Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6337 |
| ensemblid | ENSG00000111319.13 |
| hgncid | 10599 |
| symbol | SCNN1A |
| name | sodium channel epithelial 1 subunit alpha |
| refseq_nuc | NM_001038.6 |
| refseq_prot | NP_001029.1 |
| ensembl_nuc | ENST00000228916.7 |
| ensembl_prot | ENSP00000228916.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 6346847 |
| end | 6375563 |
| strand | - |
| ver | v1.2 |
| region | chr12:6346847-6375563 |
| region5000 | chr12:6341847-6380563 |
| regionname0 | SCNN1A_chr12_6346847_6375563 |
| regionname5000 | SCNN1A_chr12_6341847_6380563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 669 | 239 | 50 | 59 | 89 | 10 | 30 | 75 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0002 | 1/0 | 669 | 102 | 4 | 13 | 72 | 3 | 9 | 43 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0003 | 0/0 | 669 | 65 | 31 | 5 | 25 | 0 | 4 | 19 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0004 | 0/0 | 669 | 13 | 2 | 0 | 11 | 0 | 0 | 11 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0005 | 0/0 | 669 | 10 | 0 | 3 | 7 | 0 | 0 | 6 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0006 | 0/0 | 669 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0007 | 0/0 | 669 | 5 | 0 | 3 | 0 | 1 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0008 | 0/0 | 669 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0009 | 0/0 | 669 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0010 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0011 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0012 | 0/0 | 669 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0013 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0014 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0015 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0016 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0017 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| a0018 | 0/0 | 669 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | MEGNK others(664): Show |
chr12 | 6341847 | 6380563 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2007 | 221 | 40 | 59 | 83 | 10 | 28 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0001c0004 | 0/0 | 2007 | 10 | 10 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0001c0006 | 0/0 | 2007 | 7 | 0 | 0 | 5 | 0 | 2 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0001c0029 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0002c0002 | 1/0 | 2007 | 96 | 4 | 13 | 67 | 3 | 8 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0002c0011 | 0/0 | 2007 | 5 | 0 | 0 | 4 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0002c0028 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0003c0003 | 0/0 | 2007 | 59 | 31 | 5 | 19 | 0 | 4 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0003c0010 | 0/0 | 2007 | 5 | 0 | 0 | 5 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0003c0018 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0004c0009 | 0/0 | 2007 | 5 | 2 | 0 | 3 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0004c0012 | 0/0 | 2007 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0004c0014 | 0/0 | 2007 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0005c0007 | 0/0 | 2007 | 6 | 0 | 3 | 3 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0005c0013 | 0/0 | 2007 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0006c0005 | 0/0 | 2007 | 7 | 7 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0006c0026 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0007c0008 | 0/0 | 2007 | 5 | 0 | 3 | 0 | 1 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0008c0015 | 0/0 | 2007 | 2 | 0 | 1 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0009c0016 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0010c0017 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0011c0022 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0012c0021 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0013c0023 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0014c0020 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0015c0027 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0016c0025 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0017c0019 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 | ||
| a0018c0024 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | ATGGA others(2002): Show |
chr12 | 6341847 | 6380563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3149 | 157 | 30 | 34 | 70 | 3 | 20 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0002 | 0/1 | 3149 | 52 | 2 | 25 | 11 | 6 | 7 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0003 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0004 | 0/0 | 3149 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0005 | 0/0 | 3149 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0009 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0011 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0013 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0014 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0015 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0001t0016 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0004t0001 | 0/0 | 3149 | 9 | 9 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0004t0004 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0006t0001 | 0/0 | 3149 | 6 | 0 | 0 | 5 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0006t0019 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0001c0029t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0001 | 0/0 | 3149 | 71 | 1 | 8 | 54 | 1 | 7 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0002 | 1/0 | 3149 | 18 | 2 | 4 | 9 | 1 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0004 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0007 | 0/0 | 3149 | 3 | 0 | 0 | 3 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0010 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0012 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0002t0018 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0011t0001 | 0/0 | 3149 | 5 | 0 | 0 | 4 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0002c0028t0003 | 0/0 | 3145 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0003c0003t0001 | 0/0 | 3149 | 49 | 25 | 4 | 18 | 0 | 2 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0003c0003t0002 | 0/0 | 3149 | 5 | 2 | 0 | 1 | 0 | 2 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0003c0003t0004 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0003c0003t0005 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0003c0003t0006 | 0/0 | 3145 | 3 | 2 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0003c0010t0001 | 0/0 | 3149 | 5 | 0 | 0 | 5 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0003c0018t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0004c0009t0003 | 0/0 | 3145 | 4 | 1 | 0 | 3 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0004c0009t0008 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0004c0012t0003 | 0/0 | 3145 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0004c0014t0003 | 0/0 | 3145 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0005c0007t0001 | 0/0 | 3149 | 5 | 0 | 3 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0005c0007t0002 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0005c0013t0001 | 0/0 | 3149 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0006c0005t0003 | 0/0 | 3145 | 6 | 6 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0006c0005t0008 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0006c0026t0003 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0007c0008t0001 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0007c0008t0002 | 0/0 | 3149 | 4 | 0 | 2 | 0 | 1 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0008c0015t0001 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0008c0015t0017 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0009c0016t0001 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0010c0017t0001 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0011c0022t0001 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0012c0021t0001 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0013c0023t0003 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3140): Show |
chr12 | 6341847 | 6380563 |
| a0014c0020t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0015c0027t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0016c0025t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0017c0019t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| a0018c0024t0001 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | GCTTC others(3144): Show |
chr12 | 6341847 | 6380563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0392 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0398 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0001g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0004g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0004g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0013g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0014g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0015g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0001t0016g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0001g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0004t0004g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0006t0019g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0001c0029t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0001g0400 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0004g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0012g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0002t0018g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0011t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0011t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0011t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0011t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0011t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0002c0028t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0001g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0004g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0003t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0010t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0010t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0010t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0010t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0003c0018t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0009t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0009t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0009t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0009t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0009t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0012t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0012t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0012t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0012t0003g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0014t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0014t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0014t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0004c0014t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0007t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0007t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0007t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0007t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0007t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0007t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0013t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0013t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0005c0013t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0005t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0006c0026t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0007c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0007c0008t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0007c0008t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0007c0008t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0008c0015t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0008c0015t0017g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0009c0016t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0010c0017t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0011c0022t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0012c0021t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0013c0023t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0014c0020t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0015c0027t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0016c0025t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0017c0019t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| a0018c0024t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00099 | hp2 | a0002 | c0002 | t0012 | g0057 | EUR | GBR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | GBR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | FIN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00280 | hp2 | a0009 | c0016 | t0001 | g0140 | EUR | FIN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0392 | EUR | FIN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00323 | hp2 | a0001 | c0001 | t0016 | g0176 | EUR | FIN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00438 | hp2 | a0002 | c0011 | t0001 | g0129 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0217 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0379 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0397 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0402 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01074 | hp2 | a0008 | c0015 | t0017 | g0368 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0284 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01167 | hp2 | a0005 | c0007 | t0001 | g0200 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01169 | hp1 | a0005 | c0007 | t0001 | g0201 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01175 | hp2 | a0007 | c0008 | t0001 | g0171 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01192 | hp2 | a0003 | c0003 | t0006 | g0230 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0396 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0394 | AMR | PUR | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01256 | hp1 | a0007 | c0008 | t0002 | g0008 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01258 | hp1 | a0007 | c0008 | t0002 | g0080 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01261 | hp1 | a0005 | c0007 | t0001 | g0228 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0103 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0242 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01515 | hp1 | a0007 | c0008 | t0002 | g0008 | EUR | IBS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0162 | EUR | IBS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01884 | hp1 | a0003 | c0003 | t0006 | g0231 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01884 | hp2 | a0006 | c0005 | t0003 | g0143 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0371 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0244 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0389 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01981 | hp2 | a0002 | c0002 | t0018 | g0370 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0168 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0406 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0385 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02132 | hp1 | a0005 | c0013 | t0001 | g0010 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02132 | hp2 | a0003 | c0010 | t0001 | g0011 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02145 | hp2 | a0006 | c0005 | t0003 | g0353 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02155 | hp1 | a0002 | c0002 | t0007 | g0250 | EAS | CDX | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CDX | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | CDX | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | CDX | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0212 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02258 | hp1 | a0003 | c0003 | t0002 | g0087 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0275 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0233 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0102 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02572 | hp2 | a0010 | c0017 | t0001 | g0344 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0374 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0041 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02622 | hp1 | a0006 | c0005 | t0003 | g0136 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02630 | hp2 | a0004 | c0009 | t0008 | g0321 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02647 | hp1 | a0006 | c0005 | t0008 | g0243 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0101 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0407 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0227 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0398 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02818 | hp1 | a0002 | c0002 | t0004 | g0403 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0207 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0208 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0409 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0323 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0234 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0380 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0328 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0165 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03130 | hp1 | a0004 | c0009 | t0003 | g0134 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03130 | hp2 | a0006 | c0026 | t0003 | g0109 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0137 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0411 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03209 | hp2 | a0011 | c0022 | t0001 | g0190 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03225 | hp1 | a0001 | c0004 | t0004 | g0404 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0339 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03239 | hp2 | a0012 | c0021 | t0001 | g0169 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03453 | hp1 | a0003 | c0003 | t0005 | g0139 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0408 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0405 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0237 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0410 | AFR | ESN | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0188 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | GWD | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03579 | hp1 | a0013 | c0023 | t0003 | g0359 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0304 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0366 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03669 | hp1 | a0001 | c0006 | t0019 | g0126 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0365 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0383 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0399 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0375 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0369 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03710 | hp2 | a0008 | c0015 | t0001 | g0382 | SAS | PJL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03831 | hp1 | a0002 | c0011 | t0001 | g0122 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0164 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0381 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03927 | hp1 | a0003 | c0003 | t0002 | g0076 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03942 | hp1 | a0001 | c0006 | t0001 | g0113 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0387 | SAS | BEB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0077 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0254 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0390 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0400 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG04228 | hp2 | a0007 | c0008 | t0002 | g0081 | SAS | STU | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18522 | hp2 | a0006 | c0005 | t0003 | g0283 | AFR | YRI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18612 | hp1 | a0003 | c0010 | t0001 | g0118 | EAS | CHB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | CHB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0222 | EAS | CHB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | YRI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0104 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18944 | hp2 | a0001 | c0029 | t0001 | g0112 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18945 | hp1 | a0004 | c0012 | t0003 | g0338 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0362 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18947 | hp2 | a0005 | c0007 | t0001 | g0350 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18950 | hp2 | a0001 | c0006 | t0001 | g0125 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18951 | hp2 | a0001 | c0006 | t0001 | g0121 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18957 | hp2 | a0002 | c0011 | t0001 | g0111 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18963 | hp1 | a0001 | c0006 | t0001 | g0116 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18963 | hp2 | a0002 | c0002 | t0010 | g0095 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18968 | hp2 | a0014 | c0020 | t0001 | g0303 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18969 | hp1 | a0002 | c0002 | t0007 | g0288 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18970 | hp1 | a0005 | c0013 | t0001 | g0010 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18970 | hp2 | a0004 | c0009 | t0003 | g0335 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18971 | hp2 | a0015 | c0027 | t0001 | g0114 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18973 | hp2 | a0004 | c0014 | t0003 | g0110 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18975 | hp2 | a0003 | c0010 | t0001 | g0011 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0388 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18980 | hp2 | a0001 | c0006 | t0001 | g0106 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18981 | hp1 | a0003 | c0010 | t0001 | g0120 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18984 | hp2 | a0005 | c0013 | t0001 | g0130 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18986 | hp1 | a0002 | c0002 | t0007 | g0265 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18987 | hp1 | a0005 | c0013 | t0001 | g0117 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18988 | hp2 | a0002 | c0011 | t0001 | g0124 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18989 | hp2 | a0004 | c0009 | t0003 | g0192 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0115 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0401 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18994 | hp2 | a0004 | c0012 | t0003 | g0333 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0305 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18999 | hp2 | a0002 | c0028 | t0003 | g0127 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19004 | hp1 | a0004 | c0009 | t0003 | g0331 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19004 | hp2 | a0004 | c0014 | t0003 | g0128 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0372 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19011 | hp2 | a0001 | c0001 | t0013 | g0291 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19012 | hp1 | a0005 | c0007 | t0001 | g0186 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0240 | AFR | LWK | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19043 | hp1 | a0006 | c0005 | t0003 | g0156 | AFR | LWK | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19056 | hp1 | a0003 | c0018 | t0001 | g0267 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19056 | hp2 | a0016 | c0025 | t0001 | g0119 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0096 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19060 | hp1 | a0003 | c0010 | t0001 | g0107 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19063 | hp2 | a0004 | c0014 | t0003 | g0108 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19064 | hp1 | a0017 | c0019 | t0001 | g0223 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0302 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0391 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0351 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0395 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19079 | hp1 | a0004 | c0012 | t0003 | g0393 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19079 | hp2 | a0002 | c0011 | t0001 | g0123 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19083 | hp1 | a0003 | c0003 | t0001 | g0386 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0214 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19090 | hp1 | a0004 | c0012 | t0003 | g0336 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19091 | hp2 | a0004 | c0014 | t0003 | g0131 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19240 | hp1 | a0006 | c0005 | t0003 | g0246 | AFR | YRI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0276 | AFR | ASW | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0135 | AFR | ASW | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0072 | EUR | TSI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20752 | hp2 | a0018 | c0024 | t0001 | g0202 | EUR | TSI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | TSI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0281 | SAS | GIH | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | GIH | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | CLM | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0245 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0082 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0282 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0236 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | ACB | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0343 | AFR | MSL | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | USA | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18955 | hp1 | a0005 | c0007 | t0002 | g0073 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20300 | hp1 | a0003 | c0003 | t0006 | g0307 | AFR | USA | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0342 | AFR | LWK | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0274 | AFR | LWK | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0047 | REF | REF | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0040 | REF | REF | SCNN1A_chr12_6341847_6380563 | SCNN1A | chr12 | 6341847 | 6380563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6347896 | T | C | 12 | a0001 a0003 a0004 others(9): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
missense_variant | MODERATE | c.1987A>G | p.Thr663Ala | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 2100/3149 | 1987/2010 | 663/669 | chr12 | 6347896 | |||
| chr12:6348030 | C | A | 3 | a0004 a0006 a0013 |
22 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(19): Show |
missense_variant | MODERATE | c.1853G>T | p.Cys618Phe | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 1966/3149 | 1853/2010 | 618/669 | chr12 | 6348030 | |||
| chr12:6348093 | C | T | 1 | a0016 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.1790G>A | p.Arg597Gln | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 1903/3149 | 1790/2010 | 597/669 | chr12 | 6348093 | |||
| chr12:6348111 | C | T | 1 | a0013 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1772G>A | p.Arg591Gln | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 1885/3149 | 1772/2010 | 591/669 | chr12 | 6348111 | |||
| chr12:6348122 | C | A | 1 | a0015 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1761G>T | p.Arg587Ser | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 1874/3149 | 1761/2010 | 587/669 | chr12 | 6348122 | |||
| chr12:6348166 | C | T | 1 | a0011 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1717G>A | p.Val573Ile | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 1830/3149 | 1717/2010 | 573/669 | chr12 | 6348166 | |||
| chr12:6349177 | G | A | 1 | a0018 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1484C>T | p.Ser495Leu | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/13 | 1597/3149 | 1484/2010 | 495/669 | chr12 | 6349177 | |||
| chr12:6349184 | A | G | 3 | a0007 a0009 a0012 |
7 | HG00280.hp2 HG01175.hp2 HG01256.hp1 others(4): Show |
missense_variant | MODERATE | c.1477T>C | p.Trp493Arg | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/13 | 1590/3149 | 1477/2010 | 493/669 | chr12 | 6349184 | |||
| chr12:6354787 | G | T | 1 | a0014 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1205C>A | p.Pro402His | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 7/13 | 1318/3149 | 1205/2010 | 402/669 | chr12 | 6354787 | |||
| chr12:6355352 | C | T | 1 | a0017 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.1063G>A | p.Gly355Arg | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 6/13 | 1176/3149 | 1063/2010 | 355/669 | chr12 | 6355352 | |||
| chr12:6355415 | C | T | 5 | a0003 a0005 a0006 others(2): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
missense_variant | MODERATE | c.1000G>A | p.Ala334Thr | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 6/13 | 1113/3149 | 1000/2010 | 334/669 | chr12 | 6355415 | |||
| chr12:6363513 | C | T | 1 | a0010 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.614G>A | p.Ser205Asn | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/13 | 727/3149 | 614/2010 | 205/669 | chr12 | 6363513 | |||
| chr12:6363586 | G | A | 1 | a0008 | 2 | HG01074.hp2 HG03710.hp2 |
missense_variant | MODERATE | c.541C>T | p.Arg181Trp | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/13 | 654/3149 | 541/2010 | 181/669 | chr12 | 6363586 | |||
| chr12:6374641 | A | C | 1 | a0009 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.143T>G | p.Leu48Arg | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/13 | 256/3149 | 143/2010 | 48/669 | chr12 | 6374641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6348964 | G | A | 1 | a0003c0018 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.1539C>T | p.Thr513Thr | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 11/13 | 1652/3149 | 1539/2010 | 513/669 | chr12 | 6348964 | |||
| chr12:6349176 | C | A | 4 | a0001c0029 a0002c0028 a0004c0012 others(1): Show |
10 | NA18944.hp2 NA18945.hp1 NA18973.hp2 others(7): Show |
synonymous_variant | LOW | c.1485G>T | p.Ser495Ser | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/13 | 1598/3149 | 1485/2010 | 495/669 | chr12 | 6349176 | |||
| chr12:6355778 | G | A | 1 | a0001c0004 | 10 | HG02258.hp2 HG02559.hp1 HG02886.hp2 others(7): Show |
splice_region_variant&synonymous_variant | LOW | c.978C>T | p.Asn326Asn | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 5/13 | 1091/3149 | 978/2010 | 326/669 | chr12 | 6355778 | |||
| chr12:6363587 | C | A | 1 | a0008c0015 | 2 | HG01074.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.540G>T | p.Leu180Leu | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/13 | 653/3149 | 540/2010 | 180/669 | chr12 | 6363587 | |||
| chr12:6374685 | G | A | 10 | a0001c0006 a0001c0029 a0002c0011 others(7): Show |
30 | HG00438.hp2 HG02132.hp1 HG02132.hp2 others(27): Show |
synonymous_variant | LOW | c.99C>T | p.Pro33Pro | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/13 | 212/3149 | 99/2010 | 33/669 | chr12 | 6374685 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6346853 | CAACA | C | 9 | a0001c0001t0003 a0002c0028t0003 a0003c0003t0006 others(6): Show |
25 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1016_*1019delTGTT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 1016 | chr12 | 6346853 | ||||||
| chr12:6346885 | C | G | 1 | a0001c0001t0015 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 988 | chr12 | 6346885 | ||||||
| chr12:6346909 | C | T | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*964G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 964 | chr12 | 6346909 | ||||||
