91397311 | ||||||
| chr8:91397313 | C | T | 1 | a0004c0011t0014 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2216 | chr8 | 91397313 | ||||||
| chr8:91397469 | G | A | 7 | a0001c0001t0002 a0001c0001t0023 a0001c0002t0002 others(4): Show |
22 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2372G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2372 | chr8 | 91397469 | ||||||
| chr8:91397527 | G | T | 1 | a0001c0001t0017 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2430 | chr8 | 91397527 | ||||||
| chr8:91397841 | A | G | 2 | a0001c0001t0003 a0001c0002t0003 |
7 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2744A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2744 | chr8 | 91397841 | ||||||
| chr8:91397861 | A | G | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0003 others(3): Show |
14 | HG00642.hp1 HG00738.hp1 HG01891.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2764A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2764 | chr8 | 91397861 | ||||||
| chr8:91397962 | A | C | 2 | a0001c0002t0006 a0001c0005t0006 |
4 | HG02257.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2865A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 19/19 | 2865 | chr8 | 91397962 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91249477 | A | G | 9 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(6): Show |
9 | HG02257.hp2 HG02809.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-113-62A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 1/18 | chr8 | 91249477 | |||||||
| chr8:91249495 | A | ATC | 3 | a0001c0001t0005g0004 a0001c0001t0007g0005 a0001c0001t0007g0006 |
3 | HG01109.hp2 NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-113-26_-113-25dup others(2): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 91249495 | ||||||
| chr8:91250057 | T | G | 2 | a0001c0001t0001g0008 a0001c0001t0002g0007 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.193+213T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91250057 | |||||||
| chr8:91250656 | T | G | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.193+812T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91250656 | |||||||
| chr8:91250933 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0002t0001g0197 others(1): Show |
5 | HG00735.hp2 HG00738.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+1089C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91250933 | |||||||
| chr8:91251047 | AT | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(131): Show |
136 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.193+1213delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91251047 | ||||||
| chr8:91251253 | A | G | 16 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0115 others(13): Show |
16 | HG00558.hp2 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+1409A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251253 | |||||||
| chr8:91251455 | A | T | 1 | a0001c0001t0009g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193+1611A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251455 | |||||||
| chr8:91251672 | C | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+1828C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251672 | |||||||
| chr8:91251804 | C | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0030 others(87): Show |
92 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.193+1960C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91251804 | |||||||
| chr8:91252102 | T | C | 1 | a0001c0002t0002g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193+2258T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252102 | |||||||
| chr8:91252155 | T | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(152): Show |
158 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.193+2311T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252155 | |||||||
| chr8:91252378 | C | A | 2 | a0001c0001t0018g0124 a0001c0002t0003g0125 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.193+2534C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252378 | |||||||
| chr8:91252552 | G | T | 9 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0194 others(6): Show |
9 | HG00558.hp2 HG01123.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+2708G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252552 | |||||||
| chr8:91252735 | A | T | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+2891A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252735 | |||||||
| chr8:91252940 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.193+3096A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91252940 | |||||||
| chr8:91253295 | C | T | 52 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(49): Show |
52 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.193+3451C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253295 | |||||||
| chr8:91253400 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.193+3556T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253400 | |||||||
| chr8:91253405 | C | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3561C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253405 | |||||||
| chr8:91253410 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.193+3566A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253410 | |||||||
| chr8:91253464 | C | T | 4 | a0001c0001t0001g0018 a0001c0002t0015g0024 a0001c0002t0022g0023 others(1): Show |
4 | HG01261.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+3620C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253464 | |||||||
| chr8:91253504 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+3660A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253504 | |||||||
| chr8:91253755 | C | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(8): Show |
11 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+3911C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91253755 | |||||||
| chr8:91254079 | T | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0005g0004 others(6): Show |
9 | HG01070.hp2 HG01109.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+4235T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254079 | |||||||
| chr8:91254250 | G | A | 2 | a0001c0001t0001g0145 a0001c0004t0002g0144 |
2 | NA18963.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.193+4406G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254250 | |||||||
| chr8:91254576 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+4732T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254576 | |||||||
| chr8:91254683 | G | A | 2 | a0001c0001t0001g0119 a0001c0002t0002g0121 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.193+4839G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254683 | |||||||
| chr8:91254735 | T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+4891T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91254735 | |||||||
| chr8:91255055 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.193+5211A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255055 | |||||||
| chr8:91255190 | T | C | 16 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+5346T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255190 | |||||||
| chr8:91255263 | A | G | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+5419A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255263 | |||||||
| chr8:91255329 | A | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+5485A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255329 | |||||||
| chr8:91255529 | C | G | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+5685C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255529 | |||||||
| chr8:91255581 | A | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+5737A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255581 | |||||||
| chr8:91255803 | A | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+5959A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255803 | |||||||
| chr8:91255982 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193+6138T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91255982 | |||||||
| chr8:91256150 | C | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0072 |
3 | HG03195.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.193+6306C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256150 | |||||||
| chr8:91256304 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+6460C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256304 | |||||||
| chr8:91256397 | A | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+6553A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256397 | |||||||
| chr8:91256676 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.193+6832G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91256676 | |||||||
| chr8:91257167 | A | G | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+7323A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257167 | |||||||
| chr8:91257595 | C | A | 3 | a0001c0001t0001g0111 a0001c0002t0001g0110 a0001c0002t0001g0112 |
3 | HG01081.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.193+7751C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257595 | |||||||
| chr8:91257626 | A | T | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193+7782A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257626 | |||||||
| chr8:91257635 | A | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0114 a0001c0001t0001g0115 others(9): Show |
13 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.193+7791A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257635 | |||||||
| chr8:91257729 | G | C | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193+7885G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257729 | |||||||
| chr8:91257928 | A | G | 2 | a0001c0001t0001g0071 a0001c0002t0002g0070 |
2 | NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.193+8084A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257928 | |||||||
| chr8:91257935 | C | T | 2 | a0001c0001t0001g0137 a0003c0006t0011g0069 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.193+8091C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91257935 | |||||||
| chr8:91258007 | A | G | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+8163A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258007 | |||||||
| chr8:91258428 | G | C | 2 | a0001c0001t0001g0191 a0001c0001t0017g0192 |
2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.193+8584G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258428 | |||||||
| chr8:91258637 | T | C | 2 | a0001c0001t0001g0119 a0001c0002t0002g0121 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.193+8793T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258637 | |||||||
| chr8:91258662 | TAA | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+8819_193+8820d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258662 | |||||||
| chr8:91258682 | C | G | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+8838C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258682 | |||||||
| chr8:91258963 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.193+9119C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258963 | |||||||
| chr8:91258964 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+9120G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91258964 | |||||||
| chr8:91259281 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.193+9437C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259281 | |||||||
| chr8:91259354 | G | A | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+9510G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259354 | |||||||
| chr8:91259364 | G | T | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+9520G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259364 | |||||||
| chr8:91259481 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+9637G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259481 | |||||||
| chr8:91259635 | C | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.193+9791C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259635 | |||||||
| chr8:91259739 | A | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+9895A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259739 | |||||||
| chr8:91259739 | A | T | 22 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(19): Show |
22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.193+9895A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259739 | |||||||
| chr8:91259749 | A | G | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+9905A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259749 | |||||||
| chr8:91259767 | G | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193+9923G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259767 | |||||||
| chr8:91259895 | T | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.193+10051T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259895 | |||||||
| chr8:91259909 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.193+10065T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91259909 | |||||||
| chr8:91260046 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193+10202T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260046 | |||||||
| chr8:91260156 | A | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0002t0002g0070 |
3 | HG02523.hp2 NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.193+10312A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260156 | |||||||
| chr8:91260318 | G | A | 60 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(57): Show |
60 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.193+10474G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260318 | |||||||
| chr8:91260437 | C | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+10593C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260437 | |||||||
| chr8:91260973 | C | T | 3 | a0001c0001t0010g0092 a0001c0001t0010g0093 a0001c0001t0010g0094 |
3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.193+11129C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91260973 | |||||||
| chr8:91261088 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0009g0201 |
3 | HG02896.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.193+11244G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261088 | |||||||
| chr8:91261108 | T | G | 1 | a0005c0010t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.193+11264T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261108 | |||||||
| chr8:91261432 | G | C | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+11588G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261432 | |||||||
| chr8:91261485 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.193+11641G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261485 | |||||||
| chr8:91261568 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.193+11724G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261568 | |||||||
| chr8:91261734 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.193+11890G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91261734 | |||||||
| chr8:91262002 | C | T | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+12158C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262002 | |||||||
| chr8:91262138 | C | T | 2 | a0001c0001t0001g0071 a0001c0002t0002g0070 |
2 | NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.193+12294C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262138 | |||||||
| chr8:91262451 | A | G | 16 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+12607A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262451 | |||||||
| chr8:91262554 | C | G | 8 | a0001c0001t0001g0010 a0001c0001t0005g0108 a0001c0001t0018g0124 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+12710C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262554 | |||||||
| chr8:91262892 | T | A | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+13048T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262892 | |||||||
| chr8:91262919 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+13075C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91262919 | |||||||
| chr8:91263041 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193+13197C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263041 | |||||||
| chr8:91263068 | C | T | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.193+13224C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263068 | |||||||
| chr8:91263234 | A | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG00558.hp1 NA18960.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+13390A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263234 | |||||||
| chr8:91263540 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+13696C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263540 | |||||||
| chr8:91263576 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.193+13732G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263576 | |||||||
| chr8:91263644 | C | T | 22 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(19): Show |
22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.193+13800C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263644 | |||||||
| chr8:91263680 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.193+13836G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91263680 | |||||||
| chr8:91263966 | AT | A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(19): Show |
22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.193+14131delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91263966 | ||||||
| chr8:91264606 | C | T | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193+14762C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264606 | |||||||
| chr8:91264657 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.193+14813G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264657 | |||||||
| chr8:91264722 | G | A | 3 | a0001c0001t0004g0202 a0001c0001t0012g0117 a0001c0002t0004g0203 |
3 | HG02257.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.193+14878G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264722 | |||||||
| chr8:91264748 | A | T | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+14904A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264748 | |||||||
| chr8:91264995 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.193+15151C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91264995 | |||||||
| chr8:91265154 | G | T | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+15310G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265154 | |||||||
| chr8:91265377 | C | T | 4 | a0001c0001t0001g0030 a0001c0002t0015g0024 a0001c0002t0022g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+15533C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265377 | |||||||
| chr8:91265537 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(59): Show |
63 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.193+15693T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265537 | |||||||
| chr8:91265724 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193+15880T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265724 | |||||||
| chr8:91265740 | T | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+15896T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265740 | |||||||
| chr8:91265761 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.193+15917G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265761 | |||||||
| chr8:91265893 | T | G | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193+16049T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91265893 | |||||||
| chr8:91266161 | A | T | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193+16317A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266161 | |||||||
| chr8:91266178 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193+16334C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266178 | |||||||
| chr8:91266219 | G | A | 3 | a0001c0001t0005g0004 a0001c0002t0002g0046 a0001c0002t0002g0047 |
3 | HG01070.hp2 HG01109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.193+16375G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266219 | |||||||
| chr8:91266327 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+16483G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266327 | |||||||
| chr8:91266446 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.193+16602A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91266446 | |||||||
| chr8:91267055 | T | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+17211T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267055 | |||||||
| chr8:91267060 | A | G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+17216A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267060 | |||||||
| chr8:91267070 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(157): Show |
163 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.193+17226T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267070 | |||||||
| chr8:91267105 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+17261T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267105 | |||||||
| chr8:91267207 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.193+17363T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267207 | |||||||
| chr8:91267271 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.193+17427T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267271 | |||||||
| chr8:91267283 | G | A | 1 | a0001c0012t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193+17439G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267283 | |||||||
| chr8:91267360 | A | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+17516A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267360 | |||||||
| chr8:91267509 | T | C | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+17665T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267509 | |||||||
| chr8:91267660 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(147): Show |
153 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.193+17816A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267660 | |||||||
| chr8:91267681 | T | C | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.193+17837T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267681 | |||||||
| chr8:91267910 | C | T | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.193+18066C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91267910 | |||||||
| chr8:91268335 | T | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.193+18491T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268335 | |||||||
| chr8:91268434 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.193+18590T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268434 | |||||||
| chr8:91268560 | A | T | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.193+18716A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268560 | |||||||
| chr8:91268678 | T | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+18834T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268678 | |||||||
| chr8:91268684 | G | C | 1 | a0001c0001t0012g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.193+18840G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268684 | |||||||
| chr8:91268885 | T | A | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+19041T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91268885 | |||||||
| chr8:91268943 | CA | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(149): Show |
155 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.193+19109delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91268943 | ||||||
| chr8:91269027 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193+19183T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269027 | |||||||
| chr8:91269223 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.193+19379A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269223 | |||||||
| chr8:91269294 | C | CAG | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+19451_193+1945 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91269294 | ||||||
| chr8:91269407 | G | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.193+19563G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269407 | |||||||
| chr8:91269507 | A | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-19629A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269507 | |||||||
| chr8:91269707 | T | A | 5 | a0001c0001t0001g0101 a0001c0001t0005g0099 a0001c0002t0001g0103 others(2): Show |
5 | HG00735.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-19429T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269707 | |||||||
| chr8:91269906 | A | AT | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-19225dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91269906 | ||||||
| chr8:91269937 | A | G | 4 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-19199A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269937 | |||||||
| chr8:91269947 | T | C | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.194-19189T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91269947 | |||||||
| chr8:91270080 | A | G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-19056A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270080 | |||||||
| chr8:91270087 | T | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-19049T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270087 | |||||||
| chr8:91270123 | T | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-19013T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270123 | |||||||
| chr8:91270261 | T | C | 3 | a0001c0002t0015g0024 a0001c0002t0022g0023 a0004c0011t0014g0022 |
3 | HG01891.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194-18875T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270261 | |||||||
| chr8:91270271 | G | A | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-18865G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270271 | |||||||
| chr8:91270372 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.194-18764G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270372 | |||||||
| chr8:91270405 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-18731A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270405 | |||||||
| chr8:91270525 | T | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-18611T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270525 | |||||||
| chr8:91270682 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.194-18454A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270682 | |||||||
| chr8:91270706 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.194-18430T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91270706 | |||||||
| chr8:91271003 | A | G | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-18133A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271003 | |||||||
| chr8:91271103 | G | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-18033G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271103 | |||||||
