Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6340 |
| ensemblid | ENSG00000166828.3 |
| hgncid | 10602 |
| symbol | SCNN1G |
| name | sodium channel epithelial 1 subunit gamma |
| refseq_nuc | NM_001039.4 |
| refseq_prot | NP_001030.2 |
| ensembl_nuc | ENST00000300061.3 |
| ensembl_prot | ENSP00000300061.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 23182745 |
| end | 23216883 |
| strand | + |
| ver | v1.2 |
| region | chr16:23182745-23216883 |
| region5000 | chr16:23177745-23221883 |
| regionname0 | SCNN1G_chr16_23182745_23216883 |
| regionname5000 | SCNN1G_chr16_23177745_23221883 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 649 | 311 | 86 | 70 | 97 | 14 | 42 | 62 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| a0002 | 0/0 | 649 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| a0003 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| a0004 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| a0005 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| a0006 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| a0007 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | MAPGE others(644): Show |
chr16 | 23177745 | 23221883 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1947 | 186 | 56 | 34 | 60 | 4 | 31 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0002 | 0/0 | 1947 | 60 | 4 | 20 | 27 | 2 | 7 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0003 | 0/1 | 1947 | 44 | 17 | 10 | 8 | 4 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0004 | 0/0 | 1947 | 6 | 1 | 2 | 1 | 2 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0005 | 0/0 | 1947 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0007 | 0/0 | 1947 | 3 | 0 | 2 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0008 | 0/0 | 1947 | 2 | 0 | 1 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0009 | 0/0 | 1947 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0012 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0015 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0001c0017 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0002c0006 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0002c0010 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0003c0016 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0004c0018 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0005c0014 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0006c0013 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 | ||
| a0007c0011 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | ATGGC others(1942): Show |
chr16 | 23177745 | 23221883 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3477 | 151 | 34 | 31 | 58 | 4 | 23 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0001t0005 | 0/0 | 3477 | 13 | 4 | 3 | 2 | 0 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0001t0006 | 0/0 | 3477 | 12 | 12 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0001t0008 | 0/0 | 3477 | 5 | 5 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0001t0009 | 0/0 | 3477 | 3 | 0 | 0 | 0 | 0 | 3 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0001t0012 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0001t0013 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0002t0001 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0002t0003 | 0/0 | 3477 | 34 | 0 | 15 | 12 | 1 | 6 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0002t0004 | 0/0 | 3477 | 22 | 3 | 4 | 13 | 1 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0002t0014 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0002t0015 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0002t0016 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0003t0002 | 0/1 | 3477 | 43 | 17 | 10 | 7 | 4 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0003t0010 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0004t0001 | 0/0 | 3477 | 2 | 0 | 0 | 0 | 2 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0004t0005 | 0/0 | 3477 | 3 | 1 | 1 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0004t0011 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0005t0007 | 0/0 | 3477 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0007t0001 | 0/0 | 3477 | 3 | 0 | 2 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0008t0001 | 0/0 | 3477 | 2 | 0 | 1 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0009t0005 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0009t0017 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0012t0008 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0015t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0001c0017t0002 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0002c0006t0007 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0002c0010t0003 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0003c0016t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0004c0018t0001 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0005c0014t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0006c0013t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| a0007c0011t0005 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | GATGC others(3472): Show |
chr16 | 23177745 | 23221883 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0012g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0014g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0015g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0016g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0011g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0008t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0008t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0009t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0009t0017g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0012t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0015t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0017t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0006t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0006t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0006t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0010t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0003c0016t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0004c0018t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0005c0014t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0006c0013t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0007c0011t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0008 | t0001 | g0033 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0054 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00140 | hp2 | a0001 | c0007 | t0001 | g0056 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0267 | EUR | FIN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0292 | EUR | FIN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0289 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00423 | hp2 | a0003 | c0016 | t0001 | g0080 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0291 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0160 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0095 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0096 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0102 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0137 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0278 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01081 | hp2 | a0001 | c0004 | t0011 | g0051 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0295 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0106 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01106 | hp1 | a0001 | c0007 | t0001 | g0052 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0296 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01167 | hp2 | a0001 | c0005 | t0007 | g0251 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0168 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0281 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0053 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0258 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0255 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0283 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0187 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0261 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0185 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0183 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0055 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0223 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01891 | hp2 | a0001 | c0005 | t0007 | g0253 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0241 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0186 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0260 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0272 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02055 | hp2 | a0001 | c0005 | t0007 | g0252 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0297 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02083 | hp1 | a0001 | c0015 | t0001 | g0073 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02145 | hp2 | a0001 | c0012 | t0008 | g0179 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02165 | hp2 | a0001 | c0002 | t0015 | g0282 | EAS | CDX | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0139 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0154 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0269 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0259 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0257 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0279 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0256 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0219 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0243 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0271 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02622 | hp1 | a0002 | c0006 | t0007 | g0031 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0293 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0299 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0097 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0240 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02896 | hp1 | a0002 | c0010 | t0003 | g0032 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0184 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0094 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0196 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0157 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0249 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03130 | hp1 | a0001 | c0005 | t0007 | g0250 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0191 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0140 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03225 | hp1 | a0001 | c0009 | t0017 | g0221 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0118 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0007 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0050 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0238 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0200 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0039 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0300 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03579 | hp2 | a0001 | c0002 | t0014 | g0273 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0204 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0245 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0290 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0246 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03942 | hp2 | a0001 | c0001 | t0009 | g0239 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0228 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0287 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0285 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0003 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0171 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0242 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18939 | hp1 | a0001 | c0004 | t0005 | g0057 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18941 | hp1 | a0001 | c0003 | t0010 | g0049 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0288 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0162 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0276 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0274 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18967 | hp1 | a0005 | c0014 | t0001 | g0076 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18971 | hp2 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0264 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18998 | hp2 | a0001 | c0002 | t0004 | g0270 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19001 | hp1 | a0001 | c0002 | t0004 | g0263 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0254 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0262 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0038 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0101 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0280 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0286 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19081 | hp1 | a0001 | c0002 | t0016 | g0277 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19091 | hp1 | a0006 | c0013 | t0001 | g0180 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0268 | AFR | ASW | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0142 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0141 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01123 | hp1 | a0001 | c0008 | t0001 | g0018 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01123 | hp2 | a0001 | c0004 | t0005 | g0017 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0192 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02486 | hp1 | a0002 | c0006 | t0007 | g0029 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02486 | hp2 | a0004 | c0018 | t0001 | g0226 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02559 | hp1 | a0002 | c0006 | t0007 | g0030 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20300 | hp1 | a0007 | c0011 | t0005 | g0058 | AFR | USA | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA21309 | hp1 | a0001 | c0017 | t0002 | g0222 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA21309 | hp2 | a0001 | c0009 | t0005 | g0046 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0138 | REF | REF | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0143 | REF | REF | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23189454 | C | T | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.401C>T | p.Ser134Phe | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/13 | 514/3477 | 401/1950 | 134/649 | chr16 | 23189454 | |||
| chr16:23189600 | G | A | 1 | a0002 | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
missense_variant | MODERATE | c.547G>A | p.Gly183Ser | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/13 | 660/3477 | 547/1950 | 183/649 | chr16 | 23189600 | |||
| chr16:23192370 | G | A | 1 | a0007 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.637G>A | p.Asp213Asn | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/13 | 750/3477 | 637/1950 | 213/649 | chr16 | 23192370 | |||
