Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 649 | 311 | 86 | 70 | 97 | 14 | 42 | 62 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0002 | 0/0 | 649 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0003 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0004 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0005 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0006 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0007 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1950 | 186 | 56 | 34 | 60 | 4 | 31 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0002 | 0/0 | 1950 | 60 | 4 | 20 | 27 | 2 | 7 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0003 | 0/1 | 1950 | 44 | 17 | 10 | 8 | 4 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0004 | 0/0 | 1950 | 6 | 1 | 2 | 1 | 2 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0005 | 0/0 | 1950 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0006 | 0/0 | 1950 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0007 | 0/0 | 1950 | 3 | 0 | 2 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0008 | 0/0 | 1950 | 2 | 0 | 1 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0009 | 0/0 | 1950 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0010 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0011 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0012 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0013 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0014 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0015 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0016 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0017 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| c0018 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1528 | 164 | 35 | 35 | 62 | 8 | 23 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0002 | 0/1 | 1528 | 44 | 18 | 10 | 7 | 4 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0003 | 0/0 | 1528 | 35 | 1 | 15 | 12 | 1 | 6 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0004 | 0/0 | 1528 | 22 | 3 | 4 | 13 | 1 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0005 | 0/0 | 1528 | 18 | 7 | 4 | 3 | 0 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0006 | 0/0 | 1528 | 12 | 12 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0007 | 0/0 | 1528 | 8 | 7 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0008 | 0/0 | 1528 | 6 | 6 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0009 | 0/0 | 1528 | 3 | 0 | 0 | 0 | 0 | 3 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0010 | 0/0 | 1528 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0011 | 0/0 | 1528 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0012 | 0/0 | 1528 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0013 | 0/0 | 1528 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0014 | 0/0 | 1528 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0015 | 0/0 | 1528 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0016 | 0/0 | 1528 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| t0017 | 0/0 | 1528 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1950 | 186 | 56 | 34 | 60 | 4 | 31 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002 | 0/0 | 1950 | 60 | 4 | 20 | 27 | 2 | 7 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0003 | 0/1 | 1950 | 44 | 17 | 10 | 8 | 4 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0004 | 0/0 | 1950 | 6 | 1 | 2 | 1 | 2 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0005 | 0/0 | 1950 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0007 | 0/0 | 1950 | 3 | 0 | 2 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0008 | 0/0 | 1950 | 2 | 0 | 1 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0009 | 0/0 | 1950 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0012 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0015 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0017 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0002c0006 | 0/0 | 1950 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0002c0010 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0003c0018 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0004c0014 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0005c0013 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0006c0016 | 0/0 | 1950 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0007c0011 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | 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 | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0001t0005 | 0/0 | 3477 | 13 | 4 | 3 | 2 | 0 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0001t0006 | 0/0 | 3477 | 12 | 12 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0001t0008 | 0/0 | 3477 | 5 | 5 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0001t0009 | 0/0 | 3477 | 3 | 0 | 0 | 0 | 0 | 3 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0001t0012 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0001t0013 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002t0001 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002t0003 | 0/0 | 3477 | 34 | 0 | 15 | 12 | 1 | 6 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002t0004 | 0/0 | 3477 | 22 | 3 | 4 | 13 | 1 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002t0014 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002t0015 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0002t0016 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0003t0002 | 0/1 | 3477 | 43 | 17 | 10 | 7 | 4 | 4 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0003t0010 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0004t0001 | 0/0 | 3477 | 2 | 0 | 0 | 0 | 2 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0004t0005 | 0/0 | 3477 | 3 | 1 | 1 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0004t0011 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0005t0007 | 0/0 | 3477 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0007t0001 | 0/0 | 3477 | 3 | 0 | 2 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0008t0001 | 0/0 | 3477 | 2 | 0 | 1 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0009t0005 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0009t0017 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0012t0008 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0015t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0001c0017t0002 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0002c0006t0007 | 0/0 | 3477 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0002c0010t0003 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0003c0018t0001 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0004c0014t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0005c0013t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0006c0016t0001 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| a0007c0011t0005 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | copy fasta | chr16 | 23177745 | 23221883 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | 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 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0033 | 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 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0038 | 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 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0063 | 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 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0076 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0103 | 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 |