| chr8:91271167 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.194-17969T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271167 | |||||||
| chr8:91271238 | G | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-17898G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271238 | |||||||
| chr8:91271371 | G | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-17765G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271371 | |||||||
| chr8:91271402 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17734C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271402 | |||||||
| chr8:91271590 | C | CT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0050 others(13): Show |
17 | HG00438.hp1 HG00609.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-17524dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | ||||||
| chr8:91271590 | C | CTT | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0009g0201 others(3): Show |
6 | HG02572.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-17525_194-1752 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | ||||||
| chr8:91271590 | CTTT | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17526_194-1752 others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | ||||||
| chr8:91271590 | CTTTT | C | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-17527_194-1752 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91271590 | ||||||
| chr8:91271626 | G | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17510G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271626 | |||||||
| chr8:91271719 | C | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-17417C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271719 | |||||||
| chr8:91271796 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.194-17340G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271796 | |||||||
| chr8:91271828 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.194-17308T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271828 | |||||||
| chr8:91271978 | G | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17158G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91271978 | |||||||
| chr8:91272011 | A | G | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-17125A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272011 | |||||||
| chr8:91272195 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-16941T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272195 | |||||||
| chr8:91272365 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-16771A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272365 | |||||||
| chr8:91272537 | C | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-16599C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272537 | |||||||
| chr8:91272766 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.194-16370T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272766 | |||||||
| chr8:91272949 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.194-16187T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272949 | |||||||
| chr8:91272981 | C | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-16155C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91272981 | |||||||
| chr8:91273018 | G | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-16118G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273018 | |||||||
| chr8:91273166 | A | T | 6 | a0001c0001t0001g0013 a0001c0002t0003g0011 a0001c0002t0003g0017 others(3): Show |
6 | HG02622.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-15970A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273166 | |||||||
| chr8:91273193 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.194-15943G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273193 | |||||||
| chr8:91273207 | G | A | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-15929G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273207 | |||||||
| chr8:91273494 | A | G | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-15642A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273494 | |||||||
| chr8:91273675 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-15461C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273675 | |||||||
| chr8:91273999 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-15137T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91273999 | |||||||
| chr8:91274003 | G | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-15133G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274003 | |||||||
| chr8:91274017 | G | A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(19): Show |
22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-15119G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274017 | |||||||
| chr8:91274060 | T | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-15076T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274060 | |||||||
| chr8:91274155 | G | A | 1 | a0001c0002t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.194-14981G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274155 | |||||||
| chr8:91274265 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.194-14871G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274265 | |||||||
| chr8:91274354 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0003g0133 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-14782T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274354 | |||||||
| chr8:91274442 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-14694G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274442 | |||||||
| chr8:91274470 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-14666G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274470 | |||||||
| chr8:91274900 | A | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-14236A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91274900 | |||||||
| chr8:91275037 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.194-14099G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275037 | |||||||
| chr8:91275182 | C | T | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.194-13954C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275182 | |||||||
| chr8:91275189 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.194-13947T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275189 | |||||||
| chr8:91275282 | A | G | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194-13854A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275282 | |||||||
| chr8:91275416 | C | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-13720C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275416 | |||||||
| chr8:91275556 | T | A | 1 | a0001c0002t0001g0080 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.194-13580T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275556 | |||||||
| chr8:91275618 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0091 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13518C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275618 | |||||||
| chr8:91275679 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-13457A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275679 | |||||||
| chr8:91275688 | G | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-13448G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275688 | |||||||
| chr8:91275737 | C | T | 4 | a0001c0001t0001g0030 a0001c0002t0015g0024 a0001c0002t0022g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-13399C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275737 | |||||||
| chr8:91275792 | G | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-13344G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275792 | |||||||
| chr8:91275875 | A | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-13261A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275875 | |||||||
| chr8:91275881 | G | A | 5 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0003t0004g0095 others(2): Show |
5 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-13255G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275881 | |||||||
| chr8:91275908 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.194-13228T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275908 | |||||||
| chr8:91275965 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-13171C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91275965 | |||||||
| chr8:91276005 | T | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-13131T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276005 | |||||||
| chr8:91276074 | C | G | 3 | a0001c0001t0001g0111 a0001c0002t0001g0110 a0001c0002t0001g0112 |
3 | HG01081.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194-13062C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276074 | |||||||
| chr8:91276236 | TAAAA | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-12898_194-1289 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91276236 | ||||||
| chr8:91276382 | T | C | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-12754T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276382 | |||||||
| chr8:91276419 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.194-12717T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276419 | |||||||
| chr8:91276452 | C | T | 2 | a0001c0002t0015g0024 a0001c0002t0022g0023 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194-12684C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276452 | |||||||
| chr8:91276505 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-12631G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276505 | |||||||
| chr8:91276516 | C | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-12620C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276516 | |||||||
| chr8:91276650 | T | C | 16 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.194-12486T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276650 | |||||||
| chr8:91276794 | G | C | 61 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(58): Show |
61 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.194-12342G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276794 | |||||||
| chr8:91276975 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.194-12161C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91276975 | |||||||
| chr8:91277078 | A | G | 1 | a0001c0001t0009g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.194-12058A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277078 | |||||||
| chr8:91277104 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02818.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-12032C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277104 | |||||||
| chr8:91277143 | C | A | 6 | a0001c0001t0001g0010 a0001c0001t0005g0108 a0001c0001t0018g0124 others(3): Show |
6 | HG02145.hp1 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-11993C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277143 | |||||||
| chr8:91277289 | A | G | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-11847A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277289 | |||||||
| chr8:91277317 | C | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.194-11819C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277317 | |||||||
| chr8:91277389 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-11747C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277389 | |||||||
| chr8:91277840 | CAA | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-11295_194-1129 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277840 | |||||||
| chr8:91277903 | C | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-11233C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277903 | |||||||
| chr8:91277904 | CAT | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-11227_194-1122 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91277904 | ||||||
| chr8:91277912 | A | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-11224A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91277912 | |||||||
| chr8:91278087 | A | G | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-11049A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278087 | |||||||
| chr8:91278230 | G | GA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-10896dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91278230 | ||||||
| chr8:91278230 | GA | G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-10896delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91278230 | ||||||
| chr8:91278300 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-10836G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278300 | |||||||
| chr8:91278416 | G | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(25): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-10720G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278416 | |||||||
| chr8:91278540 | T | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-10596T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278540 | |||||||
| chr8:91278613 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-10523A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278613 | |||||||
| chr8:91278726 | C | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-10410C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278726 | |||||||
| chr8:91278794 | A | G | 51 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(48): Show |
51 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.194-10342A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278794 | |||||||
| chr8:91278828 | A | G | 61 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(58): Show |
61 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.194-10308A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278828 | |||||||
| chr8:91278837 | G | A | 3 | a0001c0001t0004g0202 a0001c0001t0012g0117 a0001c0002t0004g0203 |
3 | HG02257.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.194-10299G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91278837 | |||||||
| chr8:91279058 | A | G | 1 | a0001c0001t0007g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.194-10078A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279058 | |||||||
| chr8:91279059 | T | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-10077T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279059 | |||||||
| chr8:91279123 | GTGTATAT others(5): Show |
G | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.194-10011_194-1000 others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279123 | ||||||
| chr8:91279125 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0140 others(5): Show |
8 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-10011G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279125 | |||||||
| chr8:91279125 | G | GTA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.194-9971_194-9970d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTATA | 24 | a0001c0001t0001g0043 a0001c0001t0001g0128 a0001c0001t0001g0151 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.194-9973_194-9970d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTATATA | 5 | a0001c0001t0001g0154 a0001c0001t0001g0181 a0001c0001t0001g0199 others(2): Show |
5 | HG01123.hp1 HG02896.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-9975_194-9970d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0182 |
3 | HG02300.hp2 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.194-9977_194-9970d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTATATAT others(3): Show |
5 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0004g0188 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-9979_194-9970d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTATATAT others(5): Show |
1 | a0001c0001t0009g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.194-9981_194-9970d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTGTATA | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194-10010_194-1000 others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTGTGTAT others(1): Show |
3 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0002t0002g0121 |
3 | HG02895.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTGTGTAT others(3): Show |
3 | a0001c0001t0007g0005 a0001c0001t0007g0006 a0001c0005t0006g0106 |
3 | HG06807.hp2 NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | G | GTGTGTGT others(3): Show |
3 | a0001c0001t0001g0119 a0001c0001t0005g0004 a0001c0002t0002g0047 |
3 | HG01109.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.194-10010_194-1000 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTA | G | 5 | a0001c0001t0001g0010 a0001c0001t0002g0001 a0001c0001t0002g0072 others(2): Show |
6 | HG02004.hp2 HG02145.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-9971_194-9970d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATA | G | 16 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0050 others(13): Show |
16 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-9973_194-9970d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATA | G | 16 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0056 others(13): Show |
16 | HG00280.hp2 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.194-9975_194-9970d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(1): Show |
G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(37): Show |
41 | HG00438.hp2 HG00609.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.194-9977_194-9970d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(3): Show |
G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0089 others(4): Show |
7 | HG01243.hp1 HG01978.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-9979_194-9970d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-9981_194-9970d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(7): Show |
G | 2 | a0001c0001t0002g0176 a0001c0001t0004g0202 |
2 | HG02148.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.194-9983_194-9970d others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(15): Show |
G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.194-9991_194-9970d others(24): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(17): Show |
G | 1 | a0002c0003t0004g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.194-9993_194-9970d others(26): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279125 | GTATATAT others(21): Show |
G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-9997_194-9970d others(30): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279125 | ||||||
| chr8:91279127 | A | G | 4 | a0001c0001t0018g0124 a0001c0002t0001g0186 a0001c0002t0002g0146 others(1): Show |
4 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-10009A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279127 | |||||||
| chr8:91279129 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0018g0124 a0001c0002t0001g0186 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-10007A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279129 | |||||||
| chr8:91279131 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0061 others(6): Show |
9 | HG00741.hp2 HG01081.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-10005A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279131 | |||||||
| chr8:91279133 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.194-9986_194-9985i others(20): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279133 | ||||||
| chr8:91279133 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0002t0001g0110 others(3): Show |
6 | HG01081.hp2 HG01255.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-10003A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279133 | |||||||
| chr8:91279135 | A | G | 2 | a0001c0001t0001g0010 a0001c0008t0001g0031 |
2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.194-10001A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279135 | |||||||
| chr8:91279137 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.194-9982_194-9981i others(20): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279137 | ||||||
| chr8:91279137 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01175.hp2 HG01515.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.194-9986_194-9985i others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279137 | ||||||
| chr8:91279137 | A | G | 5 | a0001c0001t0001g0010 a0001c0002t0001g0045 a0001c0002t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-9999A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279137 | |||||||
| chr8:91279139 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.194-9997A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279139 | |||||||
| chr8:91279153 | ATATATAT others(7): Show |
A | 4 | a0001c0001t0001g0101 a0001c0002t0001g0103 a0001c0002t0009g0102 others(1): Show |
4 | HG00735.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-9979_194-9966d others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279153 | ||||||
| chr8:91279155 | A | G | 11 | a0001c0001t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.194-9981A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279155 | |||||||
| chr8:91279155 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0105 a0001c0001t0023g0104 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.194-9977_194-9966d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91279155 | ||||||
| chr8:91279169 | A | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.194-9967A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279169 | |||||||
| chr8:91279371 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-9765A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279371 | |||||||
| chr8:91279646 | G | T | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-9490G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279646 | |||||||
| chr8:91279716 | C | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0196 others(3): Show |
7 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-9420C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279716 | |||||||
| chr8:91279721 | G | A | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.194-9415G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279721 | |||||||
| chr8:91279736 | T | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-9400T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279736 | |||||||
| chr8:91279795 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-9341G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91279795 | |||||||
| chr8:91280033 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
205 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.194-9103G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280033 | |||||||
| chr8:91280386 | C | T | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-8750C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280386 | |||||||
| chr8:91280523 | C | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-8613C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280523 | |||||||
| chr8:91280567 | C | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-8569C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280567 | |||||||
| chr8:91280641 | A | G | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-8495A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280641 | |||||||
| chr8:91280710 | T | A | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.194-8426T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280710 | |||||||
| chr8:91280784 | C | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG01978.hp1 HG02015.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-8352C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280784 | |||||||
| chr8:91280787 | C | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-8349C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91280787 | |||||||
| chr8:91281042 | A | G | 38 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0111 others(35): Show |
38 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.194-8094A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281042 | |||||||
| chr8:91281124 | C | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-8012C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281124 | |||||||
| chr8:91281192 | A | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-7944A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281192 | |||||||
| chr8:91281302 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-7834G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281302 | |||||||
| chr8:91281481 | C | T | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-7655C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281481 | |||||||
| chr8:91281482 | T | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-7654T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281482 | |||||||
| chr8:91281521 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-7615G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281521 | |||||||
| chr8:91281522 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-7614G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281522 | |||||||
| chr8:91281811 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-7325C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281811 | |||||||
| chr8:91281814 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0032 others(79): Show |
85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-7322G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281814 | |||||||
| chr8:91281876 | C | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0032 others(79): Show |
85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-7260C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91281876 | |||||||
| chr8:91282060 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-7076A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282060 | |||||||
| chr8:91282150 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.194-6986G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282150 | |||||||
| chr8:91282437 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-6699A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282437 | |||||||
| chr8:91282557 | A | T | 4 | a0001c0001t0001g0030 a0001c0002t0015g0024 a0001c0002t0022g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-6579A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282557 | |||||||
| chr8:91282692 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-6444T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282692 | |||||||
| chr8:91282841 | C | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-6295C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282841 | |||||||
| chr8:91282886 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-6250C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282886 | |||||||
| chr8:91282887 | C | T | 3 | a0001c0002t0001g0187 a0001c0002t0008g0189 a0001c0002t0008g0190 |
3 | HG00733.hp2 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.194-6249C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282887 | |||||||
| chr8:91282924 | TC | T | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-6211delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91282924 | |||||||