| chr12:6347240 | C | A | 1 | a0001c0001t0016 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*633G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 633 | chr12 | 6347240 | ||||||
| chr12:6347364 | A | C | 2 | a0002c0002t0007 a0002c0002t0010 |
4 | HG02155.hp1 NA18963.hp2 NA18969.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*509T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 509 | chr12 | 6347364 | ||||||
| chr12:6347537 | C | T | 2 | a0004c0009t0008 a0006c0005t0008 |
2 | HG02630.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*336G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 336 | chr12 | 6347537 | ||||||
| chr12:6347577 | G | A | 1 | a0008c0015t0017 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 296 | chr12 | 6347577 | ||||||
| chr12:6347615 | T | C | 1 | a0002c0002t0018 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*258A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 258 | chr12 | 6347615 | ||||||
| chr12:6347669 | G | C | 1 | a0001c0001t0011 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 204 | chr12 | 6347669 | ||||||
| chr12:6347739 | G | A | 1 | a0001c0006t0019 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 134 | chr12 | 6347739 | ||||||
| chr12:6347760 | G | A | 1 | a0002c0002t0012 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 113 | chr12 | 6347760 | ||||||
| chr12:6347803 | A | G | 3 | a0001c0001t0009 a0001c0001t0013 a0003c0003t0006 |
5 | HG01192.hp2 HG01884.hp1 NA19011.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*70T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 13/13 | 70 | chr12 | 6347803 | ||||||
| chr12:6374811 | A | G | 2 | a0001c0001t0005 a0003c0003t0005 |
4 | HG02723.hp1 HG03453.hp1 NA18522.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-28T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/13 | 28 | chr12 | 6374811 | ||||||
| chr12:6374831 | T | C | 4 | a0001c0001t0004 a0001c0004t0004 a0002c0002t0004 others(1): Show |
5 | HG02055.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-48A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/13 | 48 | chr12 | 6374831 | ||||||
| chr12:6375543 | T | C | 47 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(44): Show |
370 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(367): Show |
5_prime_UTR_variant | MODIFIER | c.-93A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/13 | 760 | chr12 | 6375543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6348273 | T | C | 1 | a0011c0022t0001g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1630-20A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348273 | |||||||
| chr12:6348404 | G | C | 1 | a0001c0001t0001g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1630-151C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348404 | |||||||
| chr12:6348489 | C | A | 1 | a0002c0002t0001g0162 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1630-236G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348489 | |||||||
| chr12:6348632 | C | T | 1 | a0001c0001t0001g0369 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1629+95G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348632 | |||||||
| chr12:6348664 | C | T | 23 | a0001c0001t0001g0023 a0001c0001t0001g0155 a0001c0001t0001g0199 others(20): Show |
24 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1629+63G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348664 | |||||||
| chr12:6348670 | C | A | 31 | a0001c0001t0001g0023 a0001c0001t0001g0155 a0001c0001t0001g0199 others(28): Show |
34 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(31): Show |
intron_variant | MODIFIER | c.1629+57G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348670 | |||||||
| chr12:6348676 | T | C | 6 | a0001c0001t0001g0133 a0001c0001t0014g0274 a0003c0003t0001g0234 others(3): Show |
6 | HG01952.hp1 HG02258.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1629+51A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348676 | |||||||
| chr12:6348699 | T | A | 1 | a0001c0001t0002g0084 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1629+28A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 12/12 | chr12 | 6348699 | |||||||
| chr12:6348877 | C | T | 6 | a0003c0003t0001g0168 a0003c0003t0001g0245 a0003c0003t0001g0284 others(3): Show |
6 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1553+73G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 11/12 | chr12 | 6348877 | |||||||
| chr12:6348918 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(283): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.1553+32G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 11/12 | chr12 | 6348918 | |||||||
| chr12:6349105 | A | G | 1 | a0003c0010t0001g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1497+59T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/12 | chr12 | 6349105 | |||||||
| chr12:6349108 | G | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0001t0001g0144 others(64): Show |
73 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1497+56C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/12 | chr12 | 6349108 | |||||||
| chr12:6349122 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1497+42A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/12 | chr12 | 6349122 | |||||||
| chr12:6349145 | T | A | 1 | a0002c0002t0001g0396 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1497+19A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/12 | chr12 | 6349145 | |||||||
| chr12:6349158 | C | G | 1 | a0003c0010t0001g0118 | 1 | NA18612.hp1 | splice_region_variant&intron_variant | LOW | c.1497+6G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 10/12 | chr12 | 6349158 | |||||||
| chr12:6349279 | G | A | 1 | a0002c0002t0001g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1439+48C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 9/12 | chr12 | 6349279 | |||||||
| chr12:6349279 | G | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0229 a0001c0001t0001g0354 others(1): Show |
5 | HG02280.hp1 HG02280.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1439+48C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 9/12 | chr12 | 6349279 | |||||||
| chr12:6349537 | G | A | 49 | a0001c0001t0001g0158 a0001c0001t0001g0270 a0001c0001t0001g0271 others(46): Show |
50 | HG01109.hp2 HG01192.hp2 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.1361-132C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349537 | |||||||
| chr12:6349667 | C | G | 1 | a0002c0002t0001g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1361-262G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349667 | |||||||
| chr12:6349720 | A | T | 1 | a0006c0005t0003g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-315T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349720 | |||||||
| chr12:6349725 | T | A | 2 | a0001c0029t0001g0112 a0004c0014t0003g0128 |
2 | NA18944.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1361-320A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349725 | |||||||
| chr12:6349758 | G | A | 1 | a0002c0002t0007g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1361-353C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349758 | |||||||
| chr12:6349775 | A | G | 1 | a0001c0001t0001g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1361-370T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349775 | |||||||
| chr12:6349791 | A | G | 16 | a0001c0001t0001g0023 a0001c0001t0001g0211 a0001c0001t0001g0218 others(13): Show |
17 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1361-386T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349791 | |||||||
| chr12:6349827 | T | C | 7 | a0001c0001t0014g0274 a0003c0003t0001g0237 a0003c0003t0001g0282 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-422A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349827 | |||||||
| chr12:6349828 | A | G | 7 | a0001c0001t0014g0274 a0003c0003t0001g0237 a0003c0003t0001g0282 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-423T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349828 | |||||||
| chr12:6349938 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1361-533T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6349938 | |||||||
| chr12:6350159 | G | A | 1 | a0008c0015t0001g0382 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1361-754C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350159 | |||||||
| chr12:6350160 | T | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(259): Show |
299 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1361-755A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350160 | |||||||
| chr12:6350161 | G | A | 2 | a0001c0001t0001g0387 a0002c0002t0002g0055 |
2 | HG02040.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1361-756C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350161 | |||||||
| chr12:6350171 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1361-766C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350171 | |||||||
| chr12:6350204 | G | A | 1 | a0003c0003t0001g0302 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1361-799C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350204 | |||||||
| chr12:6350204 | G | T | 1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1361-799C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350204 | |||||||
| chr12:6350207 | T | C | 1 | a0003c0003t0001g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1361-802A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350207 | |||||||
| chr12:6350214 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1361-809G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350214 | |||||||
| chr12:6350222 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1361-817T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350222 | |||||||
| chr12:6350259 | C | T | 1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1361-854G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350259 | |||||||
| chr12:6350281 | AAT | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0211 a0001c0001t0001g0218 others(2): Show |
6 | HG02615.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361-878_1361-877d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350281 | |||||||
| chr12:6350293 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1361-888C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350293 | |||||||
| chr12:6350299 | G | A | 1 | a0002c0002t0002g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1361-894C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350299 | |||||||
| chr12:6350322 | C | T | 1 | a0003c0003t0001g0281 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1361-917G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350322 | |||||||
| chr12:6350381 | G | C | 1 | a0003c0010t0001g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1361-976C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350381 | |||||||
| chr12:6350393 | T | C | 3 | a0003c0003t0001g0029 a0003c0003t0001g0102 a0003c0003t0001g0411 |
4 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-988A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350393 | |||||||
| chr12:6350421 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1361-1016C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350421 | |||||||
| chr12:6350433 | C | CA | 10 | a0001c0001t0001g0261 a0002c0002t0001g0018 a0002c0002t0001g0372 others(7): Show |
11 | HG00621.hp2 HG01952.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-1029dupT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350433 | |||||||
| chr12:6350433 | CA | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0177 a0001c0001t0001g0211 others(10): Show |
14 | HG02615.hp2 HG02897.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.1361-1029delT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350433 | |||||||
| chr12:6350574 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1361-1169G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350574 | |||||||
| chr12:6350734 | G | A | 3 | a0003c0003t0001g0233 a0003c0003t0001g0240 a0003c0003t0001g0242 |
3 | HG01358.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1361-1329C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350734 | |||||||
| chr12:6350844 | T | TAATA | 6 | a0001c0001t0001g0154 a0001c0001t0001g0290 a0001c0001t0001g0361 others(3): Show |
9 | HG00423.hp1 HG04115.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-1443_1361-144 others(8): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350844 | |||||||
| chr12:6350844 | TAATA | T | 59 | a0001c0001t0001g0155 a0001c0001t0001g0270 a0001c0001t0001g0271 others(56): Show |
60 | HG01109.hp2 HG01192.hp2 HG01358.hp2 others(57): Show |
intron_variant | MODIFIER | c.1361-1443_1361-144 others(8): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350844 | |||||||
| chr12:6350844 | TAATAAAT others(1): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0211 a0001c0001t0001g0294 others(4): Show |
12 | HG03471.hp1 NA18940.hp1 NA18964.hp2 others(9): Show |
intron_variant | MODIFIER | c.1361-1447_1361-144 others(12): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350844 | |||||||
| chr12:6350925 | C | A | 4 | a0004c0009t0003g0335 a0004c0012t0003g0333 a0004c0012t0003g0336 others(1): Show |
4 | NA18970.hp2 NA18994.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-1520G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6350925 | |||||||
| chr12:6351070 | C | T | 1 | a0002c0002t0001g0396 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1361-1665G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351070 | |||||||
| chr12:6351250 | C | T | 1 | a0002c0002t0001g0391 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1361-1845G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351250 | |||||||
| chr12:6351332 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-1927C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351332 | |||||||
| chr12:6351478 | C | T | 2 | a0001c0001t0001g0356 a0006c0005t0003g0156 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1361-2073G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351478 | |||||||
| chr12:6351496 | G | A | 1 | a0003c0003t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1361-2091C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351496 | |||||||
| chr12:6351498 | C | T | 1 | a0001c0001t0001g0389 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1361-2093G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351498 | |||||||
| chr12:6351500 | G | T | 1 | a0015c0027t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1361-2095C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351500 | |||||||
| chr12:6351635 | A | G | 1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1361-2230T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351635 | |||||||
| chr12:6351689 | C | T | 5 | a0003c0003t0001g0237 a0003c0003t0001g0282 a0006c0005t0003g0136 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-2284G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351689 | |||||||
| chr12:6351766 | A | C | 1 | a0006c0005t0003g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1361-2361T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351766 | |||||||
| chr12:6351772 | TTATC | T | 57 | a0001c0001t0001g0155 a0001c0001t0001g0270 a0001c0001t0001g0271 others(54): Show |
58 | HG01109.hp2 HG01192.hp2 HG01358.hp2 others(55): Show |
intron_variant | MODIFIER | c.1361-2371_1361-236 others(8): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351772 | |||||||
| chr12:6351865 | T | G | 2 | a0003c0003t0001g0234 a0003c0003t0001g0304 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1361-2460A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351865 | |||||||
| chr12:6351921 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1361-2516T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6351921 | |||||||
| chr12:6352021 | G | T | 1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1360+2417C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352021 | |||||||
| chr12:6352036 | C | T | 1 | a0003c0003t0001g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1360+2402G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352036 | |||||||
| chr12:6352063 | G | A | 58 | a0001c0001t0001g0155 a0001c0001t0001g0270 a0001c0001t0001g0271 others(55): Show |
59 | HG01109.hp2 HG01192.hp2 HG01358.hp2 others(56): Show |