| chr16:23194188 | A | G | 1 | a0003 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.827A>G | p.His276Arg | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/13 | 940/3477 | 827/1950 | 276/649 | chr16 | 23194188 | |||
| chr16:23214735 | T | C | 1 | a0006 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.1517T>C | p.Ile506Thr | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 12/13 | 1630/3477 | 1517/1950 | 506/649 | chr16 | 23214735 | |||
| chr16:23215276 | G | A | 1 | a0005 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1757G>A | p.Arg586His | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 1870/3477 | 1757/1950 | 586/649 | chr16 | 23215276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23189440 | T | C | 8 | a0001c0002 a0001c0004 a0001c0005 others(5): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
synonymous_variant | LOW | c.387T>C | p.Tyr129Tyr | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/13 | 500/3477 | 387/1950 | 129/649 | chr16 | 23189440 | |||
| chr16:23189488 | C | T | 1 | a0001c0008 | 2 | HG00099.hp1 HG01123.hp1 |
synonymous_variant | LOW | c.435C>T | p.Ser145Ser | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/13 | 548/3477 | 435/1950 | 145/649 | chr16 | 23189488 | |||
| chr16:23189527 | T | C | 8 | a0001c0002 a0001c0004 a0001c0005 others(5): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
synonymous_variant | LOW | c.474T>C | p.Ile158Ile | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/13 | 587/3477 | 474/1950 | 158/649 | chr16 | 23189527 | |||
| chr16:23189602 | C | T | 5 | a0001c0004 a0001c0007 a0001c0009 others(2): Show |
13 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(10): Show |
synonymous_variant | LOW | c.549C>T | p.Gly183Gly | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/13 | 662/3477 | 549/1950 | 183/649 | chr16 | 23189602 | |||
| chr16:23192369 | C | T | 1 | a0001c0007 | 3 | HG00140.hp2 HG01106.hp1 HG01256.hp2 |
synonymous_variant | LOW | c.636C>T | p.Ser212Ser | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/13 | 749/3477 | 636/1950 | 212/649 | chr16 | 23192369 | |||
| chr16:23197304 | C | T | 1 | a0001c0015 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.954C>T | p.Asn318Asn | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/13 | 1067/3477 | 954/1950 | 318/649 | chr16 | 23197304 | |||
| chr16:23213122 | C | A | 1 | a0001c0012 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1452C>A | p.Leu484Leu | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/13 | 1565/3477 | 1452/1950 | 484/649 | chr16 | 23213122 | |||
| chr16:23215466 | C | G | 4 | a0001c0003 a0001c0005 a0001c0017 others(1): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
synonymous_variant | LOW | c.1947C>G | p.Leu649Leu | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 2060/3477 | 1947/1950 | 649/649 | chr16 | 23215466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23182781 | C | T | 1 | a0001c0009t0017 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-77C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/13 | 3491 | chr16 | 23182781 | ||||||
| chr16:23186241 | A | G | 8 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0014 others(5): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
5_prime_UTR_variant | MODIFIER | c.-31A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/13 | 31 | chr16 | 23186241 | ||||||
| chr16:23215513 | G | T | 1 | a0001c0001t0013 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 44 | chr16 | 23215513 | ||||||
| chr16:23215544 | G | A | 1 | a0001c0002t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 75 | chr16 | 23215544 | ||||||
| chr16:23215575 | G | A | 1 | a0001c0001t0009 | 3 | HG03017.hp1 HG03688.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*106G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 106 | chr16 | 23215575 | ||||||
| chr16:23215623 | G | T | 1 | a0001c0001t0009 | 3 | HG03017.hp1 HG03688.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*154G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 154 | chr16 | 23215623 | ||||||
| chr16:23215628 | T | G | 5 | a0001c0003t0002 a0001c0003t0010 a0001c0005t0007 others(2): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*159T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 159 | chr16 | 23215628 | ||||||
| chr16:23215699 | C | T | 1 | a0001c0001t0012 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 230 | chr16 | 23215699 | ||||||
| chr16:23215705 | C | T | 5 | a0001c0003t0002 a0001c0003t0010 a0001c0005t0007 others(2): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*236C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 236 | chr16 | 23215705 | ||||||
| chr16:23215737 | G | A | 5 | a0001c0003t0002 a0001c0003t0010 a0001c0005t0007 others(2): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*268G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 268 | chr16 | 23215737 | ||||||
| chr16:23215960 | G | A | 1 | a0001c0002t0015 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 491 | chr16 | 23215960 | ||||||
| chr16:23216041 | A | G | 12 | a0001c0001t0005 a0001c0002t0003 a0001c0002t0015 others(9): Show |
106 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*572A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 572 | chr16 | 23216041 | ||||||
| chr16:23216075 | T | A | 5 | a0001c0003t0002 a0001c0003t0010 a0001c0005t0007 others(2): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*606T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 606 | chr16 | 23216075 | ||||||
| chr16:23216128 | T | C | 12 | a0001c0001t0005 a0001c0002t0003 a0001c0002t0015 others(9): Show |
106 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*659T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 659 | chr16 | 23216128 | ||||||
| chr16:23216144 | A | G | 5 | a0001c0003t0002 a0001c0003t0010 a0001c0005t0007 others(2): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*675A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 675 | chr16 | 23216144 | ||||||
| chr16:23216258 | T | C | 12 | a0001c0001t0005 a0001c0002t0003 a0001c0002t0015 others(9): Show |
106 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*789T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 789 | chr16 | 23216258 | ||||||
| chr16:23216259 | C | T | 5 | a0001c0003t0002 a0001c0003t0010 a0001c0005t0007 others(2): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*790C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 790 | chr16 | 23216259 | ||||||
| chr16:23216616 | A | G | 1 | a0001c0002t0016 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1147A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 1147 | chr16 | 23216616 | ||||||
| chr16:23216730 | G | A | 3 | a0001c0001t0008 a0001c0009t0017 a0001c0012t0008 |
7 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1261G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 1261 | chr16 | 23216730 | ||||||
| chr16:23216831 | T | C | 1 | a0001c0003t0010 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 1362 | chr16 | 23216831 | ||||||
| chr16:23216838 | C | T | 1 | a0001c0001t0006 | 12 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1369C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 1369 | chr16 | 23216838 | ||||||
| chr16:23216839 | G | A | 1 | a0001c0004t0011 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 13/13 | 1370 | chr16 | 23216839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:23182875 | G | A | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-45+62G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23182875 | |||||||
| chr16:23182918 | C | A | 1 | a0001c0008t0001g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-45+105C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23182918 | |||||||
| chr16:23182929 | C | G | 57 | a0001c0001t0013g0300 a0001c0002t0003g0001 a0001c0002t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-45+116C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23182929 | |||||||
| chr16:23183088 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
10 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-45+275T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183088 | |||||||
| chr16:23183097 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-45+284C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183097 | |||||||
| chr16:23183137 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-45+324C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183137 | |||||||
| chr16:23183312 | G | A | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+499G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183312 | |||||||
| chr16:23183628 | G | A | 2 | a0001c0008t0001g0018 a0001c0008t0001g0033 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-45+815G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183628 | |||||||
| chr16:23183664 | C | T | 4 | a0001c0001t0001g0244 a0001c0001t0005g0245 a0001c0001t0005g0246 others(1): Show |
4 | HG03704.hp1 HG03831.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+851C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183664 | |||||||
| chr16:23183686 | G | A | 3 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 |
3 | HG02486.hp1 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-45+873G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183686 | |||||||
| chr16:23183699 | CTG | C | 55 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(52): Show |
63 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-45+888_-45+889del others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23183699 | ||||||
| chr16:23183733 | A | G | 2 | a0001c0003t0002g0242 a0001c0003t0002g0243 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-45+920A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183733 | |||||||
| chr16:23183836 | G | T | 3 | a0001c0004t0005g0017 a0001c0008t0001g0018 a0001c0008t0001g0033 |
3 | HG00099.hp1 HG01123.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-45+1023G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183836 | |||||||
| chr16:23183966 | C | G | 2 | a0001c0003t0002g0240 a0001c0003t0002g0241 |
2 | HG01934.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-45+1153C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23183966 | |||||||
| chr16:23184008 | C | A | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-45+1195C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184008 | |||||||
| chr16:23184195 | TG | T | 63 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(60): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-45+1387delG | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23184195 | ||||||
| chr16:23184306 | T | A | 5 | a0001c0005t0007g0249 a0001c0005t0007g0250 a0001c0005t0007g0251 others(2): Show |
5 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+1493T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184306 | |||||||
| chr16:23184325 | T | C | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-45+1512T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184325 | |||||||
| chr16:23184396 | C | T | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-45+1583C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184396 | |||||||
| chr16:23184445 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-45+1632T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184445 | |||||||
| chr16:23184581 | A | G | 1 | a0001c0001t0009g0239 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-44-1647A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184581 | |||||||
| chr16:23184603 | T | G | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-44-1625T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184603 | |||||||
| chr16:23184672 | A | C | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-44-1556A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184672 | |||||||
| chr16:23184715 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-44-1513A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184715 | |||||||
| chr16:23184748 | G | GA | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-44-1473dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23184748 | ||||||
| chr16:23184776 | G | A | 5 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1452G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184776 | |||||||
| chr16:23184806 | A | G | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-44-1422A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184806 | |||||||
| chr16:23184822 | T | C | 63 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(60): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-44-1406T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184822 | |||||||
| chr16:23184948 | A | C | 1 | a0001c0002t0004g0298 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-44-1280A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23184948 | |||||||
| chr16:23185270 | T | C | 56 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(53): Show |
64 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-44-958T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185270 | |||||||
| chr16:23185417 | C | T | 63 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(60): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-44-811C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185417 | |||||||
| chr16:23185710 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-44-518T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185710 | |||||||
| chr16:23185713 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-44-515C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185713 | |||||||
| chr16:23185794 | A | G | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-44-434A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185794 | |||||||
| chr16:23185921 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | NA18963.hp2 NA18966.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-307G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185921 | |||||||
| chr16:23185981 | C | T | 56 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(53): Show |
64 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-44-247C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185981 | |||||||
| chr16:23185984 | A | C | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-244A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185984 | |||||||
| chr16:23185985 | CGGCTAGG others(5): Show |
C | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-240_-44-229del others(12): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23185985 | ||||||
| chr16:23185998 | G | A | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-230G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23185998 | |||||||
| chr16:23186021 | T | C | 1 | a0001c0009t0005g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-44-207T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23186021 | |||||||
| chr16:23186224 | C | G | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.-44-4C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 1/12 | chr16 | 23186224 | |||||||
| chr16:23186614 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.317+26G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186614 | |||||||
| chr16:23186733 | C | T | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+145C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186733 | |||||||