| chr8:91283657 | C | G | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.194-5479C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283657 | |||||||
| chr8:91283773 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.194-5363C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283773 | |||||||
| chr8:91283797 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-5339T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283797 | |||||||
| chr8:91283838 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-5298T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283838 | |||||||
| chr8:91283939 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-5197G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283939 | |||||||
| chr8:91283969 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-5167C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91283969 | |||||||
| chr8:91284045 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.194-5091T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284045 | |||||||
| chr8:91284100 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.194-5036G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284100 | |||||||
| chr8:91284119 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0032 others(79): Show |
85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-5017G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284119 | |||||||
| chr8:91284215 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-4921A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284215 | |||||||
| chr8:91284230 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4906A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284230 | |||||||
| chr8:91284322 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-4814G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284322 | |||||||
| chr8:91284377 | A | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-4759A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284377 | |||||||
| chr8:91284411 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0032 others(79): Show |
85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-4725A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284411 | |||||||
| chr8:91284483 | A | C | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4653A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284483 | |||||||
| chr8:91284537 | A | G | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4599A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284537 | |||||||
| chr8:91284651 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.194-4485A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284651 | |||||||
| chr8:91284664 | T | C | 3 | a0001c0001t0005g0004 a0001c0002t0002g0046 a0001c0002t0002g0047 |
3 | HG01070.hp2 HG01109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.194-4472T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284664 | |||||||
| chr8:91284670 | A | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.194-4466A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284670 | |||||||
| chr8:91284831 | G | T | 2 | a0002c0003t0001g0135 a0002c0003t0001g0136 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.194-4305G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91284831 | |||||||
| chr8:91285031 | A | C | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4105A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285031 | |||||||
| chr8:91285047 | A | T | 1 | a0002c0003t0004g0157 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.194-4089A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285047 | |||||||
| chr8:91285106 | G | T | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-4030G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285106 | |||||||
| chr8:91285159 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-3977T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285159 | |||||||
| chr8:91285211 | C | T | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.194-3925C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285211 | |||||||
| chr8:91285261 | G | A | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.194-3875G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285261 | |||||||
| chr8:91285309 | T | TTCA | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.194-3823_194-3821d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91285309 | ||||||
| chr8:91285358 | G | C | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.194-3778G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285358 | |||||||
| chr8:91285380 | C | A | 1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194-3756C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285380 | |||||||
| chr8:91285433 | G | A | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-3703G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91285433 | |||||||
| chr8:91286036 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.194-3100A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286036 | |||||||
| chr8:91286197 | G | A | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2939G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286197 | |||||||
| chr8:91286331 | G | A | 3 | a0001c0002t0015g0024 a0001c0002t0022g0023 a0004c0011t0014g0022 |
3 | HG01891.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.194-2805G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286331 | |||||||
| chr8:91286375 | A | G | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-2761A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286375 | |||||||
| chr8:91286466 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0032 others(79): Show |
85 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.194-2670T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286466 | |||||||
| chr8:91286515 | G | A | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.194-2621G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286515 | |||||||
| chr8:91286723 | G | A | 2 | a0001c0002t0002g0146 a0001c0002t0002g0147 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.194-2413G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286723 | |||||||
| chr8:91286866 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.194-2270A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91286866 | |||||||
| chr8:91287093 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0018g0124 |
4 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-2043T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287093 | |||||||
| chr8:91287633 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(140): Show |
146 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.194-1503T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287633 | |||||||
| chr8:91287879 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(66): Show |
71 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.194-1257C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287879 | |||||||
| chr8:91287939 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-1197C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91287939 | |||||||
| chr8:91288156 | T | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(119): Show |
125 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.194-980T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288156 | |||||||
| chr8:91288182 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.194-954C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288182 | |||||||
| chr8:91288285 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194-851G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288285 | |||||||
| chr8:91288601 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.194-535T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288601 | |||||||
| chr8:91288618 | C | CT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0032 others(83): Show |
89 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.194-517dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 91288618 | ||||||
| chr8:91288743 | C | G | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-393C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288743 | |||||||
| chr8:91288809 | A | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(66): Show |
71 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.194-327A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288809 | |||||||
| chr8:91288927 | A | T | 4 | a0001c0001t0001g0030 a0001c0002t0015g0024 a0001c0002t0022g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-209A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91288927 | |||||||
| chr8:91289021 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
72 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.194-115G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 2/18 | chr8 | 91289021 | |||||||
| chr8:91289727 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.304+481A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91289727 | |||||||
| chr8:91289928 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.304+682T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91289928 | |||||||
| chr8:91290306 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.304+1060C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290306 | |||||||
| chr8:91290570 | T | C | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.304+1324T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290570 | |||||||
| chr8:91290590 | G | A | 4 | a0001c0001t0001g0030 a0001c0002t0015g0024 a0001c0002t0022g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+1344G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290590 | |||||||
| chr8:91290636 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.304+1390T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290636 | |||||||
| chr8:91290953 | T | G | 32 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(29): Show |
32 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.304+1707T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91290953 | |||||||
| chr8:91291055 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.304+1809G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291055 | |||||||
| chr8:91291131 | A | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(140): Show |
146 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.304+1885A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291131 | |||||||
| chr8:91291205 | A | G | 2 | a0001c0001t0001g0119 a0001c0002t0002g0121 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.304+1959A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291205 | |||||||
| chr8:91291413 | G | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304+2167G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291413 | |||||||
| chr8:91291735 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.304+2489C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291735 | |||||||
| chr8:91291855 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.304+2609G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291855 | |||||||
| chr8:91291890 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(117): Show |
123 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.304+2644A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91291890 | |||||||
| chr8:91292001 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0196 others(6): Show |
10 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.304+2755G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292001 | |||||||
| chr8:91292090 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.304+2844G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292090 | |||||||
| chr8:91292112 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.304+2866T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292112 | |||||||
| chr8:91292291 | G | A | 1 | a0001c0001t0005g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.304+3045G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292291 | |||||||
| chr8:91292562 | T | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(7): Show |
10 | HG02257.hp2 HG02572.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.305-2969T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292562 | |||||||
| chr8:91292732 | G | GT | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-2789dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr8 | 91292732 | ||||||
| chr8:91292742 | T | A | 3 | a0001c0002t0015g0024 a0001c0002t0022g0023 a0004c0011t0014g0022 |
3 | HG01891.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.305-2789T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292742 | |||||||
| chr8:91292743 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0001t0018g0124 |
3 | HG01123.hp1 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.305-2788A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292743 | |||||||
| chr8:91292866 | A | G | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-2665A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91292866 | |||||||
| chr8:91293035 | A | G | 22 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(19): Show |
22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.305-2496A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293035 | |||||||
| chr8:91293050 | T | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | NA19010.hp2 NA19063.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.305-2481T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293050 | |||||||
| chr8:91293328 | C | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-2203C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293328 | |||||||
| chr8:91293689 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-1842C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293689 | |||||||
| chr8:91293798 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-1733T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293798 | |||||||
| chr8:91293885 | C | T | 1 | a0001c0001t0007g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.305-1646C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91293885 | |||||||
| chr8:91294012 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.305-1519A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294012 | |||||||
| chr8:91294161 | C | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0134 |
3 | HG02572.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.305-1370C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294161 | |||||||
| chr8:91294191 | T | C | 22 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0119 others(19): Show |
22 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.305-1340T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294191 | |||||||
| chr8:91294429 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-1102A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294429 | |||||||
| chr8:91294510 | G | A | 3 | a0001c0001t0001g0111 a0001c0002t0001g0110 a0001c0002t0001g0112 |
3 | HG01081.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.305-1021G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294510 | |||||||
| chr8:91294654 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.305-877G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294654 | |||||||
| chr8:91294743 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.305-788A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91294743 | |||||||
| chr8:91295006 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.305-525T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295006 | |||||||
| chr8:91295239 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.305-292C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295239 | |||||||
| chr8:91295357 | C | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.305-174C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295357 | |||||||
| chr8:91295373 | A | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.305-158A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295373 | |||||||
| chr8:91295386 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.305-145G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 3/18 | chr8 | 91295386 | |||||||
| chr8:91295750 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(94): Show |
100 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.477+47C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91295750 | |||||||
| chr8:91295900 | A | G | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.477+197A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91295900 | |||||||
| chr8:91296028 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0068 a0001c0001t0001g0145 others(4): Show |
7 | HG00609.hp1 HG02132.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+325C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296028 | |||||||
| chr8:91296029 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.477+326G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296029 | |||||||
| chr8:91296429 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.477+726G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296429 | |||||||
| chr8:91296509 | G | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+806G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296509 | |||||||
| chr8:91296629 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.477+926G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91296629 | |||||||
| chr8:91297204 | G | A | 1 | a0001c0004t0002g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.477+1501G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297204 | |||||||
| chr8:91297260 | C | T | 1 | a0001c0002t0003g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.477+1557C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297260 | |||||||
| chr8:91297540 | A | G | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.477+1837A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297540 | |||||||
| chr8:91297550 | A | T | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.477+1847A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91297550 | |||||||
| chr8:91298116 | C | T | 2 | a0001c0001t0001g0018 a0002c0003t0019g0009 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.477+2413C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91298116 | |||||||
| chr8:91298266 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
7 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+2563T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91298266 | |||||||
| chr8:91298471 | T | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.477+2768T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91298471 | |||||||
| chr8:91299016 | C | A | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.477+3313C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299016 | |||||||
| chr8:91299180 | T | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+3477T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299180 | |||||||
| chr8:91299184 | A | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.477+3481A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299184 | |||||||
| chr8:91299417 | T | TTTAAG | 69 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(66): Show |
69 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.477+3717_477+3718i others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91299417 | ||||||
| chr8:91299528 | T | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3825T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299528 | |||||||
| chr8:91299565 | T | TA | 4 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+3863dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91299565 | ||||||
| chr8:91299670 | A | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.477+3967A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299670 | |||||||
| chr8:91299981 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.477+4278T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91299981 | |||||||
| chr8:91300400 | AT | A | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+4712delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91300400 | ||||||
| chr8:91300437 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0162 |
2 | HG00438.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.477+4734A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300437 | |||||||
| chr8:91300447 | G | T | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.477+4744G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300447 | |||||||
| chr8:91300455 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0162 |
2 | HG00438.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.477+4752G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300455 | |||||||
| chr8:91300460 | C | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0162 |
2 | HG00438.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.477+4757C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300460 | |||||||
| chr8:91300466 | C | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0003t0004g0095 others(2): Show |
5 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+4763C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300466 | |||||||
| chr8:91300662 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.477+4959G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91300662 | |||||||
| chr8:91300928 | A | AT | 64 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(61): Show |
65 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.477+5229dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91300928 | ||||||
| chr8:91301154 | G | A | 16 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.477+5451G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301154 | |||||||
| chr8:91301800 | TTA | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0205 others(4): Show |
7 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+6099_477+6100d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91301800 | ||||||
| chr8:91301801 | TA | T | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+6099delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301801 | |||||||
| chr8:91301888 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.477+6185A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301888 | |||||||
| chr8:91301970 | T | C | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.477+6267T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91301970 | |||||||
| chr8:91302409 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+6706C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302409 | |||||||
| chr8:91302542 | G | A | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.477+6839G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302542 | |||||||
| chr8:91302818 | C | CTTTTTT | 20 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
20 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.477+7126_477+7131d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91302818 | ||||||
| chr8:91302818 | CT | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0030 others(98): Show |
103 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.477+7131delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91302818 | ||||||
| chr8:91302827 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.477+7124T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302827 | |||||||
| chr8:91302917 | C | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.477+7214C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302917 | |||||||
| chr8:91302948 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.477+7245G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91302948 | |||||||
| chr8:91303024 | G | A | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.477+7321G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303024 | |||||||
| chr8:91303219 | A | G | 8 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(5): Show |
8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+7516A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303219 | |||||||
| chr8:91303369 | C | T | 2 | a0001c0002t0015g0024 a0001c0002t0022g0023 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.477+7666C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303369 | |||||||
| chr8:91303393 | A | G | 13 | a0001c0001t0001g0119 a0001c0001t0005g0004 a0001c0001t0007g0005 others(10): Show |
13 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.477+7690A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303393 | |||||||
| chr8:91303701 | G | T | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+7998G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303701 | |||||||
| chr8:91303869 | CAGG | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.477+8174_477+8176d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91303869 | ||||||
| chr8:91303971 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+8268T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91303971 | |||||||
| chr8:91304114 | C | T | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.477+8411C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91304114 | |||||||
| chr8:91304403 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(46): Show |
50 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.477+8700A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91304403 | |||||||
| chr8:91304817 | T | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG01175.hp1 HG01192.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.477+9114T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91304817 | |||||||
| chr8:91305031 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.477+9328T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305031 | |||||||
| chr8:91305142 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.477+9439C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305142 | |||||||
| chr8:91305241 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.477+9538T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305241 | |||||||
| chr8:91305457 | C | A | 1 | a0001c0001t0005g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.477+9754C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305457 | |||||||
| chr8:91305581 | C | G | 16 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.477+9878C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91305581 | |||||||
| chr8:91305614 | A | AGCATCAG others(2): Show |
5 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(2): Show |
5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+9914_477+9922d others(11): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91305614 | ||||||
| chr8:91305742 | TTAGA | T | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.477+10044_477+1004 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91305742 | ||||||
| chr8:91306281 | A | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+10578A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306281 | |||||||
| chr8:91306294 | G | A | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.477+10591G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306294 | |||||||
