| geneid | 6339 |
|---|---|
| ensemblid | ENSG00000162572.21 |
| hgncid | 10601 |
| symbol | SCNN1D |
| name | sodium channel epithelial 1 subunit delta |
| refseq_nuc | NM_001130413.4 |
| refseq_prot | NP_001123885.2 |
| ensembl_nuc | ENST00000379116.10 |
| ensembl_prot | ENSP00000368411.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 1280436 |
| end | 1292025 |
| strand | + |
| ver | v1.2 |
| region | chr1:1280436-1292025 |
| region5000 | chr1:1275436-1297025 |
| regionname0 | SCNN1D_chr1_1280436_1292025 |
| regionname5000 | SCNN1D_chr1_1275436_1297025 |
| 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 | 802 | 99 | 17 | 38 | 21 | 11 | 10 | 14 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002 | 0/0 | 802 | 96 | 14 | 14 | 53 | 1 | 14 | 35 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0003 | 0/0 | 802 | 30 | 3 | 3 | 23 | 0 | 1 | 16 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004 | 0/0 | 802 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005 | 0/0 | 802 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0006 | 0/0 | 802 | 6 | 0 | 2 | 4 | 0 | 0 | 3 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0007 | 0/0 | 802 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0008 | 0/0 | 802 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0009 | 0/0 | 802 | 4 | 0 | 0 | 3 | 0 | 1 | 2 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0010 | 0/0 | 802 | 3 | 1 | 0 | 2 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0011 | 0/0 | 125 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0012 | 0/0 | 802 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0013 | 0/0 | 802 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0014 | 0/0 | 802 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0015 | 0/0 | 796 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0016 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0017 | 0/0 | 802 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0018 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0019 | 0/0 | 802 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0020 | 0/0 | 588 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0021 | 0/0 | 802 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0022 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0023 | 0/0 | 802 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0024 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0025 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0026 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0027 | 0/0 | 802 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0028 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0029 | 0/0 | 134 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0030 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2409 | 85 | 15 | 33 | 19 | 8 | 8 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0002 | 0/0 | 2409 | 54 | 0 | 6 | 43 | 0 | 5 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0003 | 0/0 | 2409 | 41 | 14 | 8 | 9 | 1 | 9 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0004 | 0/0 | 2409 | 29 | 2 | 3 | 23 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0005 | 0/0 | 2409 | 6 | 4 | 2 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0006 | 0/0 | 2409 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0007 | 0/0 | 2409 | 5 | 5 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0008 | 0/0 | 2409 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0009 | 0/0 | 2409 | 4 | 0 | 4 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0010 | 0/0 | 2409 | 4 | 0 | 2 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0011 | 0/0 | 2409 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0012 | 0/0 | 2409 | 3 | 0 | 0 | 0 | 2 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0013 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0014 | 0/0 | 2409 | 2 | 0 | 0 | 1 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0015 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0016 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0017 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0018 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0019 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0020 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0021 | 0/0 | 2409 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0022 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0023 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0024 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0025 | 0/0 | 2408 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0026 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0027 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0028 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0029 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0030 | 0/0 | 2428 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0031 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0032 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0033 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0034 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0035 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0036 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0037 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0038 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0039 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0040 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0041 | 0/0 | 2404 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0042 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0043 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0044 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0045 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0046 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| c0047 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| 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 | 1/1 | 642 | 169 | 31 | 45 | 57 | 10 | 24 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0002 | 0/0 | 642 | 45 | 2 | 16 | 18 | 2 | 7 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0003 | 0/0 | 642 | 33 | 4 | 3 | 25 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0004 | 0/0 | 642 | 15 | 15 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0005 | 0/0 | 642 | 6 | 0 | 0 | 6 