| chr16:23186852 | C | T | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+264C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186852 | |||||||
| chr16:23186868 | G | A | 60 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(57): Show |
68 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+280G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186868 | |||||||
| chr16:23186869 | T | C | 1 | a0001c0002t0004g0254 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.317+281T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186869 | |||||||
| chr16:23186923 | C | G | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+335C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186923 | |||||||
| chr16:23186924 | G | A | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.317+336G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186924 | |||||||
| chr16:23186958 | C | T | 1 | a0001c0003t0002g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.317+370C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23186958 | |||||||
| chr16:23187057 | C | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG01106.hp2 HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.317+469C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187057 | |||||||
| chr16:23187106 | C | CT | 67 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(64): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.317+537dupT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 23187106 | ||||||
| chr16:23187106 | C | CTT | 8 | a0001c0002t0003g0016 a0001c0002t0003g0292 a0001c0002t0003g0293 others(5): Show |
9 | HG00280.hp2 HG00558.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.317+536_317+537dup others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 23187106 | ||||||
| chr16:23187106 | CT | C | 7 | a0001c0003t0002g0050 a0001c0003t0010g0049 a0001c0004t0005g0017 others(4): Show |
7 | HG01123.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+537delT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 23187106 | ||||||
| chr16:23187109 | T | TC | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0002t0003g0255 |
3 | HG01261.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.317+521_317+522ins others(1): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187109 | |||||||
| chr16:23187110 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.317+522T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187110 | |||||||
| chr16:23187135 | G | T | 5 | a0001c0005t0007g0249 a0001c0005t0007g0250 a0001c0005t0007g0251 others(2): Show |
5 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+547G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187135 | |||||||
| chr16:23187143 | C | T | 55 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(52): Show |
63 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.317+555C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187143 | |||||||
| chr16:23187175 | C | T | 55 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(52): Show |
63 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.317+587C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187175 | |||||||
| chr16:23187183 | C | A | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+595C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187183 | |||||||
| chr16:23187215 | T | C | 6 | a0001c0008t0001g0018 a0001c0008t0001g0033 a0002c0006t0007g0029 others(3): Show |
6 | HG00099.hp1 HG01123.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+627T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187215 | |||||||
| chr16:23187317 | C | G | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.317+729C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187317 | |||||||
| chr16:23187446 | G | T | 3 | a0001c0009t0005g0046 a0001c0009t0017g0221 a0001c0017t0002g0222 |
3 | HG03225.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.317+858G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187446 | |||||||
| chr16:23187505 | C | G | 1 | a0001c0001t0008g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.317+917C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187505 | |||||||
| chr16:23187573 | C | A | 1 | a0001c0002t0004g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.317+985C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187573 | |||||||
| chr16:23187575 | G | A | 65 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(62): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.317+987G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187575 | |||||||
| chr16:23187710 | C | T | 1 | a0001c0008t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.317+1122C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187710 | |||||||
| chr16:23187742 | CT | C | 4 | a0001c0002t0003g0258 a0001c0002t0003g0259 a0001c0002t0003g0260 others(1): Show |
4 | HG01257.hp2 HG01496.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+1155delT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187742 | |||||||
| chr16:23187818 | G | A | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0057 others(4): Show |
7 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+1230G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187818 | |||||||
| chr16:23187923 | G | A | 13 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0057 others(10): Show |
13 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(10): Show |
intron_variant | MODIFIER | c.317+1335G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187923 | |||||||
| chr16:23187968 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.317+1380C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23187968 | |||||||
| chr16:23188083 | C | T | 1 | a0001c0002t0003g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.318-1288C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188083 | |||||||
| chr16:23188307 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | NA18998.hp1 NA19007.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-1064G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188307 | |||||||
| chr16:23188541 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.318-830A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188541 | |||||||
| chr16:23188554 | T | C | 1 | a0001c0002t0003g0262 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.318-817T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188554 | |||||||
| chr16:23188612 | G | T | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.318-759G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188612 | |||||||
| chr16:23188722 | G | A | 6 | a0001c0008t0001g0018 a0001c0008t0001g0033 a0002c0006t0007g0029 others(3): Show |
6 | HG00099.hp1 HG01123.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.318-649G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188722 | |||||||
| chr16:23188746 | C | T | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-625C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188746 | |||||||
| chr16:23188786 | A | T | 35 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(32): Show |
41 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.318-585A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188786 | |||||||
| chr16:23188856 | G | A | 2 | a0001c0002t0003g0274 a0001c0003t0002g0238 |
2 | HG03491.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.318-515G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188856 | |||||||
| chr16:23188912 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.318-459A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188912 | |||||||
| chr16:23188954 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.318-417G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23188954 | |||||||
| chr16:23189033 | C | T | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.318-338C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23189033 | |||||||
| chr16:23189132 | T | A | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-239T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23189132 | |||||||
| chr16:23189235 | G | A | 1 | a0001c0002t0003g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.318-136G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23189235 | |||||||
| chr16:23189272 | T | C | 73 | a0001c0002t0001g0063 a0001c0002t0003g0001 a0001c0002t0003g0003 others(70): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.318-99T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 2/12 | chr16 | 23189272 | |||||||
| chr16:23189726 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.618+55T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23189726 | |||||||
| chr16:23189777 | T | C | 63 | a0001c0002t0001g0063 a0001c0002t0003g0001 a0001c0002t0003g0003 others(60): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.618+106T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23189777 | |||||||
| chr16:23189870 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.618+199G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23189870 | |||||||
| chr16:23190067 | T | TA | 65 | a0001c0002t0001g0063 a0001c0002t0003g0001 a0001c0002t0003g0003 others(62): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.618+406dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190067 | ||||||
| chr16:23190134 | C | T | 6 | a0001c0008t0001g0018 a0001c0008t0001g0033 a0002c0006t0007g0029 others(3): Show |
6 | HG00099.hp1 HG01123.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.618+463C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190134 | |||||||
| chr16:23190263 | AAGAAAGA others(5): Show |
A | 1 | a0001c0001t0001g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.618+604_618+615del others(12): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190263 | ||||||
| chr16:23190559 | A | G | 1 | a0001c0017t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.618+888A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190559 | |||||||
| chr16:23190591 | G | A | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+920G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190591 | |||||||
| chr16:23190598 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
13 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.618+927C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190598 | |||||||
| chr16:23190603 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.618+932G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190603 | |||||||
| chr16:23190793 | G | T | 2 | a0002c0006t0007g0030 a0002c0006t0007g0031 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.618+1122G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190793 | |||||||
| chr16:23190795 | T | C | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+1124T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190795 | |||||||
| chr16:23190831 | A | AT | 52 | a0001c0001t0001g0034 a0001c0001t0001g0062 a0001c0001t0001g0158 others(49): Show |
52 | HG00408.hp1 HG00597.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.618+1190dupT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190831 | ||||||
| chr16:23190831 | A | ATT | 16 | a0001c0001t0001g0047 a0001c0001t0001g0195 a0001c0001t0001g0197 others(13): Show |
17 | HG01070.hp1 HG01074.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+1189_618+1190d others(4): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190831 | ||||||
| chr16:23190831 | A | ATTT | 16 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0201 others(13): Show |
17 | HG00140.hp1 HG00544.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+1188_618+1190d others(5): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190831 | ||||||
| chr16:23190831 | AT | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.618+1190delT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190831 | ||||||
| chr16:23190831 | ATT | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0068 a0001c0001t0001g0224 others(5): Show |
8 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+1189_618+1190d others(4): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190831 | ||||||
| chr16:23190831 | ATTTTTTT others(12): Show |
A | 2 | a0001c0001t0006g0067 a0001c0001t0006g0223 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.618+1172_618+1190d others(21): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23190831 | ||||||
| chr16:23190888 | C | G | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+1217C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190888 | |||||||
| chr16:23190955 | T | A | 1 | a0001c0002t0003g0283 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.618+1284T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23190955 | |||||||
| chr16:23191065 | G | A | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-1287G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191065 | |||||||
| chr16:23191073 | G | A | 1 | a0001c0003t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.619-1279G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191073 | |||||||
| chr16:23191419 | CTT | C | 9 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0057 others(6): Show |
9 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-931_619-930del others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23191419 | ||||||
| chr16:23191553 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.619-799G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191553 | |||||||
| chr16:23191625 | C | T | 35 | a0001c0002t0003g0001 a0001c0002t0003g0003 a0001c0002t0003g0016 others(32): Show |
41 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.619-727C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191625 | |||||||
| chr16:23191635 | G | A | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-717G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191635 | |||||||
| chr16:23191645 | C | T | 1 | a0001c0003t0002g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619-707C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191645 | |||||||
| chr16:23191661 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.619-691A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191661 | |||||||
| chr16:23191832 | A | G | 1 | a0007c0011t0005g0058 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.619-520A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23191832 | |||||||
| chr16:23192019 | G | A | 1 | a0001c0004t0005g0017 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.619-333G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23192019 | |||||||
| chr16:23192078 | G | GA | 73 | a0001c0002t0001g0063 a0001c0002t0003g0001 a0001c0002t0003g0003 others(70): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.619-273dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 23192078 | ||||||
| chr16:23192126 | G | A | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-226G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23192126 | |||||||
| chr16:23192274 | G | T | 2 | a0001c0008t0001g0018 a0001c0008t0001g0033 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.619-78G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23192274 | |||||||
| chr16:23192281 | A | C | 1 | a0001c0002t0004g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.619-71A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 3/12 | chr16 | 23192281 | |||||||
| chr16:23192613 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0156 |
3 | HG00735.hp2 HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.809+71C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23192613 | |||||||