| chr8:91306357 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.477+10654C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306357 | |||||||
| chr8:91306370 | GC | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0184 |
2 | HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.477+10668delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306370 | |||||||
| chr8:91306484 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+10781A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306484 | |||||||
| chr8:91306523 | A | G | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.477+10820A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306523 | |||||||
| chr8:91306569 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.477+10866A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306569 | |||||||
| chr8:91306665 | T | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(49): Show |
53 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.477+10962T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306665 | |||||||
| chr8:91306714 | AT | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(27): Show |
30 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.477+11024delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91306714 | ||||||
| chr8:91306788 | TAACCTGG others(3): Show |
T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.477+11086_477+1109 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306788 | |||||||
| chr8:91306923 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.477+11220A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306923 | |||||||
| chr8:91306969 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.478-11247C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91306969 | |||||||
| chr8:91307126 | G | A | 1 | a0001c0002t0003g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.478-11090G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307126 | |||||||
| chr8:91307332 | A | G | 4 | a0001c0001t0001g0013 a0001c0002t0003g0017 a0001c0002t0003g0020 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-10884A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307332 | |||||||
| chr8:91307409 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.478-10807A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307409 | |||||||
| chr8:91307444 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0090 |
2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.478-10772A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307444 | |||||||
| chr8:91307458 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.478-10758A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307458 | |||||||
| chr8:91307477 | T | G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-10739T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307477 | |||||||
| chr8:91307591 | T | C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(5): Show |
8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-10625T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307591 | |||||||
| chr8:91307660 | G | T | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-10556G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307660 | |||||||
| chr8:91307722 | C | T | 5 | a0001c0001t0001g0137 a0001c0002t0001g0014 a0001c0002t0001g0015 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-10494C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307722 | |||||||
| chr8:91307746 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(127): Show |
133 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.478-10470A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307746 | |||||||
| chr8:91307816 | T | TA | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
166 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.478-10392dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91307816 | ||||||
| chr8:91307833 | TTAAAA | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-10366_478-1036 others(9): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91307833 | ||||||
| chr8:91307872 | A | AT | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-10337dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91307872 | ||||||
| chr8:91307891 | G | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0119 others(16): Show |
20 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-10325G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307891 | |||||||
| chr8:91307899 | A | G | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.478-10317A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91307899 | |||||||
| chr8:91308246 | G | GGT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0058 others(20): Show |
24 | HG01175.hp2 HG01261.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.478-9937_478-9936d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | ||||||
| chr8:91308246 | G | GGTGT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0122 others(8): Show |
12 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478-9939_478-9936d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | ||||||
| chr8:91308246 | GGT | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0079 others(7): Show |
10 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-9937_478-9936d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | ||||||
| chr8:91308246 | GGTGT | G | 11 | a0001c0001t0001g0081 a0001c0001t0001g0111 a0001c0001t0002g0063 others(8): Show |
11 | HG00558.hp2 HG01070.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-9939_478-9936d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308246 | ||||||
| chr8:91308393 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.478-9823G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308393 | |||||||
| chr8:91308412 | C | CT | 57 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
58 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.478-9801dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91308412 | ||||||
| chr8:91308518 | T | C | 1 | a0001c0002t0002g0148 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.478-9698T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308518 | |||||||
| chr8:91308562 | A | C | 2 | a0001c0001t0001g0173 a0001c0001t0002g0063 |
2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.478-9654A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308562 | |||||||
| chr8:91308564 | A | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-9652A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308564 | |||||||
| chr8:91308569 | A | G | 2 | a0001c0001t0004g0202 a0001c0001t0012g0117 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.478-9647A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308569 | |||||||
| chr8:91308688 | C | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-9528C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91308688 | |||||||
| chr8:91309012 | T | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-9204T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309012 | |||||||
| chr8:91309247 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.478-8969T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309247 | |||||||
| chr8:91309506 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.478-8710A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309506 | |||||||
| chr8:91309885 | G | A | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478-8331G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309885 | |||||||
| chr8:91309897 | A | G | 5 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0002c0003t0004g0095 others(2): Show |
5 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-8319A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309897 | |||||||
| chr8:91309915 | T | G | 8 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(5): Show |
8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-8301T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91309915 | |||||||
| chr8:91310145 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.478-8071C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310145 | |||||||
| chr8:91310259 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.478-7957A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310259 | |||||||
| chr8:91310549 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.478-7667G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310549 | |||||||
| chr8:91310683 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0096 |
2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.478-7533G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310683 | |||||||
| chr8:91310816 | G | T | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-7400G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310816 | |||||||
| chr8:91310851 | C | CA | 58 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
59 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.478-7362dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91310851 | ||||||
| chr8:91310991 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.478-7225C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91310991 | |||||||
| chr8:91311115 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.478-7101A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311115 | |||||||
| chr8:91311229 | G | T | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.478-6987G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311229 | |||||||
| chr8:91311275 | A | G | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478-6941A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311275 | |||||||
| chr8:91311391 | G | A | 2 | a0001c0002t0002g0146 a0001c0002t0002g0147 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.478-6825G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311391 | |||||||
| chr8:91311431 | TTATATA | T | 2 | a0001c0001t0001g0205 a0001c0001t0021g0206 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.478-6778_478-6773d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91311431 | ||||||
| chr8:91311448 | C | T | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.478-6768C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311448 | |||||||
| chr8:91311596 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(65): Show |
70 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.478-6620C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311596 | |||||||
| chr8:91311722 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-6494G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91311722 | |||||||
| chr8:91312056 | C | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-6160C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312056 | |||||||
| chr8:91312262 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.478-5954C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312262 | |||||||
| chr8:91312273 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478-5943A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312273 | |||||||
| chr8:91312370 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.478-5846T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312370 | |||||||
| chr8:91312379 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.478-5837A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312379 | |||||||
| chr8:91312380 | T | C | 3 | a0001c0001t0007g0005 a0001c0001t0007g0006 a0001c0001t0007g0120 |
3 | HG00558.hp2 NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.478-5836T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312380 | |||||||
| chr8:91312560 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.478-5656T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312560 | |||||||
| chr8:91312641 | C | CTG | 2 | a0001c0001t0001g0105 a0001c0001t0023g0104 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.478-5543_478-5542d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312641 | C | CTGTG | 5 | a0001c0001t0001g0101 a0001c0001t0005g0099 a0001c0002t0001g0103 others(2): Show |
5 | HG00735.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-5545_478-5542d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312641 | CTG | C | 50 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(47): Show |
51 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.478-5543_478-5542d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312641 | CTGTG | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(76): Show |
80 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.478-5545_478-5542d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312641 | CTGTGTG | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0025 others(56): Show |
60 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.478-5547_478-5542d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312641 | CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0096 a0001c0002t0003g0204 |
3 | HG00639.hp2 HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.478-5549_478-5542d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312641 | CTGTGTGT others(3): Show |
C | 1 | a0001c0002t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.478-5551_478-5542d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91312641 | ||||||
| chr8:91312713 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0193 |
2 | HG03017.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.478-5503C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312713 | |||||||
| chr8:91312864 | A | T | 17 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-5352A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312864 | |||||||
| chr8:91312917 | A | T | 2 | a0001c0002t0001g0197 a0001c0002t0002g0029 |
2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.478-5299A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312917 | |||||||
| chr8:91312966 | C | G | 5 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(2): Show |
5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-5250C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91312966 | |||||||
| chr8:91313043 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0191 others(1): Show |
4 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-5173A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313043 | |||||||
| chr8:91313515 | A | G | 19 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(16): Show |
19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.478-4701A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313515 | |||||||
| chr8:91313685 | A | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0032 others(70): Show |
75 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.478-4531A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313685 | |||||||
| chr8:91313696 | C | T | 2 | a0001c0001t0001g0002 a0004c0011t0014g0022 |
3 | HG01891.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.478-4520C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313696 | |||||||
| chr8:91313873 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.478-4343C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91313873 | |||||||
| chr8:91314389 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-3827A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314389 | |||||||
| chr8:91314461 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.478-3755G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314461 | |||||||
| chr8:91314635 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.478-3581T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314635 | |||||||
| chr8:91314736 | C | T | 17 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-3480C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314736 | |||||||
| chr8:91314765 | T | A | 19 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(16): Show |
19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.478-3451T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314765 | |||||||
| chr8:91314859 | G | C | 5 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(2): Show |
5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-3357G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314859 | |||||||
| chr8:91314931 | T | G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-3285T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91314931 | |||||||
| chr8:91315164 | C | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-3052C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315164 | |||||||
| chr8:91315200 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.478-3016T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315200 | |||||||
| chr8:91315291 | A | C | 17 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-2925A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315291 | |||||||
| chr8:91315326 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0096 |
2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.478-2890G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315326 | |||||||
| chr8:91315456 | C | CA | 32 | a0001c0001t0001g0030 a0001c0001t0001g0048 a0001c0001t0001g0052 others(29): Show |
32 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.478-2745dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91315456 | ||||||
| chr8:91315471 | A | AAT | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-2745_478-2744i others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315471 | |||||||
| chr8:91315471 | A | AT | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-2745_478-2744i others(3): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315471 | |||||||
| chr8:91315591 | C | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-2625C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315591 | |||||||
| chr8:91315598 | T | G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-2618T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315598 | |||||||
| chr8:91315758 | C | G | 1 | a0001c0007t0002g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.478-2458C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315758 | |||||||
| chr8:91315790 | T | A | 1 | a0001c0002t0002g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.478-2426T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91315790 | |||||||
| chr8:91316046 | G | A | 6 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0009g0201 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-2170G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316046 | |||||||
| chr8:91316058 | C | T | 17 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-2158C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316058 | |||||||
| chr8:91316222 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.478-1994C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316222 | |||||||
| chr8:91316223 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02615.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.478-1993G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316223 | |||||||
| chr8:91316370 | C | T | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478-1846C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316370 | |||||||
| chr8:91316451 | A | AT | 7 | a0001c0001t0001g0028 a0001c0001t0001g0142 a0001c0001t0001g0169 others(4): Show |
7 | HG01069.hp1 HG01256.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1726dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | A | ATT | 11 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0097 others(8): Show |
11 | HG00642.hp2 HG00733.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-1727_478-1726d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | AT | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0128 others(9): Show |
13 | HG01175.hp1 HG01175.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-1726delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATT | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0129 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.478-1727_478-1726d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTT | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(23): Show |
26 | HG00609.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.478-1728_478-1726d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTT | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0049 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-1729_478-1726d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTT | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0035 others(38): Show |
43 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.478-1730_478-1726d others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTT | A | 33 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0039 others(30): Show |
33 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.478-1731_478-1726d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0003g0113 others(1): Show |
4 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-1737_478-1726d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.478-1738_478-1726d others(15): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTTT others(9): Show |
A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0199 a0001c0002t0001g0112 others(1): Show |
4 | HG01433.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1741_478-1726d others(18): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTTT others(10): Show |
A | 14 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0005g0004 others(11): Show |
14 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-1742_478-1726d others(19): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.478-1743_478-1726d others(20): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316451 | ATTTTTTT others(12): Show |
A | 2 | a0001c0002t0001g0045 a0001c0008t0001g0031 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.478-1744_478-1726d others(21): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316451 | ||||||
| chr8:91316471 | T | C | 1 | a0001c0008t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.478-1745T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316471 | |||||||
| chr8:91316725 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.478-1491A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316725 | |||||||
| chr8:91316806 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0173 a0001c0001t0002g0063 |
3 | HG01993.hp2 HG02300.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.478-1410G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316806 | |||||||
| chr8:91316965 | G | A | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1251G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91316965 | |||||||
| chr8:91316988 | T | TA | 15 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0001g0084 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.478-1195dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | T | TAAAAAAA | 6 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0137 others(3): Show |
6 | HG01069.hp1 HG01081.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1201_478-1195d others(9): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | T | TAAAAAAA others(1): Show |
9 | a0001c0001t0001g0026 a0001c0001t0001g0073 a0001c0001t0001g0096 others(6): Show |
9 | HG00639.hp2 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-1202_478-1195d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0097 a0001c0002t0001g0187 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.478-1204_478-1195d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | T | TAAAAAAA others(4): Show |
1 | a0001c0002t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.478-1205_478-1195d others(13): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | TA | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0033 others(84): Show |
89 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.478-1195delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | TAA | T | 18 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0111 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.478-1196_478-1195d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91316988 | TAAAAAAA others(12): Show |
T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-1213_478-1195d others(21): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91316988 | ||||||
| chr8:91317178 | A | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-1038A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317178 | |||||||
| chr8:91317360 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-856C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317360 | |||||||
| chr8:91317426 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.478-790T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317426 | |||||||
| chr8:91317939 | GAT | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(124): Show |
128 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.478-259_478-258del others(2): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91317939 | ||||||
| chr8:91317939 | GATAT | G | 2 | a0001c0001t0001g0097 a0001c0002t0003g0204 |
2 | HG00642.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.478-261_478-258del others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr8 | 91317939 | ||||||
| chr8:91317944 | A | C | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.478-272A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317944 | |||||||
| chr8:91317956 | A | AAAAT | 4 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0002g0001 others(1): Show |
5 | HG02622.hp2 HG03195.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-260_478-259ins others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317956 | |||||||
| chr8:91317957 | T | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0002g0001 others(1): Show |
5 | HG02622.hp2 HG03195.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-259T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317957 | |||||||
| chr8:91317987 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0002g0139 |
2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.478-229T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317987 | |||||||
| chr8:91317993 | A | T | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 |
3 | HG01256.hp1 HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.478-223A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91317993 | |||||||
| chr8:91318005 | A | AG | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-211_478-210ins others(1): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91318005 | |||||||
| chr8:91318189 | C | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.478-27C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 4/18 | chr8 | 91318189 | |||||||
| chr8:91318473 | A | G | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.642+93A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91318473 | |||||||
| chr8:91318839 | A | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(45): Show |
48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+459A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91318839 | |||||||