intron_variant | MODIFIER | c.1360+2375C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352063 | |||||||
| chr12:6352198 | A | T | 1 | a0003c0010t0001g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1360+2240T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352198 | |||||||
| chr12:6352237 | A | AAAT | 50 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0311 others(47): Show |
51 | HG01109.hp2 HG01192.hp2 HG01358.hp2 others(48): Show |
intron_variant | MODIFIER | c.1360+2198_1360+220 others(7): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352237 | |||||||
| chr12:6352609 | T | C | 6 | a0001c0001t0001g0155 a0001c0001t0001g0340 a0001c0001t0001g0345 others(3): Show |
6 | HG01891.hp2 HG01993.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+1829A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352609 | |||||||
| chr12:6352833 | G | A | 2 | a0001c0004t0001g0016 a0001c0004t0001g0208 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1360+1605C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352833 | |||||||
| chr12:6352860 | T | C | 1 | a0003c0003t0001g0302 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1360+1578A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352860 | |||||||
| chr12:6352878 | G | A | 1 | a0003c0010t0001g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1360+1560C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352878 | |||||||
| chr12:6352923 | C | T | 1 | a0010c0017t0001g0344 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1360+1515G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6352923 | |||||||
| chr12:6353026 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1360+1412C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353026 | |||||||
| chr12:6353036 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1360+1402A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353036 | |||||||
| chr12:6353231 | TA | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(105): Show |
128 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1360+1206delT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353231 | |||||||
| chr12:6353447 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0026 others(77): Show |
94 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1360+991C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353447 | |||||||
| chr12:6353506 | T | C | 1 | a0004c0009t0003g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1360+932A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353506 | |||||||
| chr12:6353514 | C | A | 1 | a0001c0001t0001g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1360+924G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353514 | |||||||
| chr12:6353516 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1360+922C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353516 | |||||||
| chr12:6353600 | A | T | 2 | a0001c0001t0001g0211 a0002c0002t0001g0272 |
2 | HG02015.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1360+838T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353600 | |||||||
| chr12:6353604 | T | A | 41 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0158 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.1360+834A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353604 | |||||||
| chr12:6353622 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(294): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1360+816G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353622 | |||||||
| chr12:6353628 | C | T | 1 | a0001c0004t0001g0409 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1360+810G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353628 | |||||||
| chr12:6353629 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(296): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1360+809T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353629 | |||||||
| chr12:6353642 | T | G | 7 | a0001c0001t0001g0150 a0001c0001t0001g0384 a0001c0001t0002g0044 others(4): Show |
7 | HG00280.hp1 HG00642.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1360+796A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353642 | |||||||
| chr12:6353646 | A | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(295): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1360+792T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353646 | |||||||
| chr12:6353651 | G | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(279): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.1360+787C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353651 | |||||||
| chr12:6353652 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(292): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1360+786A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353652 | |||||||
| chr12:6353652 | T | G | 3 | a0001c0001t0001g0345 a0003c0003t0001g0276 a0003c0003t0001g0408 |
3 | HG01891.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1360+786A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353652 | |||||||
| chr12:6353659 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(296): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1360+779T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353659 | |||||||
| chr12:6353670 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1360+768C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353670 | |||||||
| chr12:6353679 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(265): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1360+759A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353679 | |||||||
| chr12:6353682 | C | CG | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(265): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1360+755dupC | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353682 | |||||||
| chr12:6353687 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(294): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1360+751G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353687 | |||||||
| chr12:6353691 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(294): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1360+747T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353691 | |||||||
| chr12:6353738 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1360+700G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353738 | |||||||
| chr12:6353745 | T | A | 9 | a0001c0001t0001g0132 a0003c0003t0001g0198 a0003c0003t0001g0233 others(6): Show |
9 | HG01358.hp2 HG01952.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+693A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353745 | |||||||
| chr12:6353750 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1360+688G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353750 | |||||||
| chr12:6353751 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1360+687C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353751 | |||||||
| chr12:6353765 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0294 a0001c0001t0001g0313 others(2): Show |
10 | NA18940.hp1 NA18964.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1360+673T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353765 | |||||||
| chr12:6353779 | C | CG | 5 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0002c0002t0001g0159 others(2): Show |
5 | HG03225.hp2 NA18944.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+658dupC | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353779 | |||||||
| chr12:6353779 | C | T | 6 | a0001c0001t0001g0402 a0001c0001t0002g0084 a0001c0001t0002g0088 others(3): Show |
6 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+659G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353779 | |||||||
| chr12:6353780 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0133 others(124): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1360+658C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353780 | |||||||
| chr12:6353790 | C | A | 1 | a0008c0015t0001g0382 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1360+648G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353790 | |||||||
| chr12:6353790 | C | T | 10 | a0001c0001t0001g0215 a0001c0001t0001g0402 a0001c0001t0002g0064 others(7): Show |
11 | HG00438.hp2 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360+648G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353790 | |||||||
| chr12:6353791 | G | A | 6 | a0001c0001t0001g0381 a0001c0006t0001g0113 a0003c0003t0001g0185 others(3): Show |
6 | HG03834.hp1 HG03942.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1360+647C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353791 | |||||||
| chr12:6353796 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1360+642T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353796 | |||||||
| chr12:6353800 | A | AG | 5 | a0001c0004t0001g0207 a0001c0004t0001g0275 a0001c0004t0001g0323 others(2): Show |
5 | HG02258.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+637dupC | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353800 | |||||||
| chr12:6353802 | G | A | 1 | a0002c0002t0001g0021 | 2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1360+636C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353802 | |||||||
| chr12:6353803 | A | G | 31 | a0001c0001t0001g0025 a0001c0001t0001g0211 a0001c0001t0001g0229 others(28): Show |
33 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1360+635T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353803 | |||||||
| chr12:6353805 | G | A | 15 | a0001c0001t0001g0199 a0001c0001t0001g0320 a0001c0001t0001g0357 others(12): Show |
15 | HG02109.hp1 HG02572.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1360+633C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353805 | |||||||
| chr12:6353808 | C | T | 1 | a0008c0015t0001g0382 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1360+630G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353808 | |||||||
| chr12:6353810 | C | T | 1 | a0006c0005t0003g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1360+628G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353810 | |||||||
| chr12:6353811 | C | A | 2 | a0001c0001t0001g0384 a0002c0002t0001g0203 |
2 | HG01346.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1360+627G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353811 | |||||||
| chr12:6353811 | C | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(302): Show |
336 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.1360+627G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353811 | |||||||
| chr12:6353811 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1360+627G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353811 | |||||||
| chr12:6353813 | T | C | 2 | a0001c0001t0011g0101 a0002c0002t0001g0151 |
2 | HG00597.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1360+625A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353813 | |||||||
| chr12:6353814 | C | A | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1360+624G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353814 | |||||||
| chr12:6353824 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1360+614G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353824 | |||||||
| chr12:6353832 | G | A | 19 | a0001c0001t0001g0155 a0001c0001t0001g0199 a0001c0001t0001g0219 others(16): Show |
19 | HG02015.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1360+606C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353832 | |||||||
| chr12:6353836 | G | A | 1 | a0002c0011t0001g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1360+602C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353836 | |||||||
| chr12:6353836 | G | T | 1 | a0001c0001t0014g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1360+602C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353836 | |||||||
| chr12:6353839 | G | T | 19 | a0001c0001t0001g0155 a0001c0001t0001g0199 a0001c0001t0001g0219 others(16): Show |
19 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1360+599C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353839 | |||||||
| chr12:6353840 | T | C | 18 | a0001c0001t0001g0155 a0001c0001t0001g0199 a0001c0001t0001g0219 others(15): Show |
18 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1360+598A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353840 | |||||||
| chr12:6353841 | G | A | 2 | a0001c0001t0001g0365 a0001c0001t0014g0274 |
2 | HG03669.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1360+597C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353841 | |||||||
| chr12:6353842 | G | A | 1 | a0001c0006t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1360+596C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353842 | |||||||
| chr12:6353864 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1360+574G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353864 | |||||||
| chr12:6353869 | G | A | 2 | a0001c0001t0001g0373 a0002c0002t0010g0095 |
2 | NA18963.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1360+569C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353869 | |||||||
| chr12:6353874 | C | T | 1 | a0002c0002t0002g0048 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1360+564G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353874 | |||||||
| chr12:6353876 | A | C | 43 | a0001c0001t0001g0025 a0001c0001t0001g0229 a0001c0001t0001g0319 others(40): Show |
46 | HG01109.hp2 HG01192.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.1360+562T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353876 | |||||||
| chr12:6353876 | A | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0280 a0001c0001t0002g0070 others(2): Show |
5 | HG00544.hp2 NA18939.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+562T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353876 | |||||||
| chr12:6353879 | G | A | 1 | a0006c0005t0003g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1360+559C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6353879 | |||||||
| chr12:6354005 | T | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0180 a0001c0001t0001g0181 others(27): Show |
35 | HG00621.hp1 HG02129.hp2 HG02132.hp1 others(32): Show |
intron_variant | MODIFIER | c.1360+433A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354005 | |||||||
| chr12:6354025 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1360+413A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354025 | |||||||
| chr12:6354026 | T | G | 7 | a0001c0004t0001g0016 a0001c0004t0001g0207 a0001c0004t0001g0208 others(4): Show |
8 | HG02258.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360+412A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354026 | |||||||
| chr12:6354040 | C | G | 2 | a0003c0003t0001g0276 a0003c0003t0001g0408 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1360+398G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354040 | |||||||
| chr12:6354103 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0002g0093 |
2 | HG00639.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1360+335A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354103 | |||||||
| chr12:6354111 | G | A | 1 | a0006c0005t0003g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1360+327C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354111 | |||||||
| chr12:6354121 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1360+317A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354121 | |||||||
| chr12:6354161 | G | A | 6 | a0001c0001t0001g0174 a0001c0001t0002g0059 a0001c0001t0002g0062 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+277C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354161 | |||||||
| chr12:6354174 | TGAGCCGA others(4): Show |
T | 3 | a0001c0001t0002g0094 a0002c0002t0001g0220 a0002c0002t0001g0385 |
3 | HG02074.hp2 HG02129.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1360+253_1360+263d others(13): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354174 | |||||||
| chr12:6354179 | C | T | 45 | a0001c0001t0001g0025 a0001c0001t0001g0229 a0001c0001t0001g0319 others(42): Show |
49 | HG01192.hp2 HG01346.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1360+259G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354179 | |||||||
| chr12:6354199 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1360+239G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354199 | |||||||