| chr16:23192881 | T | C | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.809+339T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23192881 | |||||||
| chr16:23192975 | A | G | 1 | a0001c0002t0003g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.809+433A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23192975 | |||||||
| chr16:23192985 | C | T | 57 | a0001c0002t0001g0063 a0001c0002t0003g0001 a0001c0002t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.809+443C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23192985 | |||||||
| chr16:23192998 | G | A | 1 | a0001c0002t0004g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.809+456G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23192998 | |||||||
| chr16:23193001 | G | A | 4 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+459G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193001 | |||||||
| chr16:23193069 | C | CA | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
93 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.809+555dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193069 | ||||||
| chr16:23193069 | C | CAA | 41 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0041 others(38): Show |
41 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.809+554_809+555dup others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193069 | ||||||
| chr16:23193069 | C | CAAA | 8 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0104 others(5): Show |
8 | HG02080.hp1 HG02135.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.809+553_809+555dup others(3): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193069 | ||||||
| chr16:23193069 | C | CAAAAAAA others(6): Show |
1 | a0001c0009t0017g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.809+543_809+555dup others(13): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193069 | ||||||
| chr16:23193069 | CAA | C | 8 | a0001c0001t0001g0155 a0001c0004t0001g0054 a0001c0004t0001g0055 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.809+554_809+555del others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193069 | ||||||
| chr16:23193069 | CAAAAAAA others(2): Show |
C | 59 | a0001c0002t0001g0063 a0001c0002t0003g0001 a0001c0002t0003g0003 others(56): Show |
67 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.809+547_809+555del others(9): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193069 | ||||||
| chr16:23193254 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.809+712G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193254 | |||||||
| chr16:23193356 | G | A | 1 | a0002c0010t0003g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.809+814G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193356 | |||||||
| chr16:23193377 | T | C | 1 | a0001c0009t0017g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.810-794T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193377 | |||||||
| chr16:23193443 | C | T | 1 | a0001c0002t0004g0299 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.810-728C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193443 | |||||||
| chr16:23193677 | A | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.810-494A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193677 | |||||||
| chr16:23193691 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.810-480G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193691 | |||||||
| chr16:23193751 | C | T | 10 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0005g0017 others(7): Show |
10 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.810-420C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193751 | |||||||
| chr16:23193808 | G | GCCCTGGG others(101): Show |
1 | a0001c0017t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.810-345_810-344ins others(108): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193808 | ||||||
| chr16:23193966 | G | T | 3 | a0001c0009t0005g0046 a0001c0009t0017g0221 a0001c0017t0002g0222 |
3 | HG03225.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.810-205G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | chr16 | 23193966 | |||||||
| chr16:23193967 | CAG | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
180 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.810-199_810-198del others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23193967 | ||||||
| chr16:23194311 | C | T | 1 | a0001c0009t0017g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.913+37C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194311 | |||||||
| chr16:23194324 | T | C | 3 | a0001c0002t0004g0284 a0001c0004t0001g0054 a0001c0004t0005g0057 |
3 | HG00099.hp2 NA18939.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.913+50T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194324 | |||||||
| chr16:23194336 | G | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0077 others(103): Show |
114 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.913+62G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194336 | |||||||
| chr16:23194632 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.913+358G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194632 | |||||||
| chr16:23194910 | G | T | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.913+636G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194910 | |||||||
| chr16:23194946 | G | A | 2 | a0001c0004t0005g0017 a0007c0011t0005g0058 |
2 | HG01123.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.913+672G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194946 | |||||||
| chr16:23194969 | T | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.913+695T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23194969 | |||||||
| chr16:23195121 | C | T | 1 | a0001c0002t0003g0297 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.913+847C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195121 | |||||||
| chr16:23195287 | C | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
187 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.913+1013C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195287 | |||||||
| chr16:23195291 | C | T | 39 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(36): Show |
41 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.913+1017C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195291 | |||||||
| chr16:23195327 | T | G | 1 | a0001c0008t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.913+1053T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195327 | |||||||
| chr16:23195396 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
4 | HG02970.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+1122C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195396 | |||||||
| chr16:23195598 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.913+1324T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195598 | |||||||
| chr16:23195782 | G | A | 1 | a0002c0010t0003g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.914-1482G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195782 | |||||||
| chr16:23195785 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.914-1479T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195785 | |||||||
| chr16:23195787 | CA | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
187 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.914-1474delA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 23195787 | ||||||
| chr16:23196153 | G | T | 46 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(43): Show |
48 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.914-1111G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196153 | |||||||
| chr16:23196154 | G | T | 1 | a0001c0012t0008g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914-1110G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196154 | |||||||
| chr16:23196158 | G | C | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.914-1106G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196158 | |||||||
| chr16:23196261 | C | T | 2 | a0002c0006t0007g0030 a0002c0006t0007g0031 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.914-1003C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196261 | |||||||
| chr16:23196385 | A | AG | 46 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(43): Show |
48 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.914-876dupG | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 23196385 | ||||||
| chr16:23196425 | T | G | 2 | a0001c0002t0004g0015 a0001c0002t0004g0263 |
3 | HG00544.hp1 NA19001.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.914-839T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196425 | |||||||
| chr16:23196518 | C | T | 1 | a0001c0002t0015g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.914-746C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196518 | |||||||
| chr16:23196547 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.914-717T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196547 | |||||||
| chr16:23196673 | G | T | 47 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(44): Show |
49 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.914-591G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196673 | |||||||
| chr16:23196702 | G | A | 3 | a0001c0001t0012g0228 a0001c0008t0001g0018 a0001c0008t0001g0033 |
3 | HG00099.hp1 HG01123.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.914-562G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196702 | |||||||
| chr16:23196796 | T | G | 47 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(44): Show |
49 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.914-468T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196796 | |||||||
| chr16:23196811 | A | G | 47 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(44): Show |
49 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.914-453A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196811 | |||||||
| chr16:23196836 | G | A | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.914-428G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196836 | |||||||
| chr16:23197450 | A | T | 1 | a0007c0011t0005g0058 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1077+23A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23197450 | |||||||
| chr16:23197633 | C | T | 1 | a0002c0010t0003g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1077+206C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23197633 | |||||||
| chr16:23197679 | A | T | 2 | a0001c0002t0004g0256 a0001c0002t0004g0257 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1077+252A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23197679 | |||||||
| chr16:23197878 | CA | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
238 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1077+464delA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23197878 | ||||||
| chr16:23198273 | G | A | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+846G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198273 | |||||||
| chr16:23198285 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1077+858C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198285 | |||||||
| chr16:23198324 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 |
3 | HG02723.hp1 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1077+897G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198324 | |||||||
| chr16:23198423 | T | TAGAGAGA others(8): Show |
1 | a0001c0002t0015g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1077+999_1077+1000 others(18): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23198423 | ||||||
| chr16:23198511 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1077+1084A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198511 | |||||||
| chr16:23198700 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1077+1273T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198700 | |||||||
| chr16:23198817 | G | A | 1 | a0002c0010t0003g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1077+1390G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198817 | |||||||
| chr16:23198858 | C | T | 11 | a0001c0002t0004g0014 a0001c0002t0004g0015 a0001c0002t0004g0254 others(8): Show |
13 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1077+1431C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23198858 | |||||||
| chr16:23199025 | AT | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1077+1608delT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23199025 | ||||||
| chr16:23199044 | A | G | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+1617A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199044 | |||||||
| chr16:23199275 | G | A | 4 | a0001c0001t0005g0233 a0001c0001t0005g0234 a0001c0003t0002g0101 others(1): Show |
4 | HG02258.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+1848G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199275 | |||||||
| chr16:23199318 | G | T | 1 | a0001c0009t0017g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077+1891G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199318 | |||||||
| chr16:23199409 | T | C | 1 | a0001c0002t0003g0278 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1077+1982T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199409 | |||||||
| chr16:23199663 | C | CT | 19 | a0001c0001t0001g0040 a0001c0001t0001g0069 a0001c0001t0001g0117 others(16): Show |
19 | HG00140.hp1 HG00621.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1077+2262dupT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23199663 | ||||||
| chr16:23199663 | CT | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1077+2262delT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23199663 | ||||||
| chr16:23199663 | CTT | C | 51 | a0001c0001t0001g0182 a0001c0001t0001g0235 a0001c0001t0001g0236 others(48): Show |
55 | HG00544.hp1 HG00597.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.1077+2261_1077+226 others(6): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23199663 | ||||||
| chr16:23199663 | CTTT | C | 8 | a0001c0001t0005g0245 a0001c0002t0004g0264 a0001c0002t0004g0270 others(5): Show |
8 | HG01167.hp2 HG01891.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077+2260_1077+226 others(7): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23199663 | ||||||
| chr16:23199663 | CTTTTTTT | C | 9 | a0001c0001t0006g0010 a0001c0001t0006g0067 a0001c0001t0006g0124 others(6): Show |
10 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+2256_1077+226 others(11): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23199663 | ||||||
| chr16:23199761 | T | A | 4 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0001t0005g0247 others(1): Show |
4 | HG01261.hp2 HG03704.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+2334T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199761 | |||||||
| chr16:23199828 | C | T | 39 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(36): Show |
41 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1077+2401C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199828 | |||||||
| chr16:23199835 | C | T | 3 | a0001c0003t0002g0102 a0001c0003t0002g0142 a0001c0003t0002g0186 |
3 | HG00738.hp2 HG01934.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1077+2408C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199835 | |||||||