| chr8:91318980 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(45): Show |
48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+600C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91318980 | |||||||
| chr8:91319073 | G | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.642+693G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319073 | |||||||
| chr8:91319174 | T | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(45): Show |
48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+794T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319174 | |||||||
| chr8:91319223 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642+843T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319223 | |||||||
| chr8:91319662 | T | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+1282T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319662 | |||||||
| chr8:91319805 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.642+1425A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91319805 | |||||||
| chr8:91319965 | A | AG | 48 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(45): Show |
48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+1587dupG | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91319965 | ||||||
| chr8:91320049 | T | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.642+1669T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91320049 | |||||||
| chr8:91320537 | C | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+2157C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91320537 | |||||||
| chr8:91321193 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.642+2813T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321193 | |||||||
| chr8:91321227 | A | G | 2 | a0001c0001t0001g0003 a0001c0002t0001g0198 |
3 | HG00738.hp2 HG01192.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.642+2847A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321227 | |||||||
| chr8:91321245 | G | A | 1 | a0001c0002t0008g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.642+2865G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321245 | |||||||
| chr8:91321418 | G | C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(5): Show |
8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+3038G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321418 | |||||||
| chr8:91321908 | CT | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0032 others(71): Show |
76 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.642+3529delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91321908 | |||||||
| chr8:91322158 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(45): Show |
48 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+3778C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322158 | |||||||
| chr8:91322205 | C | CTTCT | 2 | a0001c0001t0001g0002 a0001c0002t0003g0204 |
3 | HG02896.hp1 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.642+3826_642+3829d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91322205 | ||||||
| chr8:91322417 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+4037G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322417 | |||||||
| chr8:91322429 | T | G | 2 | a0002c0003t0001g0135 a0002c0003t0001g0136 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.642+4049T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322429 | |||||||
| chr8:91322823 | G | T | 1 | a0001c0001t0004g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642+4443G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322823 | |||||||
| chr8:91322824 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642+4444C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322824 | |||||||
| chr8:91322948 | A | G | 8 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(5): Show |
8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+4568A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91322948 | |||||||
| chr8:91323174 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(55): Show |
59 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.642+4794T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323174 | |||||||
| chr8:91323411 | A | G | 19 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(16): Show |
19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+5031A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323411 | |||||||
| chr8:91323444 | C | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+5064C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323444 | |||||||
| chr8:91323461 | A | G | 8 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(5): Show |
8 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+5081A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323461 | |||||||
| chr8:91323627 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.642+5247C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323627 | |||||||
| chr8:91323818 | C | CT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0105 others(9): Show |
12 | HG00735.hp1 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.642+5456dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | ||||||
| chr8:91323818 | C | CTT | 26 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(23): Show |
26 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.642+5455_642+5456d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | ||||||
| chr8:91323818 | CT | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0033 others(68): Show |
73 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.642+5456delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | ||||||
| chr8:91323818 | CTT | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+5455_642+5456d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | ||||||
| chr8:91323818 | CTTTTTTT others(1): Show |
C | 19 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(16): Show |
19 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+5449_642+5456d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91323818 | ||||||
| chr8:91323843 | T | C | 5 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(2): Show |
5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+5463T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91323843 | |||||||
| chr8:91324058 | G | A | 57 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(54): Show |
57 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.642+5678G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91324058 | |||||||
| chr8:91324271 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.642+5891T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91324271 | |||||||
| chr8:91324435 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.642+6055G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91324435 | |||||||
| chr8:91325235 | G | A | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.642+6855G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325235 | |||||||
| chr8:91325283 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02155.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.642+6903T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325283 | |||||||
| chr8:91325416 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.642+7036C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325416 | |||||||
| chr8:91325483 | G | A | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.642+7103G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325483 | |||||||
| chr8:91325647 | C | A | 18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(15): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+7267C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325647 | |||||||
| chr8:91325694 | C | T | 1 | a0001c0001t0021g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.642+7314C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91325694 | |||||||
| chr8:91326164 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.642+7784T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326164 | |||||||
| chr8:91326284 | A | G | 4 | a0001c0001t0001g0013 a0001c0002t0003g0017 a0001c0002t0003g0020 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+7904A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326284 | |||||||
| chr8:91326422 | T | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-7873T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326422 | |||||||
| chr8:91326856 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.643-7439C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326856 | |||||||
| chr8:91326895 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.643-7400C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326895 | |||||||
| chr8:91326908 | C | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0085 others(12): Show |
16 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-7387C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91326908 | |||||||
| chr8:91327022 | G | A | 56 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(53): Show |
56 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.643-7273G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327022 | |||||||
| chr8:91327045 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.643-7250C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327045 | |||||||
| chr8:91327046 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.643-7249T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327046 | |||||||
| chr8:91327136 | G | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-7159G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327136 | |||||||
| chr8:91327162 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(42): Show |
45 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.643-7133C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327162 | |||||||
| chr8:91327173 | A | T | 4 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(1): Show |
4 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-7122A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327173 | |||||||
| chr8:91327321 | C | T | 1 | a0001c0008t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.643-6974C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327321 | |||||||
| chr8:91327419 | A | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-6876A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327419 | |||||||
| chr8:91327550 | A | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-6745A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327550 | |||||||
| chr8:91327627 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.643-6668G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327627 | |||||||
| chr8:91327907 | G | A | 57 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(54): Show |
57 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.643-6388G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91327907 | |||||||
| chr8:91328021 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.643-6274A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91328021 | |||||||
| chr8:91328116 | T | A | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.643-6179T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91328116 | |||||||
| chr8:91328762 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0196 others(3): Show |
7 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-5533G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91328762 | |||||||
| chr8:91329145 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0098 |
2 | HG00558.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.643-5150G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329145 | |||||||
| chr8:91329234 | A | ATGTGTG | 47 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(44): Show |
47 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.643-5056_643-5051d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91329234 | ||||||
| chr8:91329298 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.643-4997C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329298 | |||||||
| chr8:91329419 | G | A | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.643-4876G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329419 | |||||||
| chr8:91329449 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
22 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.643-4846C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329449 | |||||||
| chr8:91329484 | T | C | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-4811T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329484 | |||||||
| chr8:91329741 | C | A | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-4554C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329741 | |||||||
| chr8:91329840 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0101 a0001c0001t0001g0105 others(6): Show |
10 | HG00735.hp1 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-4455T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329840 | |||||||
| chr8:91329874 | T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.643-4421T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91329874 | |||||||
| chr8:91330037 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(58): Show |
62 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.643-4258G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330037 | |||||||
| chr8:91330055 | A | G | 47 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0025 others(44): Show |
47 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.643-4240A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330055 | |||||||
| chr8:91330081 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.643-4214G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330081 | |||||||
| chr8:91330165 | T | C | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.643-4130T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330165 | |||||||
| chr8:91330290 | G | A | 1 | a0002c0003t0019g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.643-4005G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330290 | |||||||
| chr8:91330397 | A | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0009g0201 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-3898A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330397 | |||||||
| chr8:91330494 | A | G | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-3801A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330494 | |||||||
| chr8:91330498 | T | C | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02818.hp2 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-3797T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330498 | |||||||
| chr8:91330501 | T | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.643-3794T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330501 | |||||||
| chr8:91330713 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG00741.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.643-3582C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330713 | |||||||
| chr8:91330716 | A | G | 10 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0105 others(7): Show |
10 | HG00735.hp1 HG01261.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-3579A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91330716 | |||||||
| chr8:91331808 | A | T | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-2487A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91331808 | |||||||
| chr8:91331910 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0081 others(3): Show |
6 | HG01981.hp2 HG01993.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-2385A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91331910 | |||||||
| chr8:91332103 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.643-2192G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332103 | |||||||
| chr8:91332144 | C | CAT | 14 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0114 others(11): Show |
14 | HG00735.hp1 HG01243.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-2137_643-2136d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332144 | ||||||
| chr8:91332227 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0018g0124 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.643-2068A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332227 | |||||||
| chr8:91332250 | A | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.643-2045A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332250 | |||||||
| chr8:91332351 | A | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0101 a0001c0001t0001g0105 others(5): Show |
9 | HG00735.hp1 HG02486.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-1944A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332351 | |||||||
| chr8:91332370 | A | G | 5 | a0001c0001t0005g0108 a0001c0002t0001g0107 a0001c0005t0006g0106 others(2): Show |
5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1925A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332370 | |||||||
| chr8:91332395 | T | TTATATTT others(27): Show |
18 | a0001c0001t0001g0111 a0001c0001t0001g0119 a0001c0001t0001g0199 others(15): Show |
18 | HG00741.hp1 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-1887_643-1854d others(36): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332395 | ||||||
| chr8:91332491 | T | TAC | 32 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0050 others(29): Show |
33 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.643-1762_643-1761d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | T | TACAC | 47 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0040 others(44): Show |
47 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.643-1764_643-1761d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | T | TACACAC | 12 | a0001c0001t0001g0043 a0001c0001t0001g0126 a0001c0001t0001g0128 others(9): Show |
12 | HG00609.hp1 HG00741.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.643-1766_643-1761d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0002t0002g0121 others(3): Show |
6 | HG02630.hp2 HG02895.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-1768_643-1761d others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | T | TACACACA others(3): Show |
5 | a0001c0001t0001g0134 a0001c0001t0005g0108 a0001c0002t0001g0107 others(2): Show |
5 | HG02970.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1770_643-1761d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | TAC | T | 22 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0056 others(19): Show |
22 | HG00609.hp2 HG00642.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.643-1762_643-1761d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | TACAC | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0091 a0001c0001t0001g0140 others(4): Show |
7 | HG00280.hp2 HG00733.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1764_643-1761d others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | TACACAC | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0127 |
3 | HG00438.hp2 HG01261.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.643-1766_643-1761d others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.643-1770_643-1761d others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332491 | TACACACA others(5): Show |
T | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1772_643-1761d others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332491 | ||||||
| chr8:91332697 | A | AT | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0005g0099 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1592dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 91332697 | ||||||
| chr8:91332769 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.643-1526C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332769 | |||||||
| chr8:91332770 | G | C | 1 | a0001c0002t0003g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-1525G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332770 | |||||||
| chr8:91332776 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01175.hp2 HG01515.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1519T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332776 | |||||||
| chr8:91332965 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0127 |
2 | HG01261.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.643-1330C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91332965 | |||||||
| chr8:91333373 | A | G | 113 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0032 others(110): Show |
114 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.643-922A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333373 | |||||||
| chr8:91333519 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(157): Show |
163 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.643-776A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333519 | |||||||
| chr8:91333537 | C | T | 1 | a0001c0012t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.643-758C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333537 | |||||||
| chr8:91333616 | TC | T | 2 | a0001c0001t0001g0105 a0001c0001t0023g0104 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.643-678delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333616 | |||||||
| chr8:91333772 | A | G | 1 | a0001c0002t0008g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.643-523A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333772 | |||||||
| chr8:91333959 | G | T | 1 | a0001c0002t0002g0046 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.643-336G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91333959 | |||||||
| chr8:91334234 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.643-61T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 5/18 | chr8 | 91334234 | |||||||
| chr8:91334620 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.795+173A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334620 | |||||||
| chr8:91334671 | T | C | 1 | a0001c0002t0012g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.795+224T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334671 | |||||||
| chr8:91334710 | T | C | 3 | a0001c0001t0001g0199 a0001c0002t0001g0110 a0001c0002t0001g0112 |
3 | HG02486.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.795+263T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334710 | |||||||
| chr8:91334993 | A | C | 13 | a0001c0001t0001g0199 a0001c0002t0001g0045 a0001c0002t0001g0110 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.795+546A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91334993 | |||||||
| chr8:91335213 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.795+766T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335213 | |||||||
| chr8:91335305 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(125): Show |
131 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.795+858C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335305 | |||||||
| chr8:91335354 | T | C | 2 | a0001c0002t0008g0189 a0001c0002t0008g0190 |
2 | HG00733.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.795+907T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335354 | |||||||
| chr8:91335385 | A | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0055 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.795+938A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335385 | |||||||
| chr8:91335704 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.795+1257A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335704 | |||||||
| chr8:91335798 | A | G | 22 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(19): Show |
22 | HG00733.hp2 HG01074.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.795+1351A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335798 | |||||||
| chr8:91335843 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.795+1396T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335843 | |||||||
| chr8:91335903 | T | G | 3 | a0002c0003t0004g0095 a0002c0003t0004g0156 a0002c0003t0004g0157 |
3 | HG00642.hp1 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.795+1456T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91335903 | |||||||
| chr8:91336004 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(29): Show |
34 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.795+1557C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336004 | |||||||
| chr8:91336023 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.795+1576C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336023 | |||||||
| chr8:91336064 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.795+1617A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336064 | |||||||
| chr8:91336338 | G | A | 6 | a0001c0001t0005g0099 a0001c0002t0001g0103 a0001c0002t0009g0102 others(3): Show |
6 | HG00735.hp1 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-1812G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336338 | |||||||
| chr8:91336401 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0137 others(4): Show |
7 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1749C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336401 | |||||||
| chr8:91336419 | T | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(139): Show |
145 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.796-1731T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336419 | |||||||
| chr8:91336454 | G | C | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.796-1696G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336454 | |||||||
| chr8:91336558 | A | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(69): Show |
73 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.796-1592A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336558 | |||||||
| chr8:91336607 | A | C | 22 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(19): Show |
22 | HG00733.hp2 HG01074.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.796-1543A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336607 | |||||||
| chr8:91336670 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0119 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.796-1480G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336670 | |||||||
| chr8:91336745 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(29): Show |
34 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.796-1405G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91336745 | |||||||
| chr8:91337145 | CT | C | 19 | a0001c0001t0001g0199 a0001c0001t0005g0099 a0001c0002t0001g0045 others(16): Show |
19 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.796-1004delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91337145 | |||||||
| chr8:91337661 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
132 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.796-489T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | chr8 | 91337661 | |||||||
| chr8:91337955 | CT | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
132 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.796-193delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 91337955 | ||||||