| chr12:6354204 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1360+234G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354204 | |||||||
| chr12:6354217 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(102): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1360+221G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354217 | |||||||
| chr12:6354391 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0002g0007 a0001c0001t0002g0065 others(1): Show |
5 | HG01168.hp2 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+47C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 8/12 | chr12 | 6354391 | |||||||
| chr12:6354696 | G | A | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(294): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1242+54C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 7/12 | chr12 | 6354696 | |||||||
| chr12:6354710 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1242+40A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 7/12 | chr12 | 6354710 | |||||||
| chr12:6355021 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1144-173G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 6/12 | chr12 | 6355021 | |||||||
| chr12:6355216 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1143+56C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 6/12 | chr12 | 6355216 | |||||||
| chr12:6355238 | C | T | 2 | a0001c0001t0001g0355 a0004c0009t0008g0321 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1143+34G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 6/12 | chr12 | 6355238 | |||||||
| chr12:6355470 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0195 |
2 | NA18984.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.980-35C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 5/12 | chr12 | 6355470 | |||||||
| chr12:6355618 | G | A | 33 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0104 others(30): Show |
38 | HG02129.hp2 HG02132.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.979+159C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 5/12 | chr12 | 6355618 | |||||||
| chr12:6355620 | C | T | 2 | a0002c0002t0001g0399 a0002c0002t0001g0400 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.979+157G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 5/12 | chr12 | 6355620 | |||||||
| chr12:6355643 | C | T | 6 | a0001c0001t0001g0358 a0002c0002t0001g0249 a0002c0002t0001g0312 others(3): Show |
6 | HG00438.hp2 HG02027.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+134G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 5/12 | chr12 | 6355643 | |||||||
| chr12:6355666 | G | A | 1 | a0006c0005t0003g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.979+111C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 5/12 | chr12 | 6355666 | |||||||
| chr12:6356189 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0356 a0013c0023t0003g0359 |
3 | HG01891.hp2 HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.876-309A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356189 | |||||||
| chr12:6356346 | C | T | 2 | a0001c0001t0001g0340 a0001c0001t0002g0091 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.876-466G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356346 | |||||||
| chr12:6356437 | G | GGAAT | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0147 others(16): Show |
21 | HG01257.hp1 HG01433.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.876-561_876-558dup others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356437 | |||||||
| chr12:6356437 | GGAAT | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(173): Show |
191 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.876-561_876-558del others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356437 | |||||||
| chr12:6356437 | GGAATGAA others(1): Show |
G | 9 | a0001c0004t0001g0016 a0001c0004t0001g0207 a0001c0004t0001g0208 others(6): Show |
10 | HG02258.hp2 HG02559.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.876-565_876-558del others(8): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356437 | |||||||
| chr12:6356524 | G | A | 3 | a0003c0003t0001g0276 a0003c0003t0001g0408 a0006c0005t0003g0156 |
3 | HG03486.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.876-644C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356524 | |||||||
| chr12:6356561 | T | C | 114 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0155 others(111): Show |
123 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(120): Show |
intron_variant | MODIFIER | c.876-681A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356561 | |||||||
| chr12:6356714 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.876-834C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356714 | |||||||
| chr12:6356796 | C | T | 1 | a0001c0004t0001g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.876-916G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356796 | |||||||
| chr12:6356797 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(67): Show |
81 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.876-917C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356797 | |||||||
| chr12:6356804 | A | G | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(308): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.876-924T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356804 | |||||||
| chr12:6356813 | C | T | 1 | a0002c0002t0001g0371 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.876-933G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356813 | |||||||
| chr12:6356889 | G | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(106): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.876-1009C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356889 | |||||||
| chr12:6356915 | A | G | 102 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(99): Show |
109 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(106): Show |
intron_variant | MODIFIER | c.876-1035T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356915 | |||||||
| chr12:6356979 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.876-1099C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6356979 | |||||||
| chr12:6357170 | G | A | 1 | a0003c0003t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.876-1290C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357170 | |||||||
| chr12:6357193 | A | T | 1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.876-1313T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357193 | |||||||
| chr12:6357205 | T | C | 114 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0155 others(111): Show |
123 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(120): Show |
intron_variant | MODIFIER | c.876-1325A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357205 | |||||||
| chr12:6357224 | C | T | 1 | a0018c0024t0001g0202 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.876-1344G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357224 | |||||||
| chr12:6357252 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.876-1372G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357252 | |||||||
| chr12:6357466 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0144 others(78): Show |
88 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.876-1586G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357466 | |||||||
| chr12:6357547 | C | T | 1 | a0002c0002t0002g0048 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.876-1667G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357547 | |||||||
| chr12:6357555 | C | CAA | 104 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(101): Show |
111 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(108): Show |
intron_variant | MODIFIER | c.876-1677_876-1676d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357555 | |||||||
| chr12:6357575 | G | A | 105 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(102): Show |
112 | HG00544.hp1 HG00621.hp1 HG01109.hp2 others(109): Show |
intron_variant | MODIFIER | c.876-1695C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357575 | |||||||
| chr12:6357735 | C | T | 2 | a0006c0005t0003g0136 a0006c0005t0003g0353 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.876-1855G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357735 | |||||||
| chr12:6357855 | G | A | 1 | a0003c0018t0001g0267 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.876-1975C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357855 | |||||||
| chr12:6357901 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.876-2021C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357901 | |||||||
| chr12:6357956 | C | A | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.876-2076G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6357956 | |||||||
| chr12:6358107 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.876-2227G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358107 | |||||||
| chr12:6358123 | C | T | 2 | a0003c0003t0001g0103 a0003c0003t0001g0212 |
2 | HG01346.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.876-2243G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358123 | |||||||
| chr12:6358138 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.876-2258C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358138 | |||||||
| chr12:6358234 | T | A | 1 | a0002c0002t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.876-2354A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358234 | |||||||
| chr12:6358280 | C | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(297): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.876-2400G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358280 | |||||||
| chr12:6358319 | T | C | 1 | a0001c0001t0014g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.876-2439A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358319 | |||||||
| chr12:6358323 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0001g0361 a0002c0002t0001g0209 others(1): Show |
4 | HG00423.hp1 HG02056.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-2443A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358323 | |||||||
| chr12:6358402 | C | G | 6 | a0001c0001t0001g0358 a0002c0002t0001g0249 a0002c0002t0001g0312 others(3): Show |
6 | HG00438.hp2 HG02027.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-2522G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358402 | |||||||
| chr12:6358412 | C | T | 21 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(18): Show |
22 | HG00621.hp1 HG01993.hp2 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.876-2532G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358412 | |||||||
| chr12:6358527 | T | C | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.876-2647A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358527 | |||||||
| chr12:6358597 | AC | A | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.876-2718delG | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358597 | |||||||
| chr12:6358656 | C | T | 4 | a0001c0001t0001g0210 a0001c0001t0001g0361 a0002c0002t0001g0209 others(1): Show |
4 | HG00423.hp1 HG02056.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-2776G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358656 | |||||||
| chr12:6358669 | G | A | 21 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(18): Show |
22 | HG00621.hp1 HG01993.hp2 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.876-2789C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358669 | |||||||
| chr12:6358795 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(299): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.876-2915T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358795 | |||||||
| chr12:6358852 | C | T | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.876-2972G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358852 | |||||||
| chr12:6358859 | C | CA | 18 | a0001c0001t0001g0142 a0001c0001t0001g0161 a0001c0001t0001g0172 others(15): Show |
21 | HG00597.hp2 HG01257.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.876-2980dupT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358859 | |||||||
| chr12:6358859 | CA | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(95): Show |
108 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.876-2980delT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358859 | |||||||
| chr12:6358859 | CAA | C | 76 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(73): Show |
82 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(79): Show |
intron_variant | MODIFIER | c.876-2981_876-2980d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6358859 | |||||||
| chr12:6359039 | C | T | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.875+3012G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359039 | |||||||
| chr12:6359137 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(181): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.875+2914A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359137 | |||||||
| chr12:6359170 | T | G | 1 | a0002c0002t0002g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.875+2881A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359170 | |||||||
| chr12:6359173 | TAATGGTT others(4): Show |
T | 1 | a0002c0002t0002g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.875+2867_875+2877d others(13): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359173 | |||||||
| chr12:6359274 | A | T | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.875+2777T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359274 | |||||||
| chr12:6359289 | G | A | 79 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(76): Show |
85 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(82): Show |
intron_variant | MODIFIER | c.875+2762C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359289 | |||||||
| chr12:6359302 | G | A | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.875+2749C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359302 | |||||||
| chr12:6359349 | T | C | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(300): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.875+2702A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359349 | |||||||
| chr12:6359760 | A | G | 1 | a0003c0003t0001g0342 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.875+2291T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359760 | |||||||
| chr12:6359764 | C | CT | 13 | a0001c0001t0001g0147 a0001c0001t0001g0195 a0001c0001t0001g0280 others(10): Show |
13 | HG00597.hp2 HG00673.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.875+2286dupA | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359764 | C | CTT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.875+2285_875+2286d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359764 | C | CTTT | 11 | a0001c0001t0001g0153 a0001c0001t0001g0167 a0001c0001t0001g0287 others(8): Show |
11 | HG01515.hp2 HG02135.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.875+2284_875+2286d others(5): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359764 | CT | C | 58 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(55): Show |
60 | HG00544.hp1 HG00621.hp1 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.875+2286delA | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359764 | CTT | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(97): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.875+2285_875+2286d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359764 | CTTT | C | 11 | a0001c0001t0001g0268 a0003c0003t0001g0006 a0003c0003t0001g0020 others(8): Show |
14 | HG02129.hp2 NA18612.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.875+2284_875+2286d others(5): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359764 | CTTTT | C | 31 | a0003c0003t0001g0104 a0003c0003t0001g0165 a0003c0003t0001g0166 others(28): Show |
33 | HG01167.hp2 HG01169.hp1 HG02132.hp1 others(30): Show |
intron_variant | MODIFIER | c.875+2283_875+2286d others(6): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359764 | |||||||
| chr12:6359788 | T | C | 1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.875+2263A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359788 | |||||||
| chr12:6359932 | G | A | 1 | a0003c0003t0001g0351 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.875+2119C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6359932 | |||||||