| chr16:23199853 | A | G | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1077+2426A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199853 | |||||||
| chr16:23199893 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1077+2466G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199893 | |||||||
| chr16:23199918 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1077+2491G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199918 | |||||||
| chr16:23199931 | G | A | 1 | a0001c0001t0012g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1077+2504G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199931 | |||||||
| chr16:23199966 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1077+2539T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199966 | |||||||
| chr16:23199998 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
189 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1077+2571G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23199998 | |||||||
| chr16:23200155 | A | G | 1 | a0001c0002t0003g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1077+2728A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200155 | |||||||
| chr16:23200168 | C | T | 46 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(43): Show |
53 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1077+2741C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200168 | |||||||
| chr16:23200482 | T | C | 2 | a0001c0001t0001g0070 a0003c0016t0001g0080 |
2 | HG00423.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1077+3055T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200482 | |||||||
| chr16:23200526 | C | T | 1 | a0001c0002t0004g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1077+3099C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200526 | |||||||
| chr16:23200587 | G | A | 46 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(43): Show |
53 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1077+3160G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200587 | |||||||
| chr16:23200639 | C | G | 47 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(44): Show |
54 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1077+3212C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200639 | |||||||
| chr16:23200698 | C | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1077+3271C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200698 | |||||||
| chr16:23200868 | C | G | 47 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(44): Show |
54 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1077+3441C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200868 | |||||||
| chr16:23200897 | T | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0144 others(18): Show |
24 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1077+3470T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200897 | |||||||
| chr16:23201073 | A | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0177 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+3646A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201073 | |||||||
| chr16:23201105 | T | C | 1 | a0001c0017t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1077+3678T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201105 | |||||||
| chr16:23201441 | C | A | 2 | a0001c0001t0009g0196 a0001c0001t0009g0204 |
2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1077+4014C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201441 | |||||||
| chr16:23201456 | G | A | 1 | a0001c0003t0002g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1077+4029G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201456 | |||||||
| chr16:23201458 | T | G | 1 | a0001c0001t0005g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1077+4031T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201458 | |||||||
| chr16:23201512 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1077+4085A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201512 | |||||||
| chr16:23201529 | C | CA | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
104 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1077+4113dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23201529 | ||||||
| chr16:23201531 | A | AC | 76 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0047 others(73): Show |
84 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1077+4104_1077+410 others(5): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201531 | |||||||
| chr16:23201532 | A | C | 4 | a0001c0003t0002g0142 a0001c0003t0002g0186 a0001c0007t0001g0052 others(1): Show |
4 | HG01106.hp1 HG01123.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+4105A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201532 | |||||||
| chr16:23201724 | T | C | 1 | a0001c0002t0003g0279 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1077+4297T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23201724 | |||||||
| chr16:23202077 | A | G | 1 | a0001c0003t0002g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1077+4650A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202077 | |||||||
| chr16:23202087 | G | A | 7 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 others(4): Show |
7 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+4660G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202087 | |||||||
| chr16:23202146 | A | G | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+4719A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202146 | |||||||
| chr16:23202248 | A | ATGGG | 6 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0064 others(3): Show |
6 | HG00738.hp1 HG01081.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+4837_1077+484 others(8): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23202248 | ||||||
| chr16:23202264 | G | GTGGA | 26 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0001g0146 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.1077+4883_1077+488 others(8): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23202264 | ||||||
| chr16:23202264 | GTGGA | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(43): Show |
48 | HG00140.hp1 HG00673.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1077+4883_1077+488 others(8): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23202264 | ||||||
| chr16:23202264 | GTGGATGG others(1): Show |
G | 3 | a0001c0001t0001g0042 a0001c0003t0002g0141 a0002c0010t0003g0032 |
3 | HG02896.hp1 NA18963.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1077+4879_1077+488 others(12): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23202264 | ||||||
| chr16:23202276 | A | G | 1 | a0001c0003t0002g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1077+4849A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202276 | |||||||
| chr16:23202342 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077+4915G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202342 | |||||||
| chr16:23202344 | A | C | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+4917A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202344 | |||||||
| chr16:23202559 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1077+5132A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202559 | |||||||
| chr16:23202744 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1077+5317A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202744 | |||||||
| chr16:23202903 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1077+5476G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23202903 | |||||||
| chr16:23203022 | C | A | 3 | a0001c0001t0012g0228 a0001c0008t0001g0018 a0001c0008t0001g0033 |
3 | HG00099.hp1 HG01123.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1077+5595C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203022 | |||||||
| chr16:23203060 | A | G | 1 | a0001c0004t0005g0057 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1077+5633A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203060 | |||||||
| chr16:23203078 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1077+5651A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203078 | |||||||
| chr16:23203294 | G | A | 2 | a0001c0004t0001g0055 a0001c0004t0011g0051 |
2 | HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1077+5867G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203294 | |||||||
| chr16:23203327 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1077+5900G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203327 | |||||||
| chr16:23203597 | T | C | 1 | a0001c0002t0003g0294 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1078-6153T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203597 | |||||||
| chr16:23203634 | G | A | 48 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(45): Show |
50 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1078-6116G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203634 | |||||||
| chr16:23203637 | G | C | 1 | a0001c0001t0013g0300 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1078-6113G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203637 | |||||||
| chr16:23203711 | G | A | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1078-6039G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203711 | |||||||
| chr16:23203765 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0108 |
2 | NA18969.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1078-5985G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203765 | |||||||
| chr16:23203769 | C | CA | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(170): Show |
185 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1078-5954dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23203769 | ||||||
| chr16:23203769 | C | CAA | 42 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0044 others(39): Show |
43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.1078-5955_1078-595 others(6): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23203769 | ||||||
| chr16:23203769 | C | CAAA | 6 | a0001c0001t0001g0104 a0001c0001t0001g0244 a0001c0004t0005g0219 others(3): Show |
6 | HG01891.hp2 HG02135.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-5956_1078-595 others(7): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23203769 | ||||||
| chr16:23203769 | CAA | C | 9 | a0001c0002t0004g0014 a0001c0002t0004g0015 a0001c0002t0004g0254 others(6): Show |
11 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078-5955_1078-595 others(6): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23203769 | ||||||
| chr16:23203818 | A | C | 1 | a0001c0002t0003g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078-5932A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23203818 | |||||||
| chr16:23204048 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1078-5702C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204048 | |||||||
| chr16:23204288 | C | CATATATA others(3): Show |
2 | a0001c0002t0003g0295 a0001c0002t0014g0273 |
2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1078-5424_1078-541 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0042 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1078-5426_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CAT | C | 24 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0086 others(21): Show |
24 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1078-5416_1078-541 others(6): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATAT | C | 30 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0075 others(27): Show |
31 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1078-5418_1078-541 others(8): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATAT | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0071 others(30): Show |
34 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1078-5420_1078-541 others(10): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(1): Show |
C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(26): Show |
32 | HG00597.hp1 HG00733.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1078-5422_1078-541 others(12): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(3): Show |
C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0126 a0001c0001t0001g0207 others(6): Show |
10 | HG00099.hp2 HG01070.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-5424_1078-541 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(5): Show |
C | 12 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0066 others(9): Show |
12 | HG00280.hp1 HG01106.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1078-5426_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(7): Show |
C | 7 | a0001c0001t0001g0098 a0001c0001t0001g0159 a0001c0001t0008g0036 others(4): Show |
7 | HG01099.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-5428_1078-541 others(18): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(9): Show |
C | 2 | a0001c0004t0005g0017 a0001c0004t0005g0219 |
2 | HG01123.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1078-5430_1078-541 others(20): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(11): Show |
C | 1 | a0001c0002t0003g0297 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1078-5432_1078-541 others(22): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(13): Show |
C | 1 | a0001c0004t0005g0057 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1078-5434_1078-541 others(24): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(17): Show |
C | 2 | a0001c0001t0001g0060 a0001c0002t0015g0282 |
2 | HG02165.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1078-5438_1078-541 others(28): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204288 | CATATATA others(19): Show |
C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02027.hp1 NA18998.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-5440_1078-541 others(30): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204288 | ||||||
| chr16:23204290 | T | TATATATA others(41): Show |
1 | a0001c0002t0003g0262 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1078-5419_1078-541 others(52): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204290 | ||||||
| chr16:23204300 | T | TATATATA others(29): Show |
1 | a0001c0002t0003g0280 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(40): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204300 | ||||||
| chr16:23204302 | T | TATATATA others(19): Show |
1 | a0001c0001t0005g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1078-5423_1078-542 others(30): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204302 | ||||||
| chr16:23204304 | T | TATATATA others(23): Show |
1 | a0001c0001t0005g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(34): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204304 | ||||||
| chr16:23204310 | T | TATATATA others(11): Show |
1 | a0001c0002t0003g0278 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1078-5423_1078-542 others(22): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204310 | ||||||
| chr16:23204310 | TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0069 a0001c0002t0004g0284 |
2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1078-5438_1078-541 others(30): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204310 | ||||||
| chr16:23204310 | TATATATA others(21): Show |
T | 1 | a0001c0009t0017g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1078-5438_1078-541 others(32): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204310 | ||||||