| chr8:91338339 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.878+107T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338339 | |||||||
| chr8:91338456 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(51): Show |
56 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.878+224G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338456 | |||||||
| chr8:91338700 | C | T | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.878+468C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338700 | |||||||
| chr8:91338741 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0023g0104 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.878+509G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338741 | |||||||
| chr8:91338769 | A | G | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.878+537A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338769 | |||||||
| chr8:91338962 | A | G | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.878+730A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338962 | |||||||
| chr8:91338976 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(68): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.878+744G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91338976 | |||||||
| chr8:91339137 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.878+905T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339137 | |||||||
| chr8:91339264 | C | T | 1 | a0001c0001t0021g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.878+1032C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339264 | |||||||
| chr8:91339355 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.879-1049C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339355 | |||||||
| chr8:91339407 | G | T | 19 | a0001c0001t0001g0199 a0001c0001t0005g0099 a0001c0002t0001g0045 others(16): Show |
19 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.879-997G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339407 | |||||||
| chr8:91339423 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(68): Show |
72 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.879-981A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339423 | |||||||
| chr8:91339627 | G | GATTT | 53 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0101 others(50): Show |
53 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.879-743_879-740dup others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339627 | G | GATTTATT others(1): Show |
8 | a0001c0002t0001g0045 a0001c0002t0002g0047 a0001c0002t0003g0011 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.879-747_879-740dup others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339627 | G | GATTTATT others(5): Show |
2 | a0001c0001t0001g0199 a0001c0002t0001g0112 |
2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.879-751_879-740dup others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339627 | G | GATTTATT others(9): Show |
1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879-755_879-740dup others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339627 | GATTT | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.879-743_879-740del others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339627 | GATTTATT others(1): Show |
G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0122 others(12): Show |
17 | HG01123.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.879-747_879-740del others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339627 | GATTTATT others(9): Show |
G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0064 others(2): Show |
5 | HG02132.hp2 NA18989.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.879-755_879-740del others(16): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr8 | 91339627 | ||||||
| chr8:91339773 | T | C | 6 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(3): Show |
6 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-631T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91339773 | |||||||
| chr8:91340244 | A | G | 6 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(3): Show |
6 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-160A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91340244 | |||||||
| chr8:91340325 | G | A | 6 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(3): Show |
6 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-79G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91340325 | |||||||
| chr8:91340385 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0127 a0001c0001t0004g0202 |
3 | HG01261.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.879-19A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 7/18 | chr8 | 91340385 | |||||||
| chr8:91340659 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(138): Show |
144 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(141): Show |
intron_variant | MODIFIER | c.1026+108C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91340659 | |||||||
| chr8:91340988 | CT | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(76): Show |
80 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1026+450delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 91340988 | ||||||
| chr8:91341048 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0023g0104 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1026+497A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341048 | |||||||
| chr8:91341076 | C | A | 1 | a0001c0001t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1026+525C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341076 | |||||||
| chr8:91341510 | C | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0168 |
2 | HG00558.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.1026+959C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341510 | |||||||
| chr8:91341670 | C | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(51): Show |
56 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1026+1119C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341670 | |||||||
| chr8:91341740 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(10): Show |
15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026+1189A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341740 | |||||||
| chr8:91341965 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1027-1388G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91341965 | |||||||
| chr8:91342039 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1027-1314C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342039 | |||||||
| chr8:91342094 | C | CT | 10 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0060 others(7): Show |
10 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-1249dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 91342094 | ||||||
| chr8:91342115 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1027-1238A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342115 | |||||||
| chr8:91342130 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0066 |
2 | NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1027-1223T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342130 | |||||||
| chr8:91342445 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0085 others(4): Show |
7 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027-908G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342445 | |||||||
| chr8:91342656 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1027-697C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342656 | |||||||
| chr8:91342693 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(125): Show |
131 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.1027-660G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342693 | |||||||
| chr8:91342821 | C | T | 2 | a0001c0002t0003g0011 a0001c0002t0003g0204 |
2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1027-532C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91342821 | |||||||
| chr8:91343311 | A | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1027-42A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 8/18 | chr8 | 91343311 | |||||||
| chr8:91343808 | A | C | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1140+342A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91343808 | |||||||
| chr8:91344101 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1140+635T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344101 | |||||||
| chr8:91344137 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1140+671G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344137 | |||||||
| chr8:91344522 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0119 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1140+1056A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344522 | |||||||
| chr8:91344545 | G | A | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1140+1079G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344545 | |||||||
| chr8:91344977 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+1511C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91344977 | |||||||
| chr8:91345023 | GC | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0072 |
3 | HG03195.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1140+1559delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91345023 | ||||||
| chr8:91345107 | AT | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0040 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1140+1653delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91345107 | ||||||
| chr8:91345291 | A | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0137 others(4): Show |
7 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+1825A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345291 | |||||||
| chr8:91345512 | T | A | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1140+2046T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345512 | |||||||
| chr8:91345590 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1140+2124C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345590 | |||||||
| chr8:91345725 | G | C | 3 | a0001c0001t0001g0030 a0003c0009t0011g0138 a0004c0011t0014g0022 |
3 | HG01243.hp2 HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1140+2259G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345725 | |||||||
| chr8:91345763 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1140+2297G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345763 | |||||||
| chr8:91345820 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(10): Show |
15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1140+2354G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345820 | |||||||
| chr8:91345823 | A | C | 1 | a0001c0001t0005g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1140+2357A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345823 | |||||||
| chr8:91345889 | G | T | 6 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(3): Show |
6 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140+2423G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91345889 | |||||||
| chr8:91346246 | A | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0076 a0001c0001t0001g0085 others(4): Show |
7 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1140+2780A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346246 | |||||||
| chr8:91346344 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(5): Show |
10 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1140+2878C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346344 | |||||||
| chr8:91346501 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+3035T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346501 | |||||||
| chr8:91346531 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+3065G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346531 | |||||||
| chr8:91346545 | A | G | 13 | a0001c0001t0001g0199 a0001c0002t0001g0045 a0001c0002t0001g0110 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1140+3079A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346545 | |||||||
| chr8:91346842 | A | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1140+3376A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346842 | |||||||
| chr8:91346955 | C | T | 1 | a0001c0001t0020g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1140+3489C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346955 | |||||||
| chr8:91346982 | G | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
71 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1140+3516G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91346982 | |||||||
| chr8:91347109 | G | A | 6 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(3): Show |
6 | HG00642.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140+3643G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347109 | |||||||
| chr8:91347265 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1140+3799A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347265 | |||||||
| chr8:91347320 | G | A | 1 | a0005c0010t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1140+3854G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347320 | |||||||
| chr8:91347339 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1140+3873A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347339 | |||||||
| chr8:91347536 | T | C | 22 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(19): Show |
22 | HG00733.hp2 HG01074.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1140+4070T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347536 | |||||||
| chr8:91347725 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0021g0206 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1141-4085A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347725 | |||||||
| chr8:91347877 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1141-3933C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347877 | |||||||
| chr8:91347922 | C | T | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1141-3888C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347922 | |||||||
| chr8:91347965 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
85 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.1141-3845T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91347965 | |||||||
| chr8:91348005 | G | A | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1141-3805G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348005 | |||||||
| chr8:91348086 | A | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1141-3724A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348086 | |||||||
| chr8:91348138 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0119 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1141-3672A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348138 | |||||||
| chr8:91348168 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(43): Show |
48 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1141-3642T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348168 | |||||||
| chr8:91348348 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(62): Show |
67 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1141-3462G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348348 | |||||||
| chr8:91348389 | G | A | 18 | a0001c0002t0001g0045 a0001c0002t0001g0103 a0001c0002t0001g0110 others(15): Show |
18 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1141-3421G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348389 | |||||||
| chr8:91348492 | A | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0119 others(12): Show |
17 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1141-3318A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348492 | |||||||
| chr8:91348602 | T | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0097 a0001c0001t0001g0153 |
3 | HG00639.hp1 HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1141-3208T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348602 | |||||||
| chr8:91348719 | TC | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(71): Show |
76 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1141-3089delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91348719 | ||||||
| chr8:91348720 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-3090C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348720 | |||||||
| chr8:91348978 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(64): Show |
69 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1141-2832G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91348978 | |||||||
| chr8:91349011 | A | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-2799A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349011 | |||||||
| chr8:91349054 | T | C | 1 | a0001c0002t0006g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1141-2756T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349054 | |||||||
| chr8:91349173 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-2637G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349173 | |||||||
| chr8:91349240 | AC | A | 23 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(20): Show |
23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1141-2567delC | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91349240 | ||||||
| chr8:91349285 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1141-2525G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349285 | |||||||
| chr8:91349569 | C | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-2241C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91349569 | |||||||
| chr8:91350002 | T | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1141-1808T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350002 | |||||||
| chr8:91350347 | CT | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0170 others(2): Show |
5 | HG01069.hp1 HG01255.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1452delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91350347 | ||||||
| chr8:91350359 | A | T | 9 | a0001c0001t0005g0004 a0001c0001t0005g0099 a0001c0001t0005g0118 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-1451A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350359 | |||||||
| chr8:91350439 | GA | G | 42 | a0001c0002t0001g0027 a0001c0002t0001g0045 a0001c0002t0001g0053 others(39): Show |
42 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1141-1362delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 91350439 | ||||||
| chr8:91350559 | C | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1141-1251C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350559 | |||||||
| chr8:91350677 | G | A | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1141-1133G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350677 | |||||||
| chr8:91350799 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1141-1011G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350799 | |||||||
| chr8:91350836 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1141-974T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91350836 | |||||||
| chr8:91351162 | A | G | 47 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1141-648A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351162 | |||||||
| chr8:91351279 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1141-531G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351279 | |||||||
| chr8:91351290 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(20): Show |
25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141-520C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351290 | |||||||
| chr8:91351313 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1141-497C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351313 | |||||||
| chr8:91351321 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1141-489T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351321 | |||||||
| chr8:91351437 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1141-373A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351437 | |||||||
| chr8:91351468 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(20): Show |
25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141-342G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 9/18 | chr8 | 91351468 | |||||||
| chr8:91351976 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1218+89A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91351976 | |||||||
| chr8:91352227 | C | G | 2 | a0001c0001t0001g0191 a0001c0001t0017g0192 |
2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1218+340C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352227 | |||||||
| chr8:91352523 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-378A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352523 | |||||||
| chr8:91352589 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1219-312C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352589 | |||||||
| chr8:91352888 | G | A | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1219-13G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 10/18 | chr8 | 91352888 | |||||||
| chr8:91353397 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02622.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+401A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353397 | |||||||
| chr8:91353538 | C | T | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1314+542C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353538 | |||||||
| chr8:91353699 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1314+703T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353699 | |||||||
| chr8:91353934 | A | G | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1314+938A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353934 | |||||||
| chr8:91353965 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1314+969T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91353965 | |||||||
| chr8:91354071 | T | TA | 2 | a0001c0001t0001g0013 a0001c0001t0001g0119 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1314+1076dupA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91354071 | ||||||
| chr8:91354282 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+1286T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354282 | |||||||
| chr8:91354397 | G | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(69): Show |
74 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1314+1401G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354397 | |||||||
| chr8:91354635 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1314+1639G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354635 | |||||||
| chr8:91354667 | T | C | 23 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(20): Show |
23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1314+1671T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91354667 | |||||||
| chr8:91355440 | T | C | 23 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(20): Show |
23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1314+2444T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355440 | |||||||
| chr8:91355622 | G | T | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1314+2626G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355622 | |||||||
| chr8:91355809 | G | A | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+2813G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355809 | |||||||
| chr8:91355822 | G | A | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1314+2826G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355822 | |||||||
| chr8:91355836 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0119 others(12): Show |
17 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1314+2840C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355836 | |||||||
| chr8:91355870 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02622.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+2874C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355870 | |||||||
| chr8:91355884 | A | C | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1314+2888A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355884 | |||||||
| chr8:91355891 | G | C | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1314+2895G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355891 | |||||||
| chr8:91355956 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1314+2960C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355956 | |||||||
| chr8:91355971 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1314+2975T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91355971 | |||||||
| chr8:91356063 | CT | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0119 others(12): Show |
17 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1314+3073delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91356063 | ||||||
| chr8:91356178 | G | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1314+3182G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356178 | |||||||
| chr8:91356232 | T | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01123.hp2 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1314+3236T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356232 | |||||||
| chr8:91356364 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(78): Show |
83 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.1314+3368G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356364 | |||||||
| chr8:91356432 | G | A | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+3436G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356432 | |||||||
| chr8:91356434 | G | A | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+3438G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356434 | |||||||
| chr8:91356437 | G | A | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1314+3441G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356437 | |||||||
| chr8:91356473 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0085 a0001c0001t0001g0091 |
3 | HG00733.hp1 HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1314+3477T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356473 | |||||||
| chr8:91356552 | C | G | 7 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0097 others(4): Show |
7 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1314+3556C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356552 | |||||||
| chr8:91356792 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1314+3796A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356792 | |||||||
| chr8:91356839 | A | G | 3 | a0001c0001t0005g0108 a0001c0005t0006g0106 a0001c0005t0006g0109 |
3 | HG02970.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1314+3843A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356839 | |||||||
| chr8:91356860 | T | C | 1 | a0003c0006t0011g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1314+3864T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356860 | |||||||
| chr8:91356921 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1314+3925G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91356921 | |||||||