| chr12:6360200 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0002g0001 a0001c0001t0002g0050 others(2): Show |
10 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.875+1851C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360200 | |||||||
| chr12:6360227 | G | T | 1 | a0001c0001t0003g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.875+1824C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360227 | |||||||
| chr12:6360250 | C | A | 22 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(19): Show |
23 | HG00621.hp1 HG01993.hp2 HG02698.hp2 others(20): Show |
intron_variant | MODIFIER | c.875+1801G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360250 | |||||||
| chr12:6360276 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.875+1775C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360276 | |||||||
| chr12:6360505 | G | T | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(297): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.875+1546C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360505 | |||||||
| chr12:6360596 | G | A | 1 | a0003c0003t0001g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.875+1455C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360596 | |||||||
| chr12:6360719 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0229 a0001c0001t0001g0340 others(7): Show |
12 | HG02145.hp1 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+1332G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360719 | |||||||
| chr12:6360731 | G | C | 78 | a0003c0003t0001g0006 a0003c0003t0001g0020 a0003c0003t0001g0029 others(75): Show |
84 | HG00544.hp1 HG01109.hp2 HG01167.hp2 others(81): Show |
intron_variant | MODIFIER | c.875+1320C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360731 | |||||||
| chr12:6360781 | A | AC | 110 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(107): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.875+1269dupG | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360781 | |||||||
| chr12:6360783 | C | A | 1 | a0003c0003t0001g0029 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.875+1268G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360783 | |||||||
| chr12:6360838 | T | C | 4 | a0001c0001t0001g0287 a0001c0001t0001g0367 a0001c0001t0001g0376 others(1): Show |
4 | HG00597.hp1 NA18939.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+1213A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360838 | |||||||
| chr12:6360861 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.875+1190C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360861 | |||||||
| chr12:6360897 | G | A | 1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.875+1154C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6360897 | |||||||
| chr12:6361004 | C | T | 9 | a0003c0003t0001g0198 a0003c0003t0001g0233 a0003c0003t0001g0240 others(6): Show |
9 | HG01261.hp1 HG01358.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.875+1047G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361004 | |||||||
| chr12:6361011 | G | C | 1 | a0002c0002t0001g0193 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.875+1040C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361011 | |||||||
| chr12:6361094 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(226): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.875+957T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361094 | |||||||
| chr12:6361186 | C | T | 1 | a0006c0005t0003g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.875+865G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361186 | |||||||
| chr12:6361447 | A | C | 4 | a0001c0001t0001g0219 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
4 | HG01891.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+604T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361447 | |||||||
| chr12:6361477 | C | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0065 |
3 | HG01168.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.875+574G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361477 | |||||||
| chr12:6361639 | A | G | 1 | a0006c0005t0003g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.875+412T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361639 | |||||||
| chr12:6361758 | C | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(98): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.875+293G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361758 | |||||||
| chr12:6361905 | C | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(103): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.875+146G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361905 | |||||||
| chr12:6361976 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.875+75C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361976 | |||||||
| chr12:6361980 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.875+71T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6361980 | |||||||
| chr12:6362024 | G | A | 1 | a0003c0003t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.875+27C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 4/12 | chr12 | 6362024 | |||||||
| chr12:6362280 | G | A | 1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.685-39C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362280 | |||||||
| chr12:6362328 | G | A | 1 | a0006c0005t0003g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.685-87C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362328 | |||||||
| chr12:6362710 | C | T | 2 | a0001c0001t0001g0345 a0001c0001t0001g0356 |
2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.685-469G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362710 | |||||||
| chr12:6362853 | AT | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(202): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.684+589delA | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362853 | |||||||
| chr12:6362935 | G | GGCCTCCC others(631): Show |
2 | a0003c0003t0001g0276 a0003c0003t0001g0408 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.684+507_684+508ins others(638): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(628): Show |
1 | a0003c0003t0001g0306 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(635): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(629): Show |
6 | a0003c0003t0001g0245 a0003c0003t0001g0284 a0003c0003t0001g0342 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(636): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(633): Show |
1 | a0001c0001t0001g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.684+507_684+508ins others(640): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(632): Show |
7 | a0001c0001t0001g0028 a0001c0001t0001g0180 a0001c0001t0001g0187 others(4): Show |
8 | HG01993.hp2 HG02698.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(639): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(631): Show |
10 | a0001c0001t0001g0239 a0001c0001t0001g0311 a0001c0001t0001g0337 others(7): Show |
10 | HG01884.hp2 HG02965.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(638): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(630): Show |
105 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(102): Show |
116 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(637): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(629): Show |
73 | a0001c0001t0001g0023 a0001c0001t0001g0218 a0001c0001t0001g0219 others(70): Show |
80 | HG00423.hp1 HG00544.hp1 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(636): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(631): Show |
1 | a0003c0003t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(638): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(630): Show |
8 | a0001c0001t0001g0155 a0003c0003t0001g0233 a0003c0003t0001g0242 others(5): Show |
8 | HG01261.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(637): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(629): Show |
2 | a0001c0001t0001g0229 a0003c0003t0001g0198 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.684+507_684+508ins others(636): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(628): Show |
1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.684+507_684+508ins others(635): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(629): Show |
1 | a0003c0003t0001g0282 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(636): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(632): Show |
1 | a0001c0001t0001g0315 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(639): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(633): Show |
2 | a0001c0001t0001g0340 a0001c0001t0002g0091 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.684+507_684+508ins others(640): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(631): Show |
8 | a0001c0001t0001g0025 a0001c0001t0001g0341 a0001c0001t0001g0354 others(5): Show |
10 | HG02280.hp2 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(638): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(633): Show |
1 | a0013c0023t0003g0359 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684+507_684+508ins others(640): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(632): Show |
6 | a0001c0001t0001g0329 a0001c0001t0001g0356 a0001c0001t0001g0381 others(3): Show |
6 | HG00597.hp1 HG01978.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(639): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(631): Show |
1 | a0004c0009t0003g0331 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.684+507_684+508ins others(638): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(630): Show |
8 | a0001c0001t0001g0211 a0001c0001t0001g0268 a0001c0001t0001g0310 others(5): Show |
8 | HG01070.hp2 HG01167.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+507_684+508ins others(637): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(629): Show |
1 | a0001c0001t0014g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(636): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(630): Show |
1 | a0001c0001t0001g0377 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(637): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(631): Show |
1 | a0001c0001t0001g0259 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.684+507_684+508ins others(638): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6362935 | G | GGCCTCCC others(629): Show |
1 | a0004c0009t0003g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.684+507_684+508ins others(636): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6362935 | |||||||
| chr12:6363014 | C | G | 1 | a0003c0003t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684+429G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6363014 | |||||||
| chr12:6363138 | C | CAAT | 3 | a0001c0001t0002g0092 a0002c0002t0001g0170 a0002c0002t0001g0251 |
3 | HG00609.hp1 HG02148.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.684+302_684+304dup others(3): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6363138 | |||||||
| chr12:6363138 | CAAT | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0174 others(121): Show |
138 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.684+302_684+304del others(3): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6363138 | |||||||
| chr12:6363297 | C | CT | 7 | a0001c0001t0001g0219 a0001c0001t0001g0325 a0001c0001t0002g0050 others(4): Show |
7 | HG00639.hp1 HG03098.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+145dupA | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6363297 | |||||||
| chr12:6363345 | G | C | 6 | a0001c0001t0004g0406 a0001c0001t0004g0407 a0001c0001t0015g0137 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+98C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 3/12 | chr12 | 6363345 | |||||||
| chr12:6363745 | G | T | 1 | a0001c0004t0004g0404 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.417-35C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6363745 | |||||||
| chr12:6363766 | C | T | 1 | a0003c0003t0001g0411 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.417-56G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6363766 | |||||||
| chr12:6363805 | C | T | 13 | a0001c0001t0001g0155 a0001c0001t0015g0137 a0001c0004t0001g0016 others(10): Show |
15 | HG02572.hp2 HG02886.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.417-95G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6363805 | |||||||
| chr12:6363864 | C | A | 15 | a0001c0001t0003g0225 a0001c0001t0004g0406 a0002c0002t0001g0157 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.417-154G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6363864 | |||||||
| chr12:6364133 | C | A | 1 | a0003c0003t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.417-423G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364133 | |||||||
| chr12:6364174 | C | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0357 a0001c0001t0001g0360 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.417-464G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364174 | |||||||
| chr12:6364383 | C | A | 109 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(106): Show |
118 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.417-673G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364383 | |||||||
| chr12:6364454 | A | C | 13 | a0001c0001t0004g0406 a0002c0002t0001g0157 a0002c0002t0001g0272 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.417-744T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364454 | |||||||
| chr12:6364499 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.417-789A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364499 | |||||||
| chr12:6364541 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.417-831C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364541 | |||||||
| chr12:6364591 | T | TA | 6 | a0001c0001t0001g0199 a0001c0001t0001g0357 a0001c0001t0001g0360 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.417-882dupT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364591 | |||||||
| chr12:6364694 | A | G | 159 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(156): Show |
170 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.417-984T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364694 | |||||||
| chr12:6364713 | G | A | 1 | a0001c0001t0001g0383 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.417-1003C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364713 | |||||||
| chr12:6364729 | T | G | 1 | a0003c0010t0001g0120 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.417-1019A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364729 | |||||||
| chr12:6364744 | A | G | 1 | a0002c0002t0001g0279 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.417-1034T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364744 | |||||||
| chr12:6364761 | CA | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(189): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.417-1052delT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364761 | |||||||
| chr12:6364768 | A | AAC | 108 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(105): Show |
117 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.417-1059_417-1058i others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364768 | |||||||
| chr12:6364974 | A | T | 33 | a0001c0001t0001g0175 a0001c0001t0001g0199 a0001c0001t0001g0241 others(30): Show |
35 | HG00323.hp2 HG01175.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.417-1264T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6364974 | |||||||
| chr12:6365026 | C | CT | 24 | a0001c0001t0001g0161 a0001c0001t0001g0189 a0001c0001t0001g0364 others(21): Show |
27 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.417-1317dupA | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365026 | |||||||
| chr12:6365026 | C | CTT | 102 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(99): Show |
111 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.417-1318_417-1317d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365026 | |||||||
| chr12:6365026 | C | CTTT | 8 | a0001c0001t0002g0044 a0001c0001t0002g0091 a0001c0006t0001g0113 others(5): Show |
8 | HG02055.hp1 HG02165.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.417-1319_417-1317d others(5): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365026 | |||||||