| a0001c0001t0001g0106 | 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 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0112 | 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 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0128 | 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 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0154 | 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 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0169 | 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 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0167 | 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 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0001t0013g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0257 | 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 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0015g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0002t0016g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0138 | 0/0 | 1 | 1 | 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 | 1 | 0 | 0 | 0 | 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 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0002g0173 | 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 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0003t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0004t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0251 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0005t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0007t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0007t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0008t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0008t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0009t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0009t0017g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0012t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0015t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0001c0017t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0006t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0006t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0006t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0002c0010t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0003c0018t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0004c0014t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0005c0013t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0006c0016t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| a0007c0011t0005g0051 | 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 | g0026 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0047 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00140 | hp2 | a0001 | c0007 | t0001 | g0049 | EUR | GBR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0271 | EUR | FIN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0304 | EUR | FIN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0300 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00423 | hp2 | a0006 | c0016 | t0001 | g0073 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0274 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0302 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0162 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0090 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0091 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0097 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0284 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01081 | hp2 | a0001 | c0004 | t0011 | g0044 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0308 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01106 | hp1 | a0001 | c0007 | t0001 | g0045 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0309 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01167 | hp2 | a0001 | c0005 | t0007 | g0253 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0170 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0288 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0289 | AMR | PUR | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0046 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0260 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0257 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0291 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0189 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0263 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0187 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0185 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0048 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0225 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01891 | hp2 | a0001 | c0005 | t0007 | g0255 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0243 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0188 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0295 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0262 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0278 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0270 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02055 | hp2 | a0001 | c0005 | t0007 | g0254 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0310 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0306 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02083 | hp1 | a0001 | c0015 | t0001 | g0066 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02145 | hp2 | a0001 | c0012 | t0008 | g0181 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02165 | hp2 | a0001 | c0002 | t0015 | g0290 | EAS | CDX | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0138 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0156 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0273 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0261 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0259 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0285 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0258 | AMR | PEL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0221 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0245 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0277 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02622 | hp1 | a0002 | c0006 | t0007 | g0024 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0235 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0231 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0303 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0312 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0092 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0307 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0242 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0139 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02896 | hp1 | a0002 | c0010 | t0003 | g0025 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0186 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0089 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0198 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0159 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0251 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03130 | hp1 | a0001 | c0005 | t0007 | g0252 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0141 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03225 | hp1 | a0001 | c0009 | t0017 | g0223 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0115 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0113 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0140 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0043 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0240 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0202 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | ESN | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0313 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03579 | hp2 | a0001 | c0002 | t0014 | g0279 | AFR | MSL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0287 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0206 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0301 | SAS | PJL | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG03942 | hp2 | a0001 | c0001 | t0009 | g0241 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0249 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0230 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0298 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0293 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0296 | SAS | STU | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0173 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0244 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18939 | hp1 | a0001 | c0004 | t0005 | g0050 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18941 | hp1 | a0001 | c0003 | t0010 | g0042 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0268 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0269 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0299 | 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 | g0164 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0280 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18967 | hp1 | a0004 | c0014 | t0001 | g0069 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0305 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18971 | hp2 | a0001 | c0002 | t0004 | g0267 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0201 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0281 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA18998 | hp2 | a0001 | c0002 | t0004 | g0276 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19001 | hp1 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0256 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0264 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0096 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0286 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0297 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0275 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19081 | hp1 | a0001 | c0002 | t0016 | g0283 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0165 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19091 | hp1 | a0005 | c0013 | t0001 | g0182 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | JPT | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0272 | AFR | ASW | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0143 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0142 | EUR | TSI | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01123 | hp1 | a0001 | c0008 | t0001 | g0009 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG01123 | hp2 | a0001 | c0004 | t0005 | g0008 | AMR | CLM | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0194 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0171 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02486 | hp1 | a0002 | c0006 | t0007 | g0022 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02486 | hp2 | a0003 | c0018 | t0001 | g0228 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02559 | hp1 | a0002 | c0006 | t0007 | g0023 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20300 | hp1 | a0007 | c0011 | t0005 | g0051 | AFR | USA | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA21309 | hp1 | a0001 | c0017 | t0002 | g0224 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| NA21309 | hp2 | a0001 | c0009 | t0005 | g0039 | AFR | LWK | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0137 | REF | REF | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | SCNN1G_chr16_23177745_23221883 | SCNN1G | chr16 | 23177745 | 23221883 |
| 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 | a0003 | 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 | a0006 | 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 | a0005 | 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 | a0004 | 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 |
| 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 | a0001c0002a0001c0004a0001c0005others(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 | a0001c0002a0001c0004a0001c0005others(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 | a0001c0004a0001c0007a0001c0009others(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 | a0001c0003a0001c0005a0001c0017others(1): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 |
| 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 | a0001c0002t0003a0001c0002t0004a0001c0002t0014others(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 | a0001c0003t0002a0001c0003t0010a0001c0005t0007others(2): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0003t0002a0001c0003t0010a0001c0005t0007others(2): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0003t0002a0001c0003t0010a0001c0005t0007others(2): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0005a0001c0002t0003a0001c0002t0015others(9): Show | 107 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(104): 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 | a0001c0003t0002a0001c0003t0010a0001c0005t0007others(2): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0005a0001c0002t0003a0001c0002t0015others(9): Show | 107 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(104): 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 | a0001c0003t0002a0001c0003t0010a0001c0005t0007others(2): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0005a0001c0002t0003a0001c0002t0015others(9): Show | 107 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(104): 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 | a0001c0003t0002a0001c0003t0010a0001c0005t0007others(2): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0008a0001c0009t0017a0001c0012t0008 | 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 |
| 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 | a0001c0004t0005g0008 | 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 | a0001c0008t0001g0009 | 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 | 64 | a0001c0001t0013g0313a0001c0002t0003g0007a0001c0002t0003g0257others(61): 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 | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(7): 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021 | 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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | a0001c0008t0001g0009a0001c0008t0001g0026 | 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 | a0001c0001t0001g0246a0001c0001t0005g0247a0001c0001t0005g0248others(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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024 | 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 | 62 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(59): 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 | a0001c0003t0002g0244a0001c0003t0002g0245 | 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 | a0001c0004t0005g0008a0001c0008t0001g0009a0001c0008t0001g0026 | 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 | a0001c0003t0002g0242a0001c0003t0002g0243 | 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 | a0001c0004t0005g0008 | 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 | 70 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(67): 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 | a0001c0005t0007g0251a0001c0005t0007g0252a0001c0005t0007g0253others(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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0009g0241 | 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | a0001c0001t0001g0006 | 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0030others(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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | 70 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(67): 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 | a0001c0002t0004g0311 | 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 | 63 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(60): 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 | 70 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(67): 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0034 | 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(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 | 63 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(60): 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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | a0001c0009t0005g0039 | 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | a0001c0001t0001g0040 | 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | 67 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(64): 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 | a0001c0002t0004g0256 | 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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | a0001c0004t0005g0008 | 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 | a0001c0003t0002g0240 | 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 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239 | 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 | 74 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(71): 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 | 9 | a0001c0002t0003g0303a0001c0002t0003g0304a0001c0002t0003g0305others(6): 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 | a0001c0003t0002g0043a0001c0003t0010g0042a0001c0004t0005g0008others(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 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0002t0003g0257 | 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 | a0001c0001t0001g0041 | 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 | a0001c0005t0007g0251a0001c0005t0007g0252a0001c0005t0007g0253others(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 | 62 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(59): 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 | 62 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(59): 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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | a0001c0008t0001g0009a0001c0008t0001g0026a0002c0006t0007g0022others(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 | a0001c0004t0005g0008 | 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 | a0001c0009t0005g0039a0001c0009t0017g0223a0001c0017t0002g0224 | 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 | a0001c0001t0008g0029 | 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 | a0001c0002t0004g0312 | 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 | 72 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(69): 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 | a0001c0008t0001g0026 | 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 | a0001c0002t0003g0260a0001c0002t0003g0261a0001c0002t0003g0262others(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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0050others(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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0050others(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 | a0001c0001t0001g0222 | 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 | a0001c0002t0003g0257 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0005 | 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 | a0001c0002t0003g0264 | 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 | a0001c0004t0005g0008 | 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 | a0001c0008t0001g0009a0001c0008t0001g0026a0002c0006t0007g0022others(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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | 40 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(37): 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 | a0001c0002t0003g0280a0001c0003t0002g0240 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0219 | 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 | a0001c0004t0005g0008 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0002t0003g0257 | 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 | 80 | a0001c0002t0001g0056a0001c0002t0003g0007a0001c0002t0003g0257others(77): 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 | a0001c0001t0001g0057 | 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 | 70 | a0001c0002t0001g0056a0001c0002t0003g0007a0001c0002t0003g0257others(67): 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 | a0001c0001t0001g0058 | 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 | 72 | a0001c0002t0001g0056a0001c0002t0003g0007a0001c0002t0003g0257others(69): 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 | a0001c0008t0001g0009a0001c0008t0001g0026a0002c0006t0007g0022others(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 | a0001c0001t0001g0005 | 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 | a0001c0017t0002g0224 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0001t0001g0006a0001c0001t0001g0208a0001c0001t0001g0209others(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 | a0001c0001t0001g0059 | 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 | a0002c0006t0007g0023a0002c0006t0007g0024 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0001t0001g0027a0001c0001t0001g0055a0001c0001t0001g0160others(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 | a0001c0001t0001g0040a0001c0001t0001g0197a0001c0001t0001g0199others(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 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0203others(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 | 99 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(96): 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 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0226others(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 | a0001c0001t0006g0060a0001c0001t0006g0225 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0002t0003g0291 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0003t0002g0097 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0050others(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 | a0001c0001t0001g0160a0001c0001t0001g0161 | 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 | 40 | a0001c0002t0003g0007a0001c0002t0003g0257a0001c0002t0003g0260others(37): 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0003t0002g0159 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021 | 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 | a0007c0011t0005g0051 | 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 | a0001c0004t0005g0008 | 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 | 80 | a0001c0002t0001g0056a0001c0002t0003g0007a0001c0002t0003g0257others(77): 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0008t0001g0009a0001c0008t0001g0026 | 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 | a0001c0002t0004g0312 | 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 | a0001c0001t0001g0001a0001c0001t0001g0158 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0002t0003g0257 | 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 | 64 | a0001c0002t0001g0056a0001c0002t0003g0007a0001c0002t0003g0257others(61): 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 | a0001c0002t0004g0312 | 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 | a0002c0006t0007g0022a0002c0006t0007g0023a0002c0006t0007g0024others(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 | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(89): 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0034others(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 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0099others(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 | a0001c0009t0017g0223 | 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 | a0001c0001t0001g0157a0001c0004t0001g0047a0001c0004t0001g0048others(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 | 66 | a0001c0002t0001g0056a0001c0002t0003g0007a0001c0002t0003g0257others(63): 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 | a0001c0003t0002g0240 | 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 | a0002c0010t0003g0025 | 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 | a0001c0009t0017g0223 | 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 | a0001c0002t0004g0312 | 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 | 140 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(137): 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 | a0001c0001t0001g0183 | 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 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0005g0008others(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 | a0001c0017t0002g0224 | 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 | a0001c0009t0005g0039a0001c0009t0017g0223a0001c0017t0002g0224 | 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 | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(173): 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 | a0001c0009t0017g0223 | 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 | a0001c0002t0004g0292a0001c0004t0001g0047a0001c0004t0005g0050 | 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 | 112 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0070others(109): Show | 115 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(112): 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 | a0001c0001t0001g0227 | 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 | a0001c0004t0005g0221 | 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 | a0001c0004t0005g0008a0007c0011t0005g0051 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(128): 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 | a0001c0002t0003g0310 | 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 | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(182): Show | 188 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.913+1013C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195287 | ||||||
| chr16:23195291
|
C | T | 41 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(38): Show | 42 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(39): 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 | a0001c0008t0001g0026 | 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 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(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 | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(234): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): 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 | a0002c0010t0003g0025 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(128): 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 | 184 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(181): 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 | |||||
| chr16:23195965
|
G | A | 1 | a0001c0003t0002g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.914-1299G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23195965 | ||||||
| chr16:23196153
|
G | T | 48 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(45): Show | 49 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(46): 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 | a0001c0012t0008g0181 | 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 | a0001c0004t0005g0221 | 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 | a0002c0006t0007g0023a0002c0006t0007g0024 | 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 | 48 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(45): Show | 49 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(46): 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 | 3 | a0001c0002t0004g0265a0001c0002t0004g0274a0001c0002t0004g0275 | 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 | a0001c0002t0015g0290 | 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 | a0001c0001t0001g0158 | 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 | 49 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(46): Show | 50 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(47): 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 | a0001c0001t0012g0230a0001c0008t0001g0009a0001c0008t0001g0026 | 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 | 49 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(46): Show | 50 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.914-468T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 5/12 | chr16 | 23196796 | ||||||
| chr16:23196811
|
A | G | 49 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(46): Show | 50 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(47): 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 | a0001c0004t0005g0221 | 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 | a0007c0011t0005g0051 | 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 | a0002c0010t0003g0025 | 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 | a0001c0002t0004g0258a0001c0002t0004g0259 | 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 | 235 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(232): Show | 239 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(236): 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 | a0001c0004t0005g0221 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0018 | 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 | a0001c0002t0015g0290 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0117 | 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 | a0002c0010t0003g0025 | 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 | 13 | a0001c0002t0004g0256a0001c0002t0004g0265a0001c0002t0004g0266others(10): 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(128): 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 | a0001c0004t0005g0221 | 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 | a0001c0001t0005g0235a0001c0001t0005g0236a0001c0003t0002g0096others(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 | a0001c0009t0017g0223 | 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 | a0001c0002t0003g0284 | 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 | a0001c0001t0001g0033a0001c0001t0001g0062a0001c0001t0001g0112others(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 | 145 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(142): 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 | 55 | a0001c0001t0001g0184a0001c0001t0001g0237a0001c0001t0001g0238others(52): Show | 56 | HG00544.hp1 HG00597.hp2 HG00738.hp2 others(53): 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 | a0001c0001t0005g0247a0001c0002t0004g0266a0001c0002t0004g0276others(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 | a0001c0001t0006g0002a0001c0001t0006g0060a0001c0001t0006g0121others(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 | a0001c0001t0005g0247a0001c0001t0005g0248a0001c0001t0005g0249others(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 | 41 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(38): Show | 42 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(39): 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 | a0001c0003t0002g0097a0001c0003t0002g0143a0001c0003t0002g0188 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(128): 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0012g0230 | 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 | a0001c0001t0001g0085 | 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 | 186 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(183): 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 | a0001c0002t0003g0298 | 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 | 52 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(49): 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 | a0001c0001t0001g0063a0006c0016t0001g0073 | 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 | a0001c0002t0004g0266 | 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 | 52 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(49): 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 | 53 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(50): 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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(233): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1077+3271C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23200698 | ||||||