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0006 | 0/0 | 641 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0007 | 0/0 | 642 | 4 | 0 | 2 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0008 | 0/0 | 642 | 4 | 2 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0009 | 0/0 | 642 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0010 | 0/0 | 641 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0011 | 0/0 | 642 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0012 | 0/0 | 641 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| t0013 | 0/0 | 642 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| 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 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2409 | 85 | 15 | 33 | 19 | 8 | 8 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0009 | 0/0 | 2409 | 4 | 0 | 4 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0012 | 0/0 | 2409 | 3 | 0 | 0 | 0 | 2 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0018 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0020 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0036 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0046 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0047 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0002 | 0/0 | 2409 | 54 | 0 | 6 | 43 | 0 | 5 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0003 | 0/0 | 2409 | 41 | 14 | 8 | 9 | 1 | 9 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0028 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0003c0004 | 0/0 | 2409 | 29 | 2 | 3 | 23 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0003c0034 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004c0005 | 0/0 | 2409 | 6 | 4 | 2 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004c0008 | 0/0 | 2409 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0011 | 0/0 | 2409 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0016 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0017 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0006c0010 | 0/0 | 2409 | 4 | 0 | 2 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0006c0015 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0007c0006 | 0/0 | 2409 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0008c0007 | 0/0 | 2409 | 5 | 5 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0009c0013 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0009c0014 | 0/0 | 2409 | 2 | 0 | 0 | 1 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0010c0019 | 0/0 | 2409 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0010c0035 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0011c0023 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0012c0022 | 0/0 | 2409 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0013c0042 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0013c0043 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0014c0021 | 0/0 | 2409 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0015c0037 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0016c0031 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0017c0029 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0018c0027 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0019c0026 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0020c0030 | 0/0 | 2428 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0021c0032 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0022c0040 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0023c0045 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0024c0033 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0025c0044 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0026c0041 | 0/0 | 2404 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0027c0039 | 0/0 | 2409 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0028c0038 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0029c0025 | 0/0 | 2408 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0030c0024 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3050 | 59 | 13 | 28 | 2 | 6 | 8 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0001t0002 | 0/0 | 3050 | 20 | 1 | 4 | 13 | 2 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0001t0005 | 0/0 | 3050 | 4 | 0 | 0 | 4 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0001t0011 | 0/0 | 3050 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0009t0001 | 0/0 | 3050 | 4 | 0 | 4 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0012t0001 | 0/0 | 3050 | 3 | 0 | 0 | 0 | 2 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0018t0001 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0018t0005 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0020t0001 | 0/0 | 3050 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0036t0006 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0046t0001 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0001c0047t0001 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0002t0001 | 0/0 | 3050 | 53 | 0 | 6 | 42 | 0 | 5 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0002t0013 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0003t0001 | 0/0 | 3050 | 11 | 4 | 0 | 3 | 1 | 3 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0003t0002 | 0/0 | 3050 | 19 | 0 | 8 | 5 | 0 | 6 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0003t0004 | 0/0 | 3050 | 10 | 10 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0003t0005 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0002c0028t0001 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0003c0004t0003 | 0/0 | 3050 | 29 | 2 | 3 | 23 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0003c0034t0009 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004c0005t0002 | 0/0 | 3050 | 2 | 0 | 2 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004c0005t0006 | 0/0 | 3049 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004c0005t0010 | 0/0 | 3049 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0004c0008t0001 | 0/0 | 3050 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0011t0001 | 0/0 | 3050 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0016t0001 | 0/0 | 3050 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0017t0001 | 0/0 | 3050 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0005c0017t0002 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0006c0010t0007 | 0/0 | 3050 | 4 | 0 | 2 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0006c0015t0008 | 0/0 | 3050 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0007c0006t0001 | 0/0 | 3050 | 5 | 4 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0008c0007t0004 | 0/0 | 3050 | 5 | 5 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0009c0013t0001 | 0/0 | 3050 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0009c0014t0001 | 0/0 | 3050 | 2 | 0 | 0 | 1 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0010c0019t0003 | 0/0 | 3050 | 2 | 0 | 0 | 2 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0010c0035t0009 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0011c0023t0001 | 0/0 | 3050 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0012c0022t0006 | 0/0 | 3049 | 2 | 1 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0013c0042t0001 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0013c0043t0001 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0014c0021t0008 | 0/0 | 3050 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0015c0037t0001 | 0/0 | 3032 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0016c0031t0001 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0017c0029t0001 | 0/0 | 3050 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0018c0027t0001 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0019c0026t0001 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0020c0030t0002 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0021c0032t0002 | 0/0 | 3050 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0022c0040t0012 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0023c0045t0001 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0024c0033t0009 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0025c0044t0003 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0026c0041t0001 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0027c0039t0002 | 0/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0028c0038t0003 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0029c0025t0001 | 0/0 | 3049 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| a0030c0024t0001 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | copy fasta | chr1 | 1275436 | 1297025 |
| 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 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0011g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0001t0011g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0009t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0009t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0009t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0009t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0012t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0012t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0012t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0018t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0018t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0020t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0020t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0036t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0046t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0001c0047t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0002t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0003t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0002c0028t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0004t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0003c0034t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0005t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0005t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0005t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0005t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0005t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0005t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0008t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0008t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0008t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0004c0008t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0011t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0011t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0011t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0016t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0016t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0017t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0005c0017t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0006c0010t0007g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0006c0010t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0006c0010t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0006c0010t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0006c0015t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0006c0015t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0007c0006t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0007c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0007c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0007c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0007c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0008c0007t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0008c0007t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0008c0007t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0008c0007t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0008c0007t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0009c0013t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0009c0013t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0009c0014t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0009c0014t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0010c0019t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0010c0019t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0010c0035t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0011c0023t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0011c0023t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0012c0022t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0012c0022t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0013c0042t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0013c0043t