| chr12:6365093 | G | T | 3 | a0001c0001t0001g0341 a0001c0001t0005g0012 a0001c0001t0005g0138 |
4 | HG02723.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.417-1383C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365093 | |||||||
| chr12:6365118 | C | T | 10 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.417-1408G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365118 | |||||||
| chr12:6365136 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.417-1426G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365136 | |||||||
| chr12:6365171 | C | T | 1 | a0003c0003t0002g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.417-1461G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365171 | |||||||
| chr12:6365272 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.417-1562G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365272 | |||||||
| chr12:6365363 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(117): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.417-1653G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365363 | |||||||
| chr12:6365402 | T | C | 2 | a0001c0001t0004g0406 a0006c0005t0003g0156 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.417-1692A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365402 | |||||||
| chr12:6365489 | T | A | 31 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(28): Show |
32 | HG00597.hp1 HG00621.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.417-1779A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365489 | |||||||
| chr12:6365490 | C | A | 31 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(28): Show |
32 | HG00597.hp1 HG00621.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.417-1780G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365490 | |||||||
| chr12:6365650 | G | GA | 6 | a0001c0001t0001g0229 a0003c0003t0001g0232 a0003c0003t0001g0233 others(3): Show |
6 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.417-1941dupT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365650 | |||||||
| chr12:6365718 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.417-2008G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365718 | |||||||
| chr12:6365864 | C | A | 31 | a0001c0001t0001g0028 a0001c0001t0001g0155 a0001c0001t0001g0180 others(28): Show |
32 | HG00597.hp1 HG00621.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.417-2154G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365864 | |||||||
| chr12:6365886 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.417-2176C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365886 | |||||||
| chr12:6365916 | T | G | 109 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(106): Show |
118 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.417-2206A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365916 | |||||||
| chr12:6365987 | TG | T | 76 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0160 others(73): Show |
84 | HG00544.hp2 HG00673.hp1 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.417-2278delC | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6365987 | |||||||
| chr12:6366001 | C | T | 1 | a0002c0002t0001g0293 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.417-2291G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366001 | |||||||
| chr12:6366016 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.417-2306C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366016 | |||||||
| chr12:6366234 | C | T | 17 | a0001c0001t0001g0028 a0001c0001t0001g0180 a0001c0001t0001g0181 others(14): Show |
18 | HG00597.hp1 HG00621.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-2524G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366234 | |||||||
| chr12:6366499 | A | G | 1 | a0001c0001t0001g0374 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.417-2789T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366499 | |||||||
| chr12:6366710 | G | A | 1 | a0002c0002t0004g0403 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.417-3000C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366710 | |||||||
| chr12:6366724 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.417-3014G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366724 | |||||||
| chr12:6366731 | C | T | 109 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(106): Show |
118 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.417-3021G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366731 | |||||||
| chr12:6366764 | C | G | 5 | a0001c0001t0001g0210 a0002c0002t0001g0209 a0002c0002t0001g0249 others(2): Show |
5 | HG02027.hp1 HG02056.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.417-3054G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366764 | |||||||
| chr12:6366787 | C | T | 2 | a0001c0001t0004g0406 a0006c0005t0003g0156 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.417-3077G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366787 | |||||||
| chr12:6366841 | T | C | 1 | a0004c0014t0003g0108 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.417-3131A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366841 | |||||||
| chr12:6366957 | T | C | 312 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(309): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.417-3247A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6366957 | |||||||
| chr12:6367058 | C | T | 19 | a0001c0001t0001g0175 a0001c0001t0001g0241 a0001c0001t0001g0387 others(16): Show |
19 | HG00323.hp2 HG01175.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3348G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367058 | |||||||
| chr12:6367086 | A | C | 110 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(107): Show |
119 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.417-3376T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367086 | |||||||
| chr12:6367108 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.417-3398G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367108 | |||||||
| chr12:6367192 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0146 |
2 | NA18959.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.417-3482G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367192 | |||||||
| chr12:6367302 | C | T | 1 | a0001c0004t0004g0404 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.417-3592G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367302 | |||||||
| chr12:6367417 | C | T | 109 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0153 others(106): Show |
118 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.417-3707G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367417 | |||||||
| chr12:6367425 | G | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(162): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.417-3715C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367425 | |||||||
| chr12:6367557 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(164): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.417-3847G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367557 | |||||||
| chr12:6367726 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(165): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.417-4016T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367726 | |||||||
| chr12:6367833 | C | T | 1 | a0004c0009t0003g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.417-4123G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6367833 | |||||||
| chr12:6368078 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(159): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.417-4368G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368078 | |||||||
| chr12:6368165 | A | G | 1 | a0013c0023t0003g0359 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.417-4455T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368165 | |||||||
| chr12:6368197 | G | A | 2 | a0001c0001t0001g0384 a0001c0001t0002g0075 |
2 | HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.417-4487C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368197 | |||||||
| chr12:6368212 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(153): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.417-4502G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368212 | |||||||
| chr12:6368235 | C | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(302): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.417-4525G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368235 | |||||||
| chr12:6368249 | G | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0218 a0001c0001t0001g0219 others(12): Show |
17 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.417-4539C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368249 | |||||||
| chr12:6368273 | C | T | 2 | a0001c0001t0001g0373 a0002c0002t0010g0095 |
2 | NA18963.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.417-4563G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368273 | |||||||
| chr12:6368298 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(132): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.417-4588G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368298 | |||||||
| chr12:6368330 | C | T | 1 | a0002c0002t0001g0292 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.417-4620G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368330 | |||||||
| chr12:6368345 | C | G | 1 | a0008c0015t0017g0368 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.417-4635G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368345 | |||||||
| chr12:6368460 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.417-4750G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368460 | |||||||
| chr12:6368647 | G | A | 9 | a0001c0001t0001g0398 a0001c0001t0001g0402 a0001c0001t0002g0009 others(6): Show |
10 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.417-4937C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368647 | |||||||
| chr12:6368736 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.417-5026C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368736 | |||||||
| chr12:6368853 | T | C | 15 | a0001c0001t0001g0199 a0001c0001t0001g0239 a0001c0001t0001g0241 others(12): Show |
15 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.417-5143A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6368853 | |||||||
| chr12:6369203 | C | T | 1 | a0002c0002t0002g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.416+5165G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369203 | |||||||
| chr12:6369258 | G | GCTGCCAC others(16): Show |
3 | a0003c0003t0001g0168 a0003c0003t0001g0245 a0006c0026t0003g0109 |
3 | HG02055.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.416+5087_416+5109d others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369258 | |||||||
| chr12:6369258 | G | GCTGCCAC others(131): Show |
1 | a0003c0003t0001g0029 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.416+5109_416+5110i others(140): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369258 | |||||||
| chr12:6369258 | GCTGCCAC others(16): Show |
G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.416+5087_416+5109d others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369258 | |||||||
| chr12:6369273 | G | GCCTCCCT others(154): Show |
1 | a0001c0001t0004g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.416+5094_416+5095i others(163): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369273 | |||||||
| chr12:6369273 | G | GCCTCCCT others(131): Show |
1 | a0001c0001t0001g0287 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.416+5094_416+5095i others(140): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369273 | |||||||
| chr12:6369273 | GCCTCCCT others(16): Show |
G | 7 | a0001c0001t0001g0221 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
9 | HG00423.hp1 HG00438.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.416+5072_416+5094d others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369273 | |||||||
| chr12:6369292 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0004g0407 a0010c0017t0001g0344 |
3 | HG02572.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.416+5076T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369292 | |||||||
| chr12:6369294 | T | G | 3 | a0001c0001t0001g0132 a0001c0004t0001g0323 a0003c0003t0001g0339 |
3 | HG02717.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.416+5074A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(16): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0172 others(21): Show |
26 | HG00323.hp2 HG00408.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.416+5051_416+5073d others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(39): Show |
11 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0320 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.416+5028_416+5073d others(48): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(85): Show |
1 | a0004c0009t0003g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416+5073_416+5074i others(94): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(108): Show |
1 | a0003c0003t0001g0103 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.416+5073_416+5074i others(117): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(384): Show |
1 | a0001c0001t0002g0060 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.416+5073_416+5074i others(393): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(315): Show |
2 | a0007c0008t0002g0008 a0007c0008t0002g0080 |
3 | HG01256.hp1 HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.416+5073_416+5074i others(324): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | T | TCACCTCC others(338): Show |
1 | a0001c0001t0002g0092 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.416+5073_416+5074i others(347): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | TCACCTCC others(16): Show |
T | 12 | a0001c0001t0001g0290 a0001c0001t0001g0377 a0001c0001t0002g0001 others(9): Show |
12 | HG00673.hp2 HG00738.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.416+5051_416+5073d others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369294 | TCACCTCC others(39): Show |
T | 2 | a0003c0003t0002g0041 a0003c0003t0006g0230 |
2 | HG01192.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.416+5028_416+5073d others(48): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369294 | |||||||
| chr12:6369298 | C | T | 1 | a0003c0003t0001g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.416+5070G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369298 | |||||||
| chr12:6369311 | C | T | 1 | a0012c0021t0001g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.416+5057G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369311 | |||||||
| chr12:6369317 | G | T | 2 | a0001c0001t0001g0367 a0003c0003t0001g0029 |
3 | HG02896.hp2 HG02897.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.416+5051C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369317 | |||||||
| chr12:6369319 | A | ACCTCCCT others(39): Show |
1 | a0001c0001t0002g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.416+5003_416+5048d others(48): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369319 | |||||||
| chr12:6369319 | A | ACCTCCCT others(16): Show |
1 | a0003c0003t0001g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.416+5048_416+5049i others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369319 | |||||||
| chr12:6369319 | ACCTCCCT others(39): Show |
A | 8 | a0001c0001t0001g0332 a0001c0001t0001g0337 a0002c0002t0001g0330 others(5): Show |
8 | NA18945.hp1 NA18970.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.416+5003_416+5048d others(48): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369319 | |||||||
| chr12:6369321 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.416+5047G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369321 | |||||||
| chr12:6369342 | ACCTCCCT others(16): Show |
A | 57 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(54): Show |
66 | HG00544.hp2 HG00735.hp2 HG01081.hp2 others(63): Show |
intron_variant | MODIFIER | c.416+5003_416+5025d others(25): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369342 | |||||||
| chr12:6369344 | C | T | 1 | a0003c0003t0001g0245 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.416+5024G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369344 | |||||||