| chr16:23204312 | TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0008 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1078-5436_1078-541 others(30): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204312 | ||||||
| chr16:23204314 | T | C | 1 | a0001c0002t0003g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1078-5436T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204314 | |||||||
| chr16:23204314 | T | TATATATA others(11): Show |
1 | a0001c0001t0005g0137 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1078-5419_1078-541 others(22): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204314 | ||||||
| chr16:23204316 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1078-5434T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204316 | |||||||
| chr16:23204318 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1078-5432T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204318 | |||||||
| chr16:23204318 | TATATATA others(11): Show |
T | 1 | a0001c0008t0001g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1078-5430_1078-541 others(22): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204318 | ||||||
| chr16:23204320 | T | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0211 others(1): Show |
4 | HG00621.hp1 HG00673.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-5430T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204320 | |||||||
| chr16:23204322 | T | G | 10 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0197 others(7): Show |
10 | HG00621.hp1 HG00673.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-5428T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204322 | |||||||
| chr16:23204322 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1078-5426_1078-541 others(18): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204322 | ||||||
| chr16:23204322 | TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1078-5426_1078-540 others(24): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204322 | ||||||
| chr16:23204322 | TATATATA others(15): Show |
T | 1 | a0001c0003t0002g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1078-5426_1078-540 others(26): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204322 | ||||||
| chr16:23204324 | T | C | 2 | a0001c0001t0005g0246 a0001c0002t0003g0255 |
2 | HG01261.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1078-5426T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204324 | |||||||
| chr16:23204324 | T | G | 22 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0100 others(19): Show |
22 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1078-5426T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204324 | |||||||
| chr16:23204324 | TATATATA others(5): Show |
T | 3 | a0001c0002t0004g0014 a0001c0002t0004g0265 a0001c0002t0004g0298 |
3 | NA18945.hp2 NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1078-5424_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204324 | ||||||
| chr16:23204324 | TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0041 a0001c0002t0004g0271 a0001c0003t0002g0011 |
4 | HG01256.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-5424_1078-541 others(18): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204324 | ||||||
| chr16:23204326 | T | C | 1 | a0001c0001t0005g0245 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1078-5424T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204326 | |||||||
| chr16:23204326 | T | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0071 others(38): Show |
41 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1078-5424T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204326 | |||||||
| chr16:23204326 | TATATATA others(3): Show |
T | 4 | a0001c0001t0001g0214 a0001c0003t0002g0238 a0001c0003t0002g0240 others(1): Show |
4 | HG00140.hp2 HG01993.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-5422_1078-541 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204326 | ||||||
| chr16:23204326 | TATATATA others(5): Show |
T | 2 | a0001c0001t0001g0167 a0001c0002t0004g0015 |
2 | NA19030.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1078-5422_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204326 | ||||||
| chr16:23204326 | TATATATA others(7): Show |
T | 1 | a0001c0001t0006g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1078-5422_1078-540 others(18): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204326 | ||||||
| chr16:23204326 | TATATATA others(9): Show |
T | 2 | a0001c0002t0004g0014 a0001c0002t0004g0015 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1078-5422_1078-540 others(20): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204326 | ||||||
| chr16:23204328 | T | C | 1 | a0001c0003t0002g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-5422T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204328 | |||||||
| chr16:23204328 | T | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0059 others(64): Show |
67 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-5422T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204328 | |||||||
| chr16:23204328 | TATATATA others(1): Show |
T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0074 others(6): Show |
9 | HG00423.hp1 HG00544.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078-5420_1078-541 others(12): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204328 | ||||||
| chr16:23204328 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1078-5420_1078-541 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204328 | ||||||
| chr16:23204328 | TATATATA others(5): Show |
T | 1 | a0001c0002t0004g0263 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1078-5420_1078-540 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204328 | ||||||
| chr16:23204330 | T | C | 1 | a0001c0001t0005g0247 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1078-5420T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204330 | |||||||
| chr16:23204330 | T | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0040 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1078-5420T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204330 | |||||||
| chr16:23204330 | T | TAGAGAGA others(5): Show |
1 | a0001c0002t0003g0260 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1078-5419_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204330 | ||||||
| chr16:23204330 | TATATAG | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0121 others(1): Show |
4 | HG01358.hp1 HG03195.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-5418_1078-541 others(10): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204330 | ||||||
| chr16:23204330 | TATATAGA others(5): Show |
T | 1 | a0001c0002t0004g0270 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1078-5418_1078-540 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204330 | ||||||
| chr16:23204330 | TATATAGA others(7): Show |
T | 1 | a0001c0002t0004g0254 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1078-5418_1078-540 others(18): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204330 | ||||||
| chr16:23204332 | T | C | 6 | a0001c0001t0005g0164 a0001c0001t0005g0233 a0001c0002t0003g0016 others(3): Show |
6 | HG01175.hp2 HG02080.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-5418T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204332 | |||||||
| chr16:23204332 | T | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(129): Show |
136 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1078-5418T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204332 | |||||||
| chr16:23204332 | T | TACATATA others(25): Show |
1 | a0001c0002t0003g0288 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(36): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(19): Show |
1 | a0001c0003t0002g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(30): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(23): Show |
1 | a0001c0001t0005g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(34): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(21): Show |
1 | a0001c0001t0005g0007 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(32): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(23): Show |
1 | a0001c0001t0005g0128 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(34): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(27): Show |
1 | a0001c0002t0003g0289 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(25): Show |
1 | a0001c0002t0003g0003 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(36): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(27): Show |
1 | a0001c0002t0003g0286 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TACATATA others(27): Show |
1 | a0001c0002t0003g0275 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TAGAGAGA others(3): Show |
3 | a0001c0001t0001g0045 a0001c0002t0003g0258 a0001c0002t0004g0257 |
3 | HG01257.hp2 HG02293.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1078-5417_1078-541 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | T | TAGAGAGA others(9): Show |
1 | a0001c0002t0003g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1078-5417_1078-541 others(20): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204332 | TATAGAG | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0218 others(1): Show |
4 | HG00597.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-5416_1078-541 others(10): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204332 | ||||||
| chr16:23204334 | T | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1078-5416T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204334 | |||||||
| chr16:23204334 | T | TACATATA others(29): Show |
1 | a0001c0002t0003g0276 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(40): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TACATATA others(25): Show |
1 | a0001c0001t0005g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(36): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TACATATA others(27): Show |
1 | a0001c0002t0003g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TACATATA others(29): Show |
1 | a0001c0003t0002g0171 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(40): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TAGAGAGA others(3): Show |
1 | a0001c0002t0004g0256 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1078-5386_1078-537 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATAGAGA others(5): Show |
1 | a0001c0002t0003g0001 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATAGA others(9): Show |
1 | a0001c0002t0003g0259 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(20): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATAGA others(11): Show |
1 | a0001c0002t0003g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(22): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0044 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(16): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(11): Show |
1 | a0001c0002t0003g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(22): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(19): Show |
1 | a0001c0001t0005g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(30): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(17): Show |
1 | a0001c0002t0003g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(28): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(25): Show |
1 | a0001c0001t0005g0245 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(36): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(21): Show |
1 | a0001c0001t0005g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(32): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(27): Show |
1 | a0001c0002t0003g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(27): Show |
1 | a0001c0001t0005g0247 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(21): Show |
1 | a0001c0003t0002g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(32): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(25): Show |
2 | a0001c0002t0003g0016 a0001c0002t0003g0274 |
2 | HG02080.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1078-5415_1078-541 others(36): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(23): Show |
1 | a0001c0001t0005g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(34): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | T | TATATATA others(27): Show |
1 | a0001c0002t0003g0294 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1078-5415_1078-541 others(38): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204334 | TAGAGAGA others(3): Show |
T | 1 | a0001c0001t0001g0020 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1078-5386_1078-537 others(14): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23204334 | ||||||
| chr16:23204336 | G | T | 9 | a0001c0001t0001g0122 a0001c0001t0001g0225 a0001c0001t0005g0137 others(6): Show |
9 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-5414G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204336 | |||||||
| chr16:23204338 | G | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0005g0137 others(1): Show |
4 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-5412G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204338 | |||||||
| chr16:23204340 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0005g0137 |
3 | HG00733.hp2 HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1078-5410G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204340 | |||||||
| chr16:23204342 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1078-5408G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204342 | |||||||
| chr16:23204344 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0156 |
4 | HG00642.hp2 HG00735.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-5406G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204344 | |||||||
| chr16:23204497 | A | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
133 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1078-5253A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204497 | |||||||
| chr16:23204845 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1078-4905C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204845 | |||||||
| chr16:23204846 | G | A | 1 | a0001c0009t0005g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078-4904G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204846 | |||||||
| chr16:23204893 | G | A | 1 | a0001c0003t0002g0184 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1078-4857G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23204893 | |||||||
| chr16:23205266 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4484A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205266 | |||||||
| chr16:23205270 | T | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4480T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205270 | |||||||
| chr16:23205271 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4479A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205271 | |||||||
| chr16:23205272 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4478C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205272 | |||||||
| chr16:23205274 | G | A | 1 | a0001c0004t0005g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1078-4476G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205274 | |||||||
| chr16:23205275 | T | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4475T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205275 | |||||||