| chr8:91357089 | C | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(9): Show |
14 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1314+4093C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357089 | |||||||
| chr8:91357130 | T | A | 1 | a0001c0002t0002g0148 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1314+4134T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357130 | |||||||
| chr8:91357493 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+4497A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357493 | |||||||
| chr8:91357553 | C | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(20): Show |
25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1314+4557C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357553 | |||||||
| chr8:91357675 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(85): Show |
90 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1315-4678G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357675 | |||||||
| chr8:91357791 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0058 |
2 | NA18989.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1315-4562G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357791 | |||||||
| chr8:91357792 | C | A | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1315-4561C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357792 | |||||||
| chr8:91357951 | A | G | 23 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(20): Show |
23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1315-4402A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357951 | |||||||
| chr8:91357958 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(84): Show |
89 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.1315-4395T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91357958 | |||||||
| chr8:91358032 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315-4321G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358032 | |||||||
| chr8:91358039 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(84): Show |
89 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.1315-4314A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358039 | |||||||
| chr8:91358086 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315-4267C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358086 | |||||||
| chr8:91358087 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1315-4266G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358087 | |||||||
| chr8:91358329 | C | CT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(32): Show |
37 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1315-4007dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91358329 | ||||||
| chr8:91358329 | CT | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0168 a0001c0002t0001g0103 others(5): Show |
8 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315-4007delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91358329 | ||||||
| chr8:91358415 | A | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0071 |
2 | HG02015.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1315-3938A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358415 | |||||||
| chr8:91358553 | A | G | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-3800A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358553 | |||||||
| chr8:91358595 | G | T | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1315-3758G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358595 | |||||||
| chr8:91358636 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(79): Show |
84 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1315-3717A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358636 | |||||||
| chr8:91358649 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1315-3704G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358649 | |||||||
| chr8:91358811 | C | T | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315-3542C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358811 | |||||||
| chr8:91358924 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1315-3429C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358924 | |||||||
| chr8:91358985 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1315-3368C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91358985 | |||||||
| chr8:91359606 | A | T | 3 | a0001c0001t0001g0030 a0003c0009t0011g0138 a0004c0011t0014g0022 |
3 | HG01243.hp2 HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1315-2747A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359606 | |||||||
| chr8:91359727 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1315-2626G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359727 | |||||||
| chr8:91359780 | T | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1315-2573T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359780 | |||||||
| chr8:91359876 | A | ATG | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1315-2458_1315-245 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | ||||||
| chr8:91359876 | A | ATGTGTG | 7 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315-2462_1315-245 others(10): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | ||||||
| chr8:91359876 | A | ATGTGTGT others(1): Show |
1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1315-2464_1315-245 others(12): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | ||||||
| chr8:91359876 | A | ATGTGTGT others(3): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0200 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1315-2466_1315-245 others(14): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | ||||||
| chr8:91359876 | A | G | 1 | a0001c0007t0002g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1315-2477A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359876 | |||||||
| chr8:91359876 | ATG | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(6): Show |
9 | HG01261.hp2 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315-2458_1315-245 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359876 | ||||||
| chr8:91359895 | T | TGC | 45 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(42): Show |
45 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1315-2455_1315-245 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359895 | ||||||
| chr8:91359895 | T | TGTGC | 2 | a0001c0002t0015g0024 a0001c0002t0022g0023 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1315-2457_1315-245 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91359895 | ||||||
| chr8:91359897 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0025 others(21): Show |
26 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1315-2456C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91359897 | |||||||
| chr8:91360257 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1315-2096A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91360257 | |||||||
| chr8:91360306 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1315-2047T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91360306 | |||||||
| chr8:91360487 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1315-1866T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91360487 | |||||||
| chr8:91361567 | A | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1315-786A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91361567 | |||||||
| chr8:91361815 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(84): Show |
89 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.1315-538C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91361815 | |||||||
| chr8:91362080 | T | G | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1315-273T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | chr8 | 91362080 | |||||||
| chr8:91362132 | TAAA | T | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-219_1315-217d others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 91362132 | ||||||
| chr8:91362515 | T | C | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1421+56T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91362515 | |||||||
| chr8:91362525 | A | G | 23 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(20): Show |
23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1421+66A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91362525 | |||||||
| chr8:91362653 | G | T | 10 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(7): Show |
10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421+194G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91362653 | |||||||
| chr8:91363413 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1422-59A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 12/18 | chr8 | 91363413 | |||||||
| chr8:91363941 | GT | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(83): Show |
88 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.1488+420delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 91363941 | ||||||
| chr8:91363961 | T | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1488+423T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91363961 | |||||||
| chr8:91364143 | C | T | 2 | a0001c0002t0015g0024 a0001c0002t0022g0023 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1488+605C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364143 | |||||||
| chr8:91364169 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1488+631G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364169 | |||||||
| chr8:91364495 | C | T | 1 | a0001c0001t0007g0005 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1488+957C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364495 | |||||||
| chr8:91364958 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0127 a0001c0001t0005g0108 others(2): Show |
5 | HG01261.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488+1420G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91364958 | |||||||
| chr8:91365047 | C | CTCT | 82 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(79): Show |
84 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1488+1512_1488+151 others(7): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 91365047 | ||||||
| chr8:91365133 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1489-1447C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365133 | |||||||
| chr8:91365163 | AT | A | 23 | a0001c0002t0001g0027 a0001c0002t0001g0053 a0001c0002t0001g0054 others(20): Show |
23 | HG00733.hp2 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1489-1409delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr8 | 91365163 | ||||||
| chr8:91365528 | G | C | 39 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0032 others(36): Show |
39 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1489-1052G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365528 | |||||||
| chr8:91365582 | G | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1489-998G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365582 | |||||||
| chr8:91365753 | T | C | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1489-827T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91365753 | |||||||
| chr8:91366188 | T | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1489-392T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366188 | |||||||
| chr8:91366255 | A | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(20): Show |
25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1489-325A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366255 | |||||||
| chr8:91366354 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1489-226T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366354 | |||||||
| chr8:91366419 | C | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0097 others(4): Show |
7 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1489-161C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366419 | |||||||
| chr8:91366554 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(20): Show |
25 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1489-26C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 13/18 | chr8 | 91366554 | |||||||
| chr8:91366930 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1626+213G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91366930 | |||||||
| chr8:91367099 | C | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1626+382C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367099 | |||||||
| chr8:91367168 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1626+451C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367168 | |||||||
| chr8:91367259 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1626+542C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367259 | |||||||
| chr8:91367299 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1626+582C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367299 | |||||||
| chr8:91367387 | C | T | 10 | a0001c0002t0002g0046 a0001c0002t0002g0047 a0001c0002t0002g0070 others(7): Show |
10 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+670C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367387 | |||||||
| chr8:91367488 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1626+771G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367488 | |||||||
| chr8:91367577 | A | AG | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(70): Show |
75 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.1626+860_1626+861i others(3): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367577 | |||||||
| chr8:91367639 | T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1626+922T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367639 | |||||||
| chr8:91367851 | A | G | 10 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(7): Show |
10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+1134A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367851 | |||||||
| chr8:91367854 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1626+1137G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367854 | |||||||
| chr8:91367943 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1626+1226C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91367943 | |||||||
| chr8:91368033 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1626+1316C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368033 | |||||||
| chr8:91368164 | A | G | 1 | a0001c0002t0012g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1626+1447A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368164 | |||||||
| chr8:91368413 | G | GT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(11): Show |
14 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627-1361dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 91368413 | ||||||
| chr8:91368413 | G | GTT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(69): Show |
74 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1627-1362_1627-136 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 91368413 | ||||||
| chr8:91368425 | G | T | 1 | a0001c0001t0005g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1627-1360G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368425 | |||||||
| chr8:91368431 | T | G | 10 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(7): Show |
10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-1354T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368431 | |||||||
| chr8:91368581 | G | A | 1 | a0003c0009t0011g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1627-1204G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368581 | |||||||
| chr8:91368667 | C | T | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627-1118C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368667 | |||||||
| chr8:91368944 | C | A | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1627-841C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368944 | |||||||
| chr8:91368981 | C | T | 2 | a0002c0003t0001g0135 a0002c0003t0001g0136 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1627-804C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368981 | |||||||
| chr8:91368984 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1627-801T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91368984 | |||||||
| chr8:91369143 | C | T | 10 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(7): Show |
10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-642C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91369143 | |||||||
| chr8:91369369 | GT | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
190 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1627-403delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr8 | 91369369 | ||||||
| chr8:91369385 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1627-400T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91369385 | |||||||
| chr8:91369428 | T | C | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1627-357T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 14/18 | chr8 | 91369428 | |||||||
| chr8:91370079 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1675+246C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370079 | |||||||
| chr8:91370121 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1675+288C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370121 | |||||||
| chr8:91370139 | A | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(14): Show |
18 | HG00642.hp1 HG00738.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1675+306A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370139 | |||||||
| chr8:91370141 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1675+308T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370141 | |||||||
| chr8:91370178 | C | CT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(71): Show |
76 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1675+354dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91370178 | ||||||
| chr8:91370197 | C | CCTT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(85): Show |
91 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1675+366_1675+367i others(5): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91370197 | ||||||
| chr8:91370579 | C | T | 54 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(51): Show |
54 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1675+746C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370579 | |||||||
| chr8:91370798 | G | C | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675+965G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91370798 | |||||||
| chr8:91371268 | T | A | 5 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675+1435T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371268 | |||||||
| chr8:91371550 | TG | T | 24 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(21): Show |
24 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1675+1718delG | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371550 | |||||||
| chr8:91371566 | A | T | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1675+1733A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371566 | |||||||
| chr8:91371702 | T | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(187): Show |
193 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.1675+1869T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371702 | |||||||
| chr8:91371731 | T | C | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675+1898T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371731 | |||||||
| chr8:91371849 | C | T | 2 | a0001c0002t0015g0024 a0001c0002t0022g0023 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1675+2016C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371849 | |||||||
| chr8:91371901 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1675+2068G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91371901 | |||||||
| chr8:91372225 | G | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1675+2392G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372225 | |||||||
| chr8:91372279 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1675+2446T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372279 | |||||||
| chr8:91372356 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0028 others(44): Show |
48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1675+2523A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372356 | |||||||
| chr8:91372365 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01123.hp2 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1675+2532C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372365 | |||||||
| chr8:91372396 | A | C | 13 | a0001c0002t0001g0045 a0001c0002t0001g0110 a0001c0002t0001g0112 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+2563A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372396 | |||||||
| chr8:91372560 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1675+2727T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372560 | |||||||
| chr8:91372650 | G | A | 5 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(2): Show |
5 | HG00642.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675+2817G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91372650 | |||||||
| chr8:91372972 | AT | A | 3 | a0001c0002t0002g0070 a0001c0004t0002g0144 a0001c0004t0002g0159 |
3 | NA18947.hp2 NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1675+3146delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91372972 | ||||||
| chr8:91373120 | T | G | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675+3287T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373120 | |||||||
| chr8:91373287 | T | A | 1 | a0001c0002t0003g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1675+3454T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373287 | |||||||
| chr8:91373371 | G | C | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1675+3538G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373371 | |||||||
| chr8:91373428 | G | A | 5 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675+3595G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373428 | |||||||
| chr8:91373801 | A | G | 10 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(7): Show |
10 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1675+3968A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91373801 | |||||||
| chr8:91374385 | G | GT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0160 others(3): Show |
6 | HG02055.hp1 NA18989.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+4563dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91374385 | ||||||
| chr8:91374385 | GT | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0040 others(50): Show |
53 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1675+4563delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91374385 | ||||||
| chr8:91374639 | T | G | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1675+4806T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91374639 | |||||||
| chr8:91374804 | A | T | 1 | a0001c0002t0003g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1675+4971A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91374804 | |||||||
| chr8:91375151 | T | C | 2 | a0001c0001t0007g0005 a0001c0001t0007g0006 |
2 | NA19006.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1675+5318T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375151 | |||||||
| chr8:91375261 | G | GT | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(10): Show |
13 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1675+5432dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91375261 | ||||||
| chr8:91375269 | T | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(51): Show |
54 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1675+5436T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375269 | |||||||
| chr8:91375487 | T | A | 1 | a0001c0002t0006g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1675+5654T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375487 | |||||||
| chr8:91375636 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1675+5803C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375636 | |||||||
| chr8:91375660 | GT | G | 41 | a0001c0001t0001g0030 a0001c0002t0001g0014 a0001c0002t0001g0015 others(38): Show |
41 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1675+5841delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91375660 | ||||||
| chr8:91375857 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1675+6024C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375857 | |||||||
| chr8:91375907 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1675+6074A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91375907 | |||||||
| chr8:91376078 | G | T | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1675+6245G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91376078 | |||||||
| chr8:91376763 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1675+6930C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91376763 | |||||||
| chr8:91376857 | A | G | 3 | a0001c0001t0005g0108 a0001c0005t0006g0106 a0001c0005t0006g0109 |
3 | HG02970.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1675+7024A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91376857 | |||||||
| chr8:91377099 | G | T | 3 | a0001c0001t0010g0092 a0001c0001t0010g0093 a0001c0001t0010g0094 |
3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1675+7266G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377099 | |||||||
| chr8:91377197 | A | T | 1 | a0001c0001t0001g0003 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1675+7364A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377197 | |||||||
| chr8:91377230 | G | T | 1 | a0001c0002t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1675+7397G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377230 | |||||||
| chr8:91377284 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1675+7451C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377284 | |||||||
| chr8:91377323 | C | A | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1675+7490C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377323 | |||||||
| chr8:91377498 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1675+7665G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377498 | |||||||
| chr8:91377655 | C | G | 41 | a0001c0001t0001g0030 a0001c0002t0001g0014 a0001c0002t0001g0015 others(38): Show |
41 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1675+7822C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377655 | |||||||
| chr8:91377714 | G | T | 1 | a0001c0002t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1675+7881G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377714 | |||||||
| chr8:91377789 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1675+7956C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377789 | |||||||
| chr8:91377790 | G | C | 1 | a0001c0001t0001g0033 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1675+7957G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91377790 | |||||||
| chr8:91378298 | A | C | 4 | a0001c0001t0001g0200 a0001c0001t0009g0201 a0001c0001t0009g0207 others(1): Show |