| chr12:6369365 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(85): Show |
98 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.416+5003C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369365 | |||||||
| chr12:6369365 | G | GCCTCCCT others(154): Show |
5 | a0001c0004t0001g0016 a0001c0004t0001g0207 a0001c0004t0001g0409 others(2): Show |
5 | HG02886.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.416+5002_416+5003i others(163): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369365 | |||||||
| chr12:6369365 | G | GCCTCCCT others(223): Show |
2 | a0001c0004t0001g0016 a0001c0004t0001g0208 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.416+5002_416+5003i others(232): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369365 | |||||||
| chr12:6369369 | C | A | 1 | a0002c0002t0007g0288 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.416+4999G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369369 | |||||||
| chr12:6369399 | C | G | 1 | a0002c0002t0002g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.416+4969G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369399 | |||||||
| chr12:6369421 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0013g0291 |
2 | NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.416+4947G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369421 | |||||||
| chr12:6369445 | A | G | 9 | a0001c0001t0001g0133 a0001c0004t0001g0016 a0001c0004t0001g0207 others(6): Show |
11 | HG02615.hp1 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.416+4923T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369445 | |||||||
| chr12:6369446 | A | C | 33 | a0001c0001t0001g0025 a0001c0001t0001g0133 a0001c0001t0001g0211 others(30): Show |
36 | HG01192.hp2 HG01261.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.416+4922T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369446 | |||||||
| chr12:6369563 | T | G | 1 | a0001c0001t0001g0361 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.416+4805A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369563 | |||||||
| chr12:6369575 | A | G | 1 | a0013c0023t0003g0359 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.416+4793T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369575 | |||||||
| chr12:6369663 | T | C | 1 | a0003c0003t0001g0386 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.416+4705A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369663 | |||||||
| chr12:6369695 | A | G | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.416+4673T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369695 | |||||||
| chr12:6369696 | T | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.416+4672A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369696 | |||||||
| chr12:6369702 | T | C | 3 | a0001c0001t0001g0289 a0001c0001t0002g0088 a0001c0001t0002g0089 |
3 | HG01070.hp1 HG01071.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.416+4666A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369702 | |||||||
| chr12:6369833 | C | CA | 17 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0226 others(14): Show |
17 | HG00639.hp2 HG00735.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.416+4534dupT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369833 | |||||||
| chr12:6369833 | C | CAA | 86 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(83): Show |
97 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.416+4533_416+4534d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369833 | |||||||
| chr12:6369833 | C | CAAA | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(32): Show |
45 | HG00408.hp2 HG00544.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.416+4532_416+4534d others(5): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369833 | |||||||
| chr12:6369833 | C | CAAAA | 10 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0313 others(7): Show |
10 | HG02004.hp2 HG02027.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.416+4531_416+4534d others(6): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369833 | |||||||
| chr12:6369833 | CA | C | 105 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0026 others(102): Show |
112 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.416+4534delT | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369833 | |||||||
| chr12:6369833 | CAA | C | 37 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(34): Show |
39 | HG02132.hp1 HG02132.hp2 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.416+4533_416+4534d others(4): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369833 | |||||||
| chr12:6369855 | A | T | 1 | a0003c0003t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416+4513T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369855 | |||||||
| chr12:6369945 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.416+4423T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6369945 | |||||||
| chr12:6370057 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
9 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.416+4311A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370057 | |||||||
| chr12:6370081 | A | G | 3 | a0003c0003t0001g0135 a0004c0009t0003g0134 a0006c0005t0003g0136 |
3 | HG02622.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.416+4287T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370081 | |||||||
| chr12:6370126 | A | C | 81 | a0001c0001t0001g0226 a0001c0001t0001g0390 a0001c0001t0001g0392 others(78): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.416+4242T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370126 | |||||||
| chr12:6370143 | C | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0352 a0001c0001t0001g0354 others(4): Show |
8 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.416+4225G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370143 | |||||||
| chr12:6370636 | C | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0325 a0001c0001t0001g0326 others(2): Show |
6 | NA18975.hp1 NA18977.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.416+3732G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370636 | |||||||
| chr12:6370644 | G | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0363 a0001c0001t0001g0364 others(26): Show |
33 | HG00673.hp1 HG01074.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.416+3724C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370644 | |||||||
| chr12:6370694 | G | A | 38 | a0001c0001t0001g0133 a0001c0001t0001g0211 a0001c0001t0001g0224 others(35): Show |
40 | HG00438.hp2 HG02132.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.416+3674C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370694 | |||||||
| chr12:6370721 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.416+3647G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6370721 | |||||||
| chr12:6371027 | G | A | 1 | a0003c0003t0001g0328 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416+3341C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371027 | |||||||
| chr12:6371078 | T | A | 1 | a0001c0001t0001g0329 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.416+3290A>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371078 | |||||||
| chr12:6371117 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.416+3251G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371117 | |||||||
| chr12:6371191 | A | G | 44 | a0001c0001t0001g0133 a0001c0001t0001g0211 a0001c0001t0001g0224 others(41): Show |
46 | HG00438.hp2 HG02132.hp1 HG02132.hp2 others(43): Show |
intron_variant | MODIFIER | c.416+3177T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371191 | |||||||
| chr12:6371259 | C | A | 1 | a0001c0001t0002g0099 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.416+3109G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371259 | |||||||
| chr12:6371260 | A | T | 38 | a0001c0001t0001g0133 a0001c0001t0001g0211 a0001c0001t0001g0224 others(35): Show |
40 | HG00438.hp2 HG02132.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.416+3108T>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371260 | |||||||
| chr12:6371285 | C | T | 1 | a0003c0003t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.416+3083G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371285 | |||||||
| chr12:6371511 | A | G | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(346): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.416+2857T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371511 | |||||||
| chr12:6371512 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(231): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.416+2856A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371512 | |||||||
| chr12:6371523 | C | CG | 14 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(11): Show |
14 | HG00544.hp2 HG00597.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.416+2844dupC | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371523 | |||||||
| chr12:6371574 | C | CG | 24 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0146 others(21): Show |
24 | HG00544.hp1 HG00642.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.416+2793dupC | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371574 | |||||||
| chr12:6371574 | C | T | 1 | a0003c0003t0001g0411 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416+2794G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371574 | |||||||
| chr12:6371790 | A | G | 3 | a0001c0001t0001g0215 a0002c0002t0001g0213 a0003c0003t0001g0214 |
3 | NA18957.hp1 NA19011.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.416+2578T>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371790 | |||||||
| chr12:6371803 | T | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(269): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.416+2565A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371803 | |||||||
| chr12:6371967 | T | G | 1 | a0002c0002t0001g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.416+2401A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6371967 | |||||||
| chr12:6372004 | G | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0363 a0001c0001t0001g0364 others(26): Show |
33 | HG00673.hp1 HG01074.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.416+2364C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372004 | |||||||
| chr12:6372681 | C | T | 3 | a0001c0004t0004g0404 a0002c0002t0004g0403 a0003c0003t0004g0405 |
3 | HG02818.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.416+1687G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372681 | |||||||
| chr12:6372713 | C | A | 9 | a0001c0001t0001g0332 a0001c0001t0001g0337 a0002c0002t0001g0330 others(6): Show |
9 | NA18945.hp1 NA18970.hp2 NA18994.hp2 others(6): Show |
intron_variant | MODIFIER | c.416+1655G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372713 | |||||||
| chr12:6372728 | T | TTCACCCT others(3): Show |
2 | a0001c0001t0001g0211 a0003c0003t0001g0212 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.416+1639_416+1640i others(12): Show |
SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372728 | |||||||
| chr12:6372729 | A | C | 2 | a0001c0001t0001g0211 a0003c0003t0001g0212 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.416+1639T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372729 | |||||||
| chr12:6372730 | A | C | 2 | a0001c0001t0001g0211 a0003c0003t0001g0212 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.416+1638T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372730 | |||||||
| chr12:6372732 | G | A | 2 | a0001c0001t0001g0211 a0003c0003t0001g0212 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.416+1636C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372732 | |||||||
| chr12:6372758 | G | T | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.416+1610C>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372758 | |||||||
| chr12:6372800 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(233): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.416+1568A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372800 | |||||||
| chr12:6372809 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.416+1559C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372809 | |||||||
| chr12:6372810 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(265): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.416+1558G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372810 | |||||||
| chr12:6372879 | A | C | 2 | a0001c0001t0001g0210 a0002c0002t0001g0209 |
2 | HG02056.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.416+1489T>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372879 | |||||||
| chr12:6372948 | C | G | 9 | a0001c0001t0001g0132 a0001c0004t0001g0016 a0001c0004t0001g0207 others(6): Show |
11 | HG02615.hp1 HG02717.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.416+1420G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6372948 | |||||||
| chr12:6373348 | T | G | 29 | a0001c0001t0001g0026 a0001c0001t0001g0363 a0001c0001t0001g0364 others(26): Show |
33 | HG00673.hp1 HG01074.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.416+1020A>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6373348 | |||||||
| chr12:6373620 | G | A | 82 | a0001c0001t0001g0390 a0001c0001t0001g0392 a0001c0001t0001g0397 others(79): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.416+748C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6373620 | |||||||
| chr12:6373692 | G | C | 2 | a0002c0002t0001g0399 a0002c0002t0001g0400 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.416+676C>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6373692 | |||||||
| chr12:6373752 | G | A | 1 | a0001c0001t0001g0401 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.416+616C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6373752 | |||||||
| chr12:6373940 | C | T | 1 | a0003c0003t0002g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.416+428G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6373940 | |||||||
| chr12:6374297 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(330): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.416+71A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6374297 | |||||||
| chr12:6374365 | G | A | 1 | a0001c0001t0001g0402 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.416+3C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 2/12 | chr12 | 6374365 | |||||||
| chr12:6374898 | G | A | 1 | a0001c0001t0001g0028 | 2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-54-61C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6374898 | |||||||
| chr12:6374907 | G | A | 2 | a0001c0004t0001g0409 a0001c0004t0001g0410 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-54-70C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6374907 | |||||||
| chr12:6374975 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-54-138G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6374975 | |||||||
| chr12:6375053 | C | T | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0015g0137 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-216G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6375053 | |||||||
| chr12:6375164 | T | C | 4 | a0001c0004t0001g0409 a0001c0004t0001g0410 a0003c0003t0001g0029 others(1): Show |
5 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54-327A>G | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6375164 | |||||||
| chr12:6375257 | G | A | 1 | a0001c0001t0011g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-55+248C>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6375257 | |||||||
| chr12:6375299 | C | A | 1 | a0003c0003t0001g0411 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-55+206G>T | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6375299 | |||||||
| chr12:6375299 | C | T | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0015g0137 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-55+206G>A | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6375299 | |||||||
| chr12:6375500 | C | G | 37 | a0001c0001t0002g0030 a0001c0001t0002g0032 a0001c0006t0001g0106 others(34): Show |
39 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.-55+5G>C | SCNN1A | ENSG00000111319.13 | transcript | ENST00000228916.7 | protein_coding | 1/12 | chr12 | 6375500 |