| chr16:23205284 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4466A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205284 | |||||||
| chr16:23205286 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4464A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205286 | |||||||
| chr16:23205287 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4463A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205287 | |||||||
| chr16:23205290 | C | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4460C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205290 | |||||||
| chr16:23205292 | T | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4458T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205292 | |||||||
| chr16:23205293 | T | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4457T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205293 | |||||||
| chr16:23205303 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4447C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205303 | |||||||
| chr16:23205305 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4445C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205305 | |||||||
| chr16:23205306 | A | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4444A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205306 | |||||||
| chr16:23205311 | T | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4439T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205311 | |||||||
| chr16:23205312 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4438C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205312 | |||||||
| chr16:23205314 | A | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4436A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205314 | |||||||
| chr16:23205315 | C | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4435C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205315 | |||||||
| chr16:23205322 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4428A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205322 | |||||||
| chr16:23205323 | C | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4427C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205323 | |||||||
| chr16:23205325 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4425C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205325 | |||||||
| chr16:23205326 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4424C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205326 | |||||||
| chr16:23205328 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4422A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205328 | |||||||
| chr16:23205329 | C | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4421C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205329 | |||||||
| chr16:23205331 | G | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4419G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205331 | |||||||
| chr16:23205332 | T | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4418T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205332 | |||||||
| chr16:23205335 | G | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4415G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205335 | |||||||
| chr16:23205339 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4411A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205339 | |||||||
| chr16:23205342 | C | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4408C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205342 | |||||||
| chr16:23205343 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4407C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205343 | |||||||
| chr16:23205353 | G | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4397G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205353 | |||||||
| chr16:23205354 | G | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4396G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205354 | |||||||
| chr16:23205355 | G | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4395G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205355 | |||||||
| chr16:23205356 | T | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4394T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205356 | |||||||
| chr16:23205359 | T | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4391T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205359 | |||||||
| chr16:23205360 | G | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4390G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205360 | |||||||
| chr16:23205363 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4387A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205363 | |||||||
| chr16:23205365 | G | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4385G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205365 | |||||||
| chr16:23205366 | G | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4384G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205366 | |||||||
| chr16:23205367 | G | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4383G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205367 | |||||||
| chr16:23205370 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4380C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205370 | |||||||
| chr16:23205371 | T | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4379T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205371 | |||||||
| chr16:23205373 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4377A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205373 | |||||||
| chr16:23205380 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4370C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205380 | |||||||
| chr16:23205381 | T | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4369T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205381 | |||||||
| chr16:23205382 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4368A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205382 | |||||||
| chr16:23205383 | G | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4367G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205383 | |||||||
| chr16:23205384 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4366A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205384 | |||||||
| chr16:23205387 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4363C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205387 | |||||||
| chr16:23205388 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4362C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205388 | |||||||
| chr16:23205389 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4361C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205389 | |||||||
| chr16:23205390 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4360A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205390 | |||||||
| chr16:23205391 | A | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4359A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205391 | |||||||
| chr16:23205393 | G | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4357G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205393 | |||||||
| chr16:23205394 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4356C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205394 | |||||||
| chr16:23205401 | A | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4349A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205401 | |||||||
| chr16:23205403 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4347C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205403 | |||||||
| chr16:23205409 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4341C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205409 | |||||||
| chr16:23205411 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4339A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205411 | |||||||
| chr16:23205412 | T | G | 2 | a0001c0003t0002g0191 a0002c0006t0007g0029 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1078-4338T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205412 | |||||||
| chr16:23205423 | A | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4327A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205423 | |||||||
| chr16:23205424 | G | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4326G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205424 | |||||||
| chr16:23205425 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4325C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205425 | |||||||
| chr16:23205432 | C | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4318C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205432 | |||||||
| chr16:23205435 | T | A | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4315T>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205435 | |||||||
| chr16:23205440 | C | A | 1 | a0001c0001t0005g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1078-4310C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205440 | |||||||
| chr16:23205445 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4305C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205445 | |||||||
| chr16:23205453 | T | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4297T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205453 | |||||||
| chr16:23205463 | C | T | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4287C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205463 | |||||||
| chr16:23205464 | A | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4286A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205464 | |||||||
| chr16:23205468 | A | C | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4282A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205468 | |||||||
| chr16:23205469 | G | A | 1 | a0001c0012t0008g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1078-4281G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205469 | |||||||
| chr16:23205475 | A | G | 1 | a0001c0002t0003g0274 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1078-4275A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205475 | |||||||
| chr16:23205703 | G | GA | 45 | a0001c0001t0001g0232 a0001c0001t0005g0007 a0001c0001t0005g0119 others(42): Show |
52 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1078-4032dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23205703 | ||||||
| chr16:23205703 | GA | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
132 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1078-4032delA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23205703 | ||||||
| chr16:23205719 | G | T | 1 | a0001c0009t0005g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078-4031G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205719 | |||||||
| chr16:23205764 | G | A | 1 | a0001c0009t0017g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1078-3986G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205764 | |||||||
| chr16:23205772 | C | T | 1 | a0007c0011t0005g0058 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078-3978C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205772 | |||||||
| chr16:23205854 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1078-3896C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23205854 | |||||||
| chr16:23206081 | C | T | 45 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(42): Show |
52 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1078-3669C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206081 | |||||||
| chr16:23206159 | A | AG | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1078-3590dupG | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23206159 | ||||||
| chr16:23206231 | G | A | 2 | a0001c0003t0002g0183 a0001c0003t0002g0187 |
2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1078-3519G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206231 | |||||||
| chr16:23206434 | C | G | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1078-3316C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206434 | |||||||
| chr16:23206509 | G | A | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1078-3241G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206509 | |||||||
| chr16:23206525 | G | A | 45 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(42): Show |
52 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1078-3225G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206525 | |||||||
| chr16:23206688 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1078-3062A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206688 | |||||||
| chr16:23206755 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1078-2995G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206755 | |||||||
| chr16:23206810 | C | G | 1 | a0002c0010t0003g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1078-2940C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206810 | |||||||
| chr16:23206959 | G | A | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1078-2791G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23206959 | |||||||
| chr16:23207099 | C | T | 1 | a0001c0001t0005g0247 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1078-2651C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207099 | |||||||
| chr16:23207187 | G | A | 1 | a0001c0004t0005g0057 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1078-2563G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207187 | |||||||
| chr16:23207300 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1078-2450A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207300 | |||||||
| chr16:23207370 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1078-2380G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207370 | |||||||
| chr16:23207682 | A | G | 3 | a0001c0001t0012g0228 a0001c0008t0001g0018 a0001c0008t0001g0033 |
3 | HG00099.hp1 HG01123.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1078-2068A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207682 | |||||||
| chr16:23207740 | G | A | 1 | a0001c0002t0003g0281 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1078-2010G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207740 | |||||||
| chr16:23207889 | T | G | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1078-1861T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207889 | |||||||
| chr16:23207930 | C | T | 1 | a0001c0002t0003g0278 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1078-1820C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207930 | |||||||
| chr16:23207948 | T | C | 1 | a0001c0003t0002g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1078-1802T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207948 | |||||||
| chr16:23207951 | C | G | 21 | a0001c0003t0002g0011 a0001c0003t0002g0050 a0001c0003t0002g0095 others(18): Show |
22 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1078-1799C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23207951 | |||||||
| chr16:23208180 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1078-1570C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208180 | |||||||
| chr16:23208294 | C | T | 5 | a0001c0001t0001g0244 a0001c0002t0001g0063 a0001c0002t0004g0268 others(2): Show |