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0014c0021t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0014c0021t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0015c0037t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0016c0031t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0017c0029t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0018c0027t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0019c0026t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0020c0030t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0021c0032t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0022c0040t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0023c0045t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0024c0033t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0025c0044t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0026c0041t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0027c0039t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0028c0038t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0029c0025t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| a0030c0024t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00099 | hp2 | a0001 | c0047 | t0001 | g0183 | EUR | GBR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | FIN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00423 | hp2 | a0002 | c0002 | t0013 | g0075 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00438 | hp1 | a0009 | c0013 | t0001 | g0040 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00558 | hp2 | a0003 | c0004 | t0003 | g0142 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0110 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00597 | hp2 | a0006 | c0010 | t0007 | g0273 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00639 | hp1 | a0001 | c0009 | t0001 | g0211 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00642 | hp1 | a0012 | c0022 | t0006 | g0132 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00673 | hp2 | a0002 | c0028 | t0001 | g0093 | EAS | CHS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00738 | hp1 | a0006 | c0010 | t0007 | g0270 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01069 | hp1 | a0005 | c0016 | t0001 | g0281 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01109 | hp1 | a0004 | c0008 | t0001 | g0241 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01109 | hp2 | a0003 | c0004 | t0003 | g0143 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01169 | hp1 | a0004 | c0005 | t0002 | g0028 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01169 | hp2 | a0001 | c0020 | t0001 | g0176 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0061 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01175 | hp2 | a0021 | c0032 | t0002 | g0039 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01243 | hp1 | a0007 | c0006 | t0001 | g0070 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01243 | hp2 | a0011 | c0023 | t0001 | g0264 | AMR | PUR | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0021 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01256 | hp1 | a0001 | c0009 | t0001 | g0210 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0012 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01257 | hp2 | a0001 | c0009 | t0001 | g0205 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01258 | hp1 | a0020 | c0030 | t0002 | g0103 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01346 | hp1 | a0003 | c0004 | t0003 | g0006 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01358 | hp1 | a0002 | c0003 | t0002 | g0024 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0107 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0267 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01496 | hp1 | a0006 | c0010 | t0007 | g0274 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0099 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01516 | hp1 | a0001 | c0012 | t0001 | g0127 | EUR | IBS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0225 | EUR | IBS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01517 | hp2 | a0001 | c0012 | t0001 | g0131 | EUR | IBS | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01884 | hp1 | a0002 | c0003 | t0004 | g0119 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01884 | hp2 | a0002 | c0003 | t0004 | g0113 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01891 | hp2 | a0028 | c0038 | t0003 | g0283 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01928 | hp2 | a0002 | c0003 | t0002 | g0104 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01943 | hp2 | a0017 | c0029 | t0001 | g0048 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02015 | hp2 | a0010 | c0019 | t0003 | g0098 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02040 | hp2 | a0013 | c0043 | t0001 | g0147 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02071 | hp1 | a0001 | c0018 | t0001 | g0251 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02071 | hp2 | a0003 | c0004 | t0003 | g0150 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02074 | hp1 | a0003 | c0004 | t0003 | g0149 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02132 | hp1 | a0003 | c0004 | t0003 | g0220 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02135 | hp1 | a0003 | c0004 | t0003 | g0155 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02145 | hp2 | a0002 | c0003 | t0001 | g0069 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02155 | hp1 | a0010 | c0019 | t0003 | g0170 | EAS | CDX | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | CDX | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02165 | hp1 | a0003 | c0004 | t0003 | g0172 | EAS | CDX | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CDX | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02258 | hp1 | a0004 | c0008 | t0001 | g0239 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02258 | hp2 | a0004 | c0005 | t0006 | g0126 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02293 | hp1 | a0002 | c0003 | t0002 | g0027 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02300 | hp1 | a0001 | c0009 | t0001 | g0218 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02300 | hp2 | a0003 | c0004 | t0003 | g0106 | AMR | PEL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02451 | hp2 | a0007 | c0006 | t0001 | g0073 