4 | HG02572.hp2 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+8465A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378298 | |||||||
| chr8:91378499 | AG | A | 14 | a0001c0002t0001g0027 a0001c0002t0001g0080 a0001c0002t0001g0186 others(11): Show |
14 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1675+8668delG | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91378499 | ||||||
| chr8:91378561 | A | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1675+8728A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378561 | |||||||
| chr8:91378779 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0028 others(44): Show |
48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1675+8946C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378779 | |||||||
| chr8:91378887 | C | T | 1 | a0001c0001t0005g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1675+9054C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91378887 | |||||||
| chr8:91379061 | TA | T | 13 | a0001c0002t0001g0027 a0001c0002t0001g0080 a0001c0002t0001g0186 others(10): Show |
13 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+9236delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91379061 | ||||||
| chr8:91379224 | A | G | 2 | a0001c0001t0004g0202 a0001c0001t0018g0124 |
2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1675+9391A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379224 | |||||||
| chr8:91379302 | G | A | 1 | a0001c0002t0015g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1675+9469G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379302 | |||||||
| chr8:91379553 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1675+9720A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379553 | |||||||
| chr8:91379642 | A | G | 40 | a0001c0001t0001g0030 a0001c0002t0001g0014 a0001c0002t0001g0015 others(37): Show |
40 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-9696A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379642 | |||||||
| chr8:91379723 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-9615A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379723 | |||||||
| chr8:91379883 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1676-9455A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379883 | |||||||
| chr8:91379938 | A | G | 3 | a0001c0002t0001g0045 a0001c0002t0001g0110 a0001c0002t0001g0112 |
3 | HG02280.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1676-9400A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379938 | |||||||
| chr8:91379957 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(187): Show |
193 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.1676-9381G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91379957 | |||||||
| chr8:91380034 | T | C | 13 | a0001c0002t0001g0045 a0001c0002t0001g0110 a0001c0002t0001g0112 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1676-9304T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380034 | |||||||
| chr8:91380198 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1676-9140G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380198 | |||||||
| chr8:91380525 | T | G | 4 | a0001c0001t0001g0043 a0001c0001t0002g0007 a0001c0001t0002g0063 others(1): Show |
4 | HG02148.hp1 HG02300.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-8813T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380525 | |||||||
| chr8:91380666 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1676-8672A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91380666 | |||||||
| chr8:91381020 | GA | G | 3 | a0001c0002t0001g0045 a0001c0002t0001g0110 a0001c0002t0001g0112 |
3 | HG02280.hp2 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1676-8312delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91381020 | ||||||
| chr8:91381330 | C | A | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1676-8008C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381330 | |||||||
| chr8:91381619 | A | G | 13 | a0001c0002t0001g0045 a0001c0002t0001g0110 a0001c0002t0001g0112 others(10): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1676-7719A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381619 | |||||||
| chr8:91381773 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02015.hp2 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1676-7565C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381773 | |||||||
| chr8:91381969 | C | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1676-7369C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381969 | |||||||
| chr8:91381980 | G | C | 40 | a0001c0001t0001g0030 a0001c0002t0001g0014 a0001c0002t0001g0015 others(37): Show |
40 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-7358G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91381980 | |||||||
| chr8:91382068 | T | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(50): Show |
53 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1676-7270T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382068 | |||||||
| chr8:91382385 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1676-6953C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382385 | |||||||
| chr8:91382851 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1676-6487G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382851 | |||||||
| chr8:91382918 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0119 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1676-6420T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382918 | |||||||
| chr8:91382931 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1676-6407C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91382931 | |||||||
| chr8:91383115 | A | G | 1 | a0001c0002t0008g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1676-6223A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383115 | |||||||
| chr8:91383135 | C | T | 3 | a0001c0002t0001g0103 a0001c0002t0009g0102 a0001c0002t0012g0100 |
3 | HG00735.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1676-6203C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383135 | |||||||
| chr8:91383142 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1676-6196C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383142 | |||||||
| chr8:91383233 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0021g0206 |
3 | HG02145.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1676-6105A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383233 | |||||||
| chr8:91383272 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(10): Show |
13 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1676-6066T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383272 | |||||||
| chr8:91383366 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(10): Show |
13 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1676-5972G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383366 | |||||||
| chr8:91383544 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(10): Show |
13 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1676-5794G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383544 | |||||||
| chr8:91383627 | C | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(10): Show |
13 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1676-5711C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383627 | |||||||
| chr8:91383862 | T | C | 14 | a0001c0002t0001g0027 a0001c0002t0001g0080 a0001c0002t0001g0186 others(11): Show |
14 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-5476T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91383862 | |||||||
| chr8:91384035 | G | A | 1 | a0001c0002t0003g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1676-5303G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384035 | |||||||
| chr8:91384051 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(62): Show |
67 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1676-5287G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384051 | |||||||
| chr8:91384193 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1676-5145G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384193 | |||||||
| chr8:91384298 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-5040G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384298 | |||||||
| chr8:91384704 | G | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(47): Show |
50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1676-4634G>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384704 | |||||||
| chr8:91384719 | T | C | 2 | a0001c0001t0001g0030 a0004c0011t0014g0022 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1676-4619T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384719 | |||||||
| chr8:91384764 | G | GAGGA | 6 | a0001c0001t0001g0164 a0001c0001t0001g0177 a0001c0002t0001g0053 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1676-4544_1676-454 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91384764 | ||||||
| chr8:91384764 | GAGGA | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(38): Show |
43 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1676-4544_1676-454 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91384764 | ||||||
| chr8:91384769 | AGGAAGGA others(2): Show |
A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-4567_1676-455 others(13): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91384769 | ||||||
| chr8:91384896 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-4442A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384896 | |||||||
| chr8:91384906 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-4432T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384906 | |||||||
| chr8:91384914 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0025 others(112): Show |
116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1676-4424T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91384914 | |||||||
| chr8:91385125 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1676-4213T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385125 | |||||||
| chr8:91385165 | C | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-4173C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385165 | |||||||
| chr8:91385188 | A | G | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1676-4150A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385188 | |||||||
| chr8:91385248 | T | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-4090T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385248 | |||||||
| chr8:91385486 | C | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(47): Show |
50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1676-3852C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385486 | |||||||
| chr8:91385513 | C | T | 6 | a0001c0002t0001g0027 a0001c0002t0001g0080 a0001c0002t0001g0186 others(3): Show |
6 | HG00733.hp2 HG00741.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1676-3825C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385513 | |||||||
| chr8:91385628 | T | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-3710T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91385628 | |||||||
| chr8:91386062 | A | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(47): Show |
50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1676-3276A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386062 | |||||||
| chr8:91386134 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-3204T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386134 | |||||||
| chr8:91386482 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-2856A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386482 | |||||||
| chr8:91386604 | C | A | 40 | a0001c0001t0001g0030 a0001c0002t0001g0014 a0001c0002t0001g0015 others(37): Show |
40 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-2734C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386604 | |||||||
| chr8:91386646 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-2692C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91386646 | |||||||
| chr8:91387177 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-2161A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387177 | |||||||
| chr8:91387244 | T | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-2094T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387244 | |||||||
| chr8:91387445 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1676-1893C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387445 | |||||||
| chr8:91387628 | GAATC | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(59): Show |
64 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1676-1705_1676-170 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91387628 | ||||||
| chr8:91387696 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0127 |
2 | HG01261.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1676-1642T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387696 | |||||||
| chr8:91387717 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-1621A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387717 | |||||||
| chr8:91387789 | T | C | 1 | a0005c0010t0001g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1676-1549T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91387789 | |||||||
| chr8:91388091 | T | C | 2 | a0001c0005t0006g0106 a0001c0005t0006g0109 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1676-1247T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388091 | |||||||
| chr8:91388118 | A | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1220A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388118 | |||||||
| chr8:91388153 | C | A | 2 | a0002c0003t0001g0135 a0002c0003t0001g0136 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1676-1185C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388153 | |||||||
| chr8:91388176 | A | G | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1162A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388176 | |||||||
| chr8:91388217 | A | G | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1121A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388217 | |||||||
| chr8:91388235 | G | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-1103G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388235 | |||||||
| chr8:91388238 | C | CTCCTGCC others(109): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0021g0206 |
3 | HG02145.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1676-1066_1676-951 others(119): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | 91388238 | ||||||
| chr8:91388353 | C | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-985C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388353 | |||||||
| chr8:91388417 | C | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-921C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388417 | |||||||
| chr8:91388429 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(9): Show |
14 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-909A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388429 | |||||||
| chr8:91388461 | T | C | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-877T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388461 | |||||||
| chr8:91388576 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1676-762A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388576 | |||||||
| chr8:91388863 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1676-475T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388863 | |||||||
| chr8:91388875 | A | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-463A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388875 | |||||||
| chr8:91388892 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02622.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1676-446A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91388892 | |||||||
| chr8:91389229 | A | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0001g0141 others(9): Show |
14 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-109A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91389229 | |||||||
| chr8:91389293 | G | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-45G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91389293 | |||||||
| chr8:91389304 | C | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1676-34C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 15/18 | chr8 | 91389304 | |||||||
| chr8:91389642 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1776+204G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389642 | |||||||
| chr8:91389710 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1776+272G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389710 | |||||||
| chr8:91389722 | G | T | 7 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0004g0095 others(4): Show |
7 | HG00642.hp1 HG02055.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1776+284G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389722 | |||||||
| chr8:91389858 | T | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(185): Show |
191 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.1776+420T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389858 | |||||||
| chr8:91389979 | A | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0039 others(60): Show |
63 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1776+541A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91389979 | |||||||
| chr8:91390034 | A | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+596A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390034 | |||||||
| chr8:91390090 | T | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+652T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390090 | |||||||
| chr8:91390103 | CA | C | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+666delA | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390103 | |||||||
| chr8:91390110 | C | CT | 19 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0122 others(16): Show |
19 | HG00735.hp1 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1776+688dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390110 | ||||||
| chr8:91390110 | C | CTT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0143 a0001c0001t0002g0001 others(2): Show |
7 | HG01891.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1776+687_1776+688d others(4): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390110 | ||||||
| chr8:91390110 | CT | C | 16 | a0001c0001t0001g0010 a0001c0002t0001g0045 a0001c0002t0001g0054 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1776+688delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390110 | ||||||
| chr8:91390209 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(36): Show |
41 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1776+771T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390209 | |||||||
| chr8:91390308 | G | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+870G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390308 | |||||||
| chr8:91390359 | T | C | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+921T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390359 | |||||||
| chr8:91390482 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1776+1044C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390482 | |||||||
| chr8:91390541 | C | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1103C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390541 | |||||||
| chr8:91390664 | A | ATACT | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1228_1776+122 others(8): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390664 | ||||||
| chr8:91390675 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1776+1237C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390675 | |||||||
| chr8:91390679 | T | C | 6 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1776+1241T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390679 | |||||||
| chr8:91390711 | A | ATC | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1278_1776+127 others(6): Show |
SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91390711 | ||||||
| chr8:91390768 | A | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1330A>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390768 | |||||||
| chr8:91390788 | C | T | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1776+1350C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390788 | |||||||
| chr8:91390794 | C | T | 1 | a0001c0002t0015g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1776+1356C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390794 | |||||||
| chr8:91390912 | T | C | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1474T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390912 | |||||||
| chr8:91390920 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0101 others(7): Show |
10 | HG00642.hp1 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1776+1482G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91390920 | |||||||
| chr8:91391062 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1776+1624G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391062 | |||||||
| chr8:91391216 | T | G | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1778T>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391216 | |||||||
| chr8:91391286 | G | T | 4 | a0001c0001t0001g0200 a0001c0001t0009g0201 a0001c0001t0009g0207 others(1): Show |
4 | HG02896.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1776+1848G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391286 | |||||||
| chr8:91391333 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0021g0206 |
3 | HG02145.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1776+1895T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391333 | |||||||
| chr8:91391363 | G | T | 2 | a0002c0003t0001g0135 a0002c0003t0001g0136 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1776+1925G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391363 | |||||||
| chr8:91391394 | C | T | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1776+1956C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391394 | |||||||
| chr8:91391609 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02015.hp2 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1776+2171C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391609 | |||||||
| chr8:91391651 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1777-2146C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391651 | |||||||
| chr8:91391682 | A | G | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-2115A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391682 | |||||||
| chr8:91391751 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0184 |
2 | HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1777-2046A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391751 | |||||||
| chr8:91391802 | A | AT | 9 | a0001c0002t0001g0045 a0001c0002t0002g0046 a0001c0002t0002g0047 others(6): Show |
9 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1777-1982dupT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 91391802 | ||||||
| chr8:91391872 | A | G | 2 | a0001c0002t0002g0046 a0001c0002t0002g0047 |
2 | HG01070.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1777-1925A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391872 | |||||||
| chr8:91391975 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0030 others(9): Show |
12 | HG00642.hp1 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1777-1822G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391975 | |||||||
| chr8:91391982 | T | C | 14 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1777-1815T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91391982 | |||||||
| chr8:91392098 | C | T | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1777-1699C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392098 | |||||||
| chr8:91392426 | G | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-1371G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392426 | |||||||
| chr8:91392530 | T | C | 1 | a0001c0002t0005g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1777-1267T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392530 | |||||||
| chr8:91392624 | C | G | 14 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
15 | HG01123.hp2 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1777-1173C>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392624 | |||||||
| chr8:91392656 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1777-1141G>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91392656 | |||||||
| chr8:91393092 | C | A | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-705C>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393092 | |||||||
| chr8:91393108 | A | G | 1 | a0001c0001t0013g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1777-689A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393108 | |||||||
| chr8:91393453 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1777-344T>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393453 | |||||||
| chr8:91393497 | A | C | 2 | a0003c0006t0011g0069 a0003c0009t0011g0138 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1777-300A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393497 | |||||||
| chr8:91393560 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1777-237G>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393560 | |||||||
| chr8:91393711 | A | G | 1 | a0001c0002t0008g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1777-86A>G | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393711 | |||||||
| chr8:91393793 | C | T | 11 | a0001c0002t0001g0045 a0001c0002t0002g0046 a0001c0002t0002g0047 others(8): Show |
11 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1777-4C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 16/18 | chr8 | 91393793 | |||||||
| chr8:91393874 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1831+23C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 17/18 | chr8 | 91393874 | |||||||
| chr8:91394141 | A | C | 1 | a0004c0011t0014g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1935+102A>C | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | chr8 | 91394141 | |||||||
| chr8:91394208 | CT | C | 18 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0007 others(15): Show |
19 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1935+176delT | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr8 | 91394208 | ||||||
| chr8:91394606 | C | T | 2 | a0001c0001t0001g0060 a0001c0002t0001g0045 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1936-456C>T | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | chr8 | 91394606 | |||||||
| chr8:91394931 | T | A | 6 | a0001c0001t0004g0188 a0001c0001t0004g0202 a0001c0002t0004g0203 others(3): Show |
6 | HG00642.hp1 HG00738.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-131T>A | SLC26A7 | ENSG00000147606.9 | transcript | ENST00000276609.8 | protein_coding | 18/18 | chr8 | 91394931 |