5 | HG01981.hp1 HG02273.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-1456C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208294 | |||||||
| chr16:23208315 | C | G | 1 | a0001c0009t0005g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078-1435C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208315 | |||||||
| chr16:23208355 | A | C | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1078-1395A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208355 | |||||||
| chr16:23208503 | G | A | 1 | a0001c0001t0005g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1078-1247G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208503 | |||||||
| chr16:23208634 | G | A | 50 | a0001c0001t0001g0182 a0001c0003t0002g0009 a0001c0003t0002g0011 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1078-1116G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208634 | |||||||
| chr16:23208782 | C | T | 1 | a0001c0001t0009g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1078-968C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208782 | |||||||
| chr16:23208892 | G | A | 44 | a0001c0001t0001g0202 a0001c0001t0005g0007 a0001c0001t0005g0119 others(41): Show |
51 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-858G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208892 | |||||||
| chr16:23208935 | C | G | 1 | a0001c0001t0008g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1078-815C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23208935 | |||||||
| chr16:23209114 | A | G | 1 | a0001c0002t0004g0284 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1078-636A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209114 | |||||||
| chr16:23209206 | C | T | 1 | a0001c0003t0002g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1078-544C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209206 | |||||||
| chr16:23209292 | TTCCTGTC others(118): Show |
T | 1 | a0001c0002t0004g0298 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1078-454_1078-330d others(2): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23209292 | ||||||
| chr16:23209414 | C | T | 1 | a0001c0001t0012g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1078-336C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209414 | |||||||
| chr16:23209434 | C | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1078-316C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209434 | |||||||
| chr16:23209467 | A | ATATCTTT others(118): Show |
1 | a0001c0002t0004g0298 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1078-277_1078-276i others(127): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 23209467 | ||||||
| chr16:23209518 | G | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1078-232G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209518 | |||||||
| chr16:23209521 | C | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1078-229C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209521 | |||||||
| chr16:23209590 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1078-160C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209590 | |||||||
| chr16:23209708 | C | T | 1 | a0001c0002t0004g0290 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1078-42C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209708 | |||||||
| chr16:23209721 | G | A | 1 | a0002c0006t0007g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078-29G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209721 | |||||||
| chr16:23209862 | A | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1176+14A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23209862 | |||||||
| chr16:23209917 | A | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
238 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1176+69A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23209917 | |||||||
| chr16:23209942 | A | G | 1 | a0001c0003t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1176+94A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23209942 | |||||||
| chr16:23210050 | G | A | 1 | a0001c0015t0001g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1176+202G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210050 | |||||||
| chr16:23210058 | T | C | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1176+210T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210058 | |||||||
| chr16:23210064 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1176+216A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210064 | |||||||
| chr16:23210086 | G | A | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1176+238G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210086 | |||||||
| chr16:23210128 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1176+280G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210128 | |||||||
| chr16:23210196 | T | G | 228 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(225): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1176+348T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210196 | |||||||
| chr16:23210203 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0144 others(3): Show |
8 | HG00733.hp1 HG02258.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1176+355G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210203 | |||||||
| chr16:23210371 | T | C | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1176+523T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210371 | |||||||
| chr16:23210400 | A | G | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1176+552A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210400 | |||||||
| chr16:23210476 | G | A | 11 | a0001c0002t0004g0014 a0001c0002t0004g0015 a0001c0002t0004g0254 others(8): Show |
13 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1176+628G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210476 | |||||||
| chr16:23210486 | G | A | 1 | a0001c0009t0005g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1176+638G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210486 | |||||||
| chr16:23210489 | T | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0144 others(20): Show |
26 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1176+641T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210489 | |||||||
| chr16:23210515 | C | A | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1176+667C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210515 | |||||||
| chr16:23210639 | G | A | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1176+791G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210639 | |||||||
| chr16:23210759 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1176+911T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210759 | |||||||
| chr16:23210841 | G | T | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1176+993G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210841 | |||||||
| chr16:23210967 | G | A | 1 | a0001c0007t0001g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1177-1067G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210967 | |||||||
| chr16:23210974 | C | G | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-1060C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210974 | |||||||
| chr16:23210997 | C | G | 41 | a0001c0001t0005g0007 a0001c0001t0005g0119 a0001c0001t0005g0128 others(38): Show |
48 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1177-1037C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210997 | |||||||
| chr16:23211044 | TA | T | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-983delA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23211044 | ||||||
| chr16:23211095 | A | G | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-939A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211095 | |||||||
| chr16:23211103 | G | A | 11 | a0001c0002t0004g0014 a0001c0002t0004g0015 a0001c0002t0004g0254 others(8): Show |
13 | HG00280.hp1 HG00544.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1177-931G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211103 | |||||||
| chr16:23211239 | T | G | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-795T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211239 | |||||||
| chr16:23211249 | C | T | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-785C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211249 | |||||||
| chr16:23211265 | C | T | 2 | a0001c0001t0012g0228 a0001c0008t0001g0018 |
2 | HG01123.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1177-769C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211265 | |||||||
| chr16:23211303 | T | C | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-731T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211303 | |||||||
| chr16:23211354 | G | A | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-680G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211354 | |||||||
| chr16:23211492 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1177-542C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211492 | |||||||
| chr16:23211635 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1177-399C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211635 | |||||||
| chr16:23211837 | G | A | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-197G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211837 | |||||||
| chr16:23211880 | C | T | 1 | a0001c0003t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1177-154C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211880 | |||||||
| chr16:23211888 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1177-146T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211888 | |||||||
| chr16:23211912 | G | T | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-122G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211912 | |||||||
| chr16:23211941 | G | A | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-93G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211941 | |||||||
| chr16:23211945 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1177-89G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211945 | |||||||
| chr16:23211979 | T | C | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1177-55T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211979 | |||||||
| chr16:23212251 | G | A | 1 | a0001c0002t0004g0267 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1294+100G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 8/12 | chr16 | 23212251 | |||||||
| chr16:23212344 | C | G | 1 | a0001c0001t0005g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1294+193C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 8/12 | chr16 | 23212344 | |||||||
| chr16:23212403 | C | G | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1294+252C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 8/12 | chr16 | 23212403 | |||||||
| chr16:23212785 | T | C | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1373+29T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 9/12 | chr16 | 23212785 | |||||||
| chr16:23212968 | C | T | 1 | a0001c0009t0005g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1431+74C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 10/12 | chr16 | 23212968 | |||||||
| chr16:23213041 | C | T | 1 | a0001c0002t0003g0278 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1432-61C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 10/12 | chr16 | 23213041 | |||||||
| chr16:23213095 | G | A | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
splice_region_variant&intron_variant | LOW | c.1432-7G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 10/12 | chr16 | 23213095 | |||||||
| chr16:23213196 | T | G | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1493+33T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213196 | |||||||
| chr16:23213252 | C | CT | 13 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0001c0001t0001g0098 others(10): Show |
13 | HG00741.hp2 HG01261.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.1493+110dupT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23213252 | ||||||
| chr16:23213252 | CT | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0088 a0001c0001t0001g0109 others(5): Show |
8 | HG01257.hp2 HG02683.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1493+110delT | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23213252 | ||||||
| chr16:23213273 | T | TA | 5 | a0001c0003t0002g0094 a0001c0003t0002g0097 a0001c0003t0002g0161 others(2): Show |
5 | HG02723.hp2 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493+111dupA | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23213273 | ||||||
| chr16:23213273 | T | TTA | 44 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(41): Show |
46 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1493+110_1493+111i others(4): Show |
SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213273 | |||||||
| chr16:23213284 | A | C | 5 | a0001c0001t0001g0244 a0001c0002t0001g0063 a0001c0002t0004g0268 others(2): Show |
5 | HG01981.hp1 HG02273.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493+121A>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213284 | |||||||
| chr16:23213377 | T | C | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1493+214T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213377 | |||||||
| chr16:23213400 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1493+237G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213400 | |||||||
| chr16:23213459 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1493+296C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213459 | |||||||
| chr16:23213720 | G | T | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1493+557G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213720 | |||||||
| chr16:23213726 | C | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0215 |
2 | HG00621.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1493+563C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213726 | |||||||
| chr16:23213929 | C | T | 1 | a0002c0010t0003g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1493+766C>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23213929 | |||||||
| chr16:23214530 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1494-182A>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23214530 | |||||||
| chr16:23214663 | A | G | 50 | a0001c0003t0002g0009 a0001c0003t0002g0011 a0001c0003t0002g0050 others(47): Show |
52 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1494-49A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 11/12 | chr16 | 23214663 | |||||||
| chr16:23214797 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG00558.hp1 HG02015.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1569+10G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 12/12 | chr16 | 23214797 | |||||||
| chr16:23214927 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0129 |
2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1569+140G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 12/12 | chr16 | 23214927 | |||||||
| chr16:23215074 | T | C | 1 | a0001c0002t0003g0285 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1570-15T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 12/12 | chr16 | 23215074 | |||||||
| chr16:23215080 | G | A | 1 | a0007c0011t0005g0058 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1570-9G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 12/12 | chr16 | 23215080 |