| chr16:23200868
|
C | G | 53 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(50): 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 | 22 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0145others(19): 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 | a0001c0001t0001g0149a0001c0001t0001g0168a0001c0001t0001g0179others(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 | a0001c0017t0002g0224 | 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 | a0001c0001t0009g0198a0001c0001t0009g0206 | 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 | a0001c0003t0002g0138 | 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 | a0001c0001t0005g0074 | 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 | a0001c0001t0001g0238 | 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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(100): 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 | 82 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0040others(79): 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 | a0001c0003t0002g0143a0001c0003t0002g0188a0001c0007t0001g0045others(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 | a0001c0002t0003g0285 | 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 | a0001c0003t0002g0091 | 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 | a0001c0001t0008g0028a0001c0001t0008g0029a0001c0001t0008g0030others(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 | a0001c0004t0005g0221 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0057others(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 | 27 | a0001c0001t0001g0093a0001c0001t0001g0124a0001c0001t0001g0148others(24): 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 | 47 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(44): 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 | a0001c0001t0001g0035a0001c0003t0002g0142a0002c0010t0003g0025 | 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 | a0001c0003t0002g0142 | 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 | a0001c0001t0001g0169 | 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 | a0001c0004t0005g0221 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0012g0230a0001c0008t0001g0009a0001c0008t0001g0026 | 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 | a0001c0004t0005g0050 | 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 | a0001c0001t0001g0107 | 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 | a0001c0004t0001g0048a0001c0004t0011g0044 | 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 | a0001c0001t0001g0070 | 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 | a0001c0002t0003g0305 | 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 | 50 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(47): Show | 51 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(48): 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 | a0001c0001t0013g0313 | 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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(233): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): 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 | a0001c0001t0001g0034a0001c0001t0001g0103 | 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 | 182 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(179): Show | 186 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(183): 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 | 43 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0037others(40): 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 | a0001c0001t0001g0099a0001c0001t0001g0246a0001c0004t0005g0221others(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 | 11 | a0001c0002t0004g0256a0001c0002t0004g0265a0001c0002t0004g0266others(8): 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 | a0001c0002t0003g0298 | 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 | a0001c0001t0001g0183 | 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 | a0001c0002t0003g0308a0001c0002t0014g0279 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0001g0080others(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 | 32 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0068others(29): Show | 32 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(29): 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 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0064others(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 | 30 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(27): 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 | a0001c0001t0001g0006a0001c0001t0001g0123a0001c0001t0001g0209others(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 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0059others(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 | a0001c0001t0001g0093a0001c0001t0001g0161a0001c0001t0008g0029others(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 | a0001c0004t0005g0008a0001c0004t0005g0221 | 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 | a0001c0002t0003g0310 | 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 | a0001c0004t0005g0050 | 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 | a0001c0001t0001g0053a0001c0002t0015g0290 | 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 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(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 | a0001c0002t0003g0264 | 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 | a0001c0002t0003g0286 | 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 | a0001c0001t0005g0116 | 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 | a0001c0001t0005g0172 | 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 | a0001c0002t0003g0284 | 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 | a0001c0001t0001g0062a0001c0002t0004g0292 | 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 | a0001c0009t0017g0223 | 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 | a0001c0001t0001g0127 | 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 | a0001c0002t0003g0293 | 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 | a0001c0001t0005g0136 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0104 | 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 | a0001c0008t0001g0009 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0213others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0199others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0195 | 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 | a0001c0003t0002g0245 | 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 | a0001c0001t0005g0248a0001c0002t0003g0257 | 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 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0095others(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 | a0001c0002t0004g0267a0001c0002t0004g0268a0001c0002t0004g0311 | 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 | a0001c0001t0001g0034a0001c0002t0004g0277a0001c0003t0002g0004 | 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 | a0001c0001t0005g0247 | 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 | 42 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0071others(39): Show | 42 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(39): 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 | a0001c0001t0001g0216a0001c0003t0002g0240a0001c0003t0002g0242others(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 | a0001c0001t0001g0169a0001c0002t0004g0275 | 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 | a0001c0001t0006g0060 | 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 | a0001c0002t0004g0270a0001c0002t0004g0274 | 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 | a0001c0003t0002g0156 | 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 | 68 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0053others(65): Show | 68 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(65): 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 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0067others(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 | a0001c0001t0001g0005 | 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 | a0001c0002t0004g0265 | 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 | a0001c0001t0005g0249 | 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 | 98 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0041others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(96): 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 | a0001c0002t0003g0262 | 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 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0118others(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 | a0001c0002t0004g0276 | 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 | a0001c0002t0004g0256 | 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 | a0001c0001t0005g0166a0001c0001t0005g0235a0001c0002t0003g0280others(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 | 135 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(132): Show | 137 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(134): 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 | a0001c0002t0003g0299 | 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 | a0001c0003t0002g0096 | 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 | a0001c0001t0005g0236 | 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 | a0001c0001t0005g0113 | 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 | a0001c0001t0005g0125 | 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 | a0001c0002t0003g0300 | 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 | a0001c0002t0003g0294 | 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 | a0001c0002t0003g0297 | 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 | a0001c0002t0003g0281 | 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 | a0001c0001t0001g0038a0001c0002t0003g0260a0001c0002t0004g0259 | 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 | a0001c0002t0003g0287 | 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 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0220others(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 | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(181): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): 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 | a0001c0002t0003g0282 | 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 | a0001c0001t0005g0114 | 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 | a0001c0002t0003g0296 | 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 | a0001c0003t0002g0173 | 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 | a0001c0002t0004g0258 | 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 | a0001c0002t0003g0288 | 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 | a0001c0002t0003g0261 | 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 | a0001c0002t0003g0263 | 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 | a0001c0001t0001g0037 | 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 | a0001c0002t0003g0293 | 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 | a0001c0001t0005g0248 | 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 | a0001c0002t0003g0257 | 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 | a0001c0001t0005g0247 | 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 | a0001c0001t0005g0235 | 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 | a0001c0002t0003g0298 | 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 | a0001c0001t0005g0249 | 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 | a0001c0003t0002g0156 | 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 | a0001c0002t0003g0280a0001c0002t0003g0306 | 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 | a0001c0001t0005g0166 | 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 | a0001c0002t0003g0305 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0119a0001c0001t0001g0227a0001c0001t0005g0136others(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 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0005g0136others(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 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0005g0136 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0001a0001c0001t0001g0081a0001c0001t0001g0158 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(128): 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 | a0001c0001t0001g0095 | 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 | a0001c0009t0005g0039 | 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 | a0001c0003t0002g0186 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0004t0005g0221 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0003t0002g0193a0002c0006t0007g0022 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0001t0005g0235 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0002t0003g0280 | 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 | a0001c0012t0008g0181 | 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 | a0001c0002t0003g0280 | 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 | 51 | a0001c0001t0001g0234a0001c0001t0005g0113a0001c0001t0005g0114others(48): 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 | 130 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(127): 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 | a0001c0009t0005g0039 | 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 | a0001c0009t0017g0223 | 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 | a0007c0011t0005g0051 | 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 | a0001c0001t0001g0227 | 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 | 51 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(48): 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 | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(250): Show | 257 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(254): 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 | a0001c0003t0002g0185a0001c0003t0002g0189 | 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(130): 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(130): 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 | 51 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(48): 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0211 | 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 | a0002c0010t0003g0025 | 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 | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(304): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0005g0249 | 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 | a0001c0004t0005g0050 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0012g0230a0001c0008t0001g0009a0001c0008t0001g0026 | 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 | a0001c0002t0003g0289 | 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(130): 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 | a0001c0002t0003g0284 | 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 | a0001c0003t0002g0091 | 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 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0090others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0246a0001c0002t0001g0056a0001c0002t0004g0272others(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 | a0001c0009t0005g0039 | 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 | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(182): 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 | a0001c0001t0005g0166 | 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 | 52 | a0001c0001t0001g0184a0001c0003t0002g0004a0001c0003t0002g0043others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0009g0206 | 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 | 50 | a0001c0001t0001g0204a0001c0001t0005g0113a0001c0001t0005g0114others(47): 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 | a0001c0001t0008g0030 | 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 | a0001c0002t0004g0292 | 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 | a0001c0003t0002g0185 | 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 | a0001c0002t0004g0311 | 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 | a0001c0001t0012g0230 | 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 | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(234): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): 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 | a0001c0002t0004g0311 | 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 | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(234): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1078-232G>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 6/12 | chr16 | 23209518 | ||||||
| chr16:23209521
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(234): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): 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 | a0001c0001t0001g0072 | 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 | a0001c0002t0004g0301 | 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 | a0002c0006t0007g0022 | 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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(233): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1176+14A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23209862 | ||||||
| chr16:23209917
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(232): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): 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 | a0001c0003t0002g0097 | 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 | a0001c0015t0001g0066 | 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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(233): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): 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 | a0001c0001t0001g0195 | 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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(233): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): 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 | a0001c0001t0001g0128 | 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 | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(236): Show | 243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1176+348T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210196 | ||||||
| chr16:23210203
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0145others(4): 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 | 238 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(235): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1176+523T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210371 | ||||||
| chr16:23210400
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(235): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1176+552A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210400 | ||||||
| chr16:23210476
|
G | A | 13 | a0001c0002t0004g0256a0001c0002t0004g0265a0001c0002t0004g0266others(10): 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 | a0001c0009t0005g0039 | 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 | 24 | a0001c0001t0001g0003a0001c0001t0001g0122a0001c0001t0001g0145others(21): 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 | 238 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(235): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1176+667C>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210515 | ||||||
| chr16:23210639
|
G | A | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0149 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0007t0001g0046 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1177-1060C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23210974 | ||||||
| chr16:23210997
|
C | G | 47 | a0001c0001t0005g0113a0001c0001t0005g0114a0001c0001t0005g0116others(44): 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1177-939A>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211095 | ||||||
| chr16:23211103
|
G | A | 13 | a0001c0002t0004g0256a0001c0002t0004g0265a0001c0002t0004g0266others(10): 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1177-795T>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211239 | ||||||
| chr16:23211249
|
C | T | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0012g0230a0001c0008t0001g0009 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1177-731T>C | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211303 | ||||||
| chr16:23211354
|
G | A | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0086 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0003t0002g0202 | 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 | a0001c0001t0001g0197 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1177-122G>T | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 7/12 | chr16 | 23211912 | ||||||
| chr16:23211941
|
G | A | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0062 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0002t0004g0271 | 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 | a0001c0001t0005g0074 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1294+252C>G | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 8/12 | chr16 | 23212403 | ||||||
| chr16:23212785
|
T | C | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0009t0005g0039 | 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 | a0001c0002t0003g0284 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0093others(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 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0105others(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 | a0001c0003t0002g0089a0001c0003t0002g0092a0001c0003t0002g0163others(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 | 46 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0090others(43): Show | 47 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(44): 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 | a0001c0001t0001g0246a0001c0002t0001g0056a0001c0002t0004g0272others(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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0123 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0213a0001c0001t0001g0217 | 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 | a0002c0010t0003g0025 | 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 | a0001c0001t0001g0078 | 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 | 52 | a0001c0003t0002g0004a0001c0003t0002g0043a0001c0003t0002g0089others(49): Show | 53 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(50): 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 | a0001c0001t0001g0065a0001c0001t0001g0099a0001c0001t0001g0100others(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 | a0001c0001t0001g0076a0001c0001t0001g0126 | 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 | a0001c0002t0003g0293 | 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 | a0007c0011t0005g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1570-9G>A | SCNN1G | ENSG00000166828.3 | transcript | ENST00000300061.3 | protein_coding | 12/12 | chr16 | 23215080 |