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02622 | hp1 | a0014 | c0021 | t0008 | g0272 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02622 | hp2 | a0005 | c0011 | t0001 | g0157 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0082 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02717 | hp2 | a0012 | c0022 | t0006 | g0269 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02723 | hp1 | a0002 | c0003 | t0004 | g0114 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02723 | hp2 | a0010 | c0035 | t0009 | g0280 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02809 | hp1 | a0007 | c0006 | t0001 | g0100 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02809 | hp2 | a0002 | c0003 | t0004 | g0121 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02818 | hp1 | a0002 | c0003 | t0004 | g0111 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02886 | hp1 | a0002 | c0003 | t0004 | g0116 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02886 | hp2 | a0005 | c0011 | t0001 | g0158 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02895 | hp1 | a0005 | c0011 | t0001 | g0156 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02895 | hp2 | a0004 | c0005 | t0006 | g0128 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02896 | hp1 | a0003 | c0034 | t0009 | g0279 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02896 | hp2 | a0003 | c0004 | t0003 | g0148 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02922 | hp1 | a0008 | c0007 | t0004 | g0266 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02970 | hp1 | a0008 | c0007 | t0004 | g0285 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02970 | hp2 | a0002 | c0003 | t0004 | g0118 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02976 | hp1 | a0002 | c0003 | t0004 | g0115 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02976 | hp2 | a0004 | c0008 | t0001 | g0240 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0105 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03139 | hp1 | a0004 | c0008 | t0001 | g0247 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03139 | hp2 | a0008 | c0007 | t0004 | g0286 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03195 | hp2 | a0008 | c0007 | t0004 | g0287 | AFR | ESN | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03209 | hp1 | a0001 | c0020 | t0001 | g0263 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03209 | hp2 | a0004 | c0005 | t0010 | g0124 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0268 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0054 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03486 | hp1 | a0007 | c0006 | t0001 | g0072 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03486 | hp2 | a0007 | c0006 | t0001 | g0071 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03490 | hp1 | a0003 | c0004 | t0003 | g0145 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03490 | hp2 | a0019 | c0026 | t0001 | g0014 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03491 | hp1 | a0029 | c0025 | t0001 | g0256 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03491 | hp2 | a0002 | c0003 | t0002 | g0015 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03540 | hp1 | a0003 | c0004 | t0003 | g0141 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03540 | hp2 | a0002 | c0003 | t0004 | g0117 | AFR | GWD | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03579 | hp2 | a0004 | c0008 | t0001 | g0262 | AFR | MSL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03688 | hp1 | a0009 | c0014 | t0001 | g0050 | SAS | STU | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03688 | hp2 | a0002 | c0003 | t0002 | g0081 | SAS | STU | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0097 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0055 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03831 | hp2 | a0001 | c0046 | t0001 | g0259 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03942 | hp1 | a0023 | c0045 | t0001 | g0164 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG03942 | hp2 | a0027 | c0039 | t0002 | g0136 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG04184 | hp1 | a0015 | c0037 | t0001 | g0090 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG04184 | hp2 | a0001 | c0012 | t0001 | g0130 | SAS | BEB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG04199 | hp2 | a0002 | c0003 | t0002 | g0074 | SAS | STU | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0083 | SAS | STU | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | STU | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18522 | hp1 | a0001 | c0036 | t0006 | g0123 | AFR | YRI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18522 | hp2 | a0004 | c0005 | t0010 | g0125 | AFR | YRI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18612 | hp1 | a0003 | c0004 | t0003 | g0138 | EAS | CHB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | CHB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18747 | hp2 | a0026 | c0041 | t0001 | g0261 | EAS | CHB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18906 | hp1 | a0005 | c0017 | t0002 | g0288 | AFR | YRI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18906 | hp2 | a0024 | c0033 | t0009 | g0278 | AFR | YRI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18946 | hp2 | a0009 | c0014 | t0001 | g0009 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18954 | hp2 | a0006 | c0015 | t0008 | g0277 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18961 | hp1 | a0003 | c0004 | t0003 | g0007 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18964 | hp2 | a0003 | c0004 | t0003 | g0135 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18967 | hp2 | a0003 | c0004 | t0003 | g0152 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18970 | hp1 | a0003 | c0004 | t0003 | g0144 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18971 | hp2 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0032 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18975 | hp1 | a0006 | c0015 | t0008 | g0276 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18980 | hp1 | a0003 | c0004 | t0003 | g0171 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18980 | hp2 | a0018 | c0027 | t0001 | g0020 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18983 | hp2 | a0030 | c0024 | t0001 | g0051 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18995 | hp1 | a0002 | c0003 | t0002 | g0038 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18998 | hp1 | a0003 | c0004 | t0003 | g0154 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA18998 | hp2 | a0003 | c0004 | t0003 | g0153 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19002 | hp2 | a0001 | c0018 | t0005 | g0224 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19005 | hp1 | a0003 | c0004 | t0003 | g0137 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19007 | hp2 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19009 | hp2 | a0003 | c0004 | t0003 | g0134 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19043 | hp1 | a0002 | c0003 | t0004 | g0120 | AFR | LWK | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0091 | AFR | LWK | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19057 | hp1 | a0003 | c0004 | t0003 | g0146 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19057 | hp2 | a0003 | c0004 | t0003 | g0004 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19064 | hp1 | a0002 | c0003 | t0002 | g0122 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19067 | hp1 | a0006 | c0010 | t0007 | g0275 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19067 | hp2 | a0003 | c0004 | t0003 | g0133 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19070 | hp1 | a0003 | c0004 | t0003 | g0253 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19072 | hp1 | a0003 | c0004 | t0003 | g0139 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19072 | hp2 | a0002 | c0003 | t0005 | g0002 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19077 | hp1 | a0022 | c0040 | t0012 | g0159 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19079 | hp1 | a0009 | c0013 | t0001 | g0078 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19079 | hp2 | a0002 | c0003 | t0002 | g0101 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19082 | hp2 | a0016 | c0031 | t0001 | g0092 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19088 | hp1 | a0003 | c0004 | t0003 | g0151 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19240 | hp1 | a0014 | c0021 | t0008 | g0271 | AFR | YRI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA19240 | hp2 | a0005 | c0016 | t0001 | g0289 | AFR | YRI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA20805 | hp2 | a0002 | c0003 | t0001 | g0060 | EUR | TSI | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA20905 | hp1 | a0013 | c0042 | t0001 | g0129 | SAS | GIH | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01123 | hp1 | a0004 | c0005 | t0002 | g0022 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG01123 | hp2 | a0005 | c0017 | t0001 | g0282 | AMR | CLM | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02109 | hp2 | a0008 | c0007 | t0004 | g0284 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0112 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG02559 | hp2 | a0025 | c0044 | t0003 | g0257 | AFR | ACB | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG06807 | hp1 | a0011 | c0023 | t0001 | g0265 | AFR | USA | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | USA | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0215 | REF | REF | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0174 | REF | REF | SCNN1D_chr1_1275436_1297025 | SCNN1D | chr1 | 1275436 | 1297025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1281502
|
G | A | 1 | a0030 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.169G>A | p.Gly57Arg | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/18 | 395/3050 | 169/2409 | 57/802 | chr1 | 1281502 | ||
| chr1:1283904
|
AGGTGTGG others(67): Show |
A | 1 | a0029 | 1 | HG03491.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.352-73_352delGGTGT others(69): Show |
p.Glu118fs | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/18 | 352/2409 | 118/802 | chr1 | 1283904 | |||
| chr1:1284002
|
C | G | 1 | a0012 | 2 | HG00642.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.376C>G | p.Gln126Glu | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/18 | 602/3050 | 376/2409 | 126/802 | chr1 | 1284002 | ||
| chr1:1284002
|
C | T | 1 | a0011 | 2 | HG01243.hp2 HG06807.hp1 |
stop_gained | HIGH | c.376C>T | p.Gln126* | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/18 | 602/3050 | 376/2409 | 126/802 | chr1 | 1284002 | ||
| chr1:1285594
|
A | G | 1 | a0014 | 2 | HG02622.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.488A>G | p.Gln163Arg | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/18 | 714/3050 | 488/2409 | 163/802 | chr1 | 1285594 | ||
| chr1:1285621
|
A | G | 4 | a0005a0008a0012others(1): Show | 15 | HG00642.hp1 HG01069.hp1 HG01123.hp2 others(12): Show |
missense_variant | MODERATE | c.515A>G | p.Gln172Arg | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/18 | 741/3050 | 515/2409 | 172/802 | chr1 | 1285621 | ||
| chr1:1286119
|
CCTGGGGG others(11): Show |
C | 1 | a0015 | 1 | HG04184.hp1 | disruptive_inframe_deletion | MODERATE | c.753_770delCTGGGGGC others(10): Show |
p.Trp252_Leu257del | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/18 | 979/3050 | 753/2409 | 251/802 | chr1 | 1286119 | ||
| chr1:1286180
|
T | G | 1 | a0027 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.813T>G | p.Phe271Leu | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/18 | 1039/3050 | 813/2409 | 271/802 | chr1 | 1286180 | ||
| chr1:1286887
|
G | C | 11 | a0002a0007a0009others(8): Show | 113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
missense_variant | MODERATE | c.1031G>C | p.Arg344Pro | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 8/18 | 1257/3050 | 1031/2409 | 344/802 | chr1 | 1286887 | ||
| chr1:1286889
|
C | T | 1 | a0021 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1033C>T | p.His345Tyr | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 8/18 | 1259/3050 | 1033/2409 | 345/802 | chr1 | 1286889 | ||
| chr1:1287218
|
C | T | 1 | a0007 | 5 | HG01243.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.1229C>T | p.Ala410Val | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/18 | 1455/3050 | 1229/2409 | 410/802 | chr1 | 1287218 | ||
| chr1:1287578
|
C | T | 1 | a0006 | 6 | HG00597.hp2 HG00738.hp1 HG01496.hp1 others(3): Show |
missense_variant | MODERATE | c.1381C>T | p.Arg461Cys | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 10/18 | 1607/3050 | 1381/2409 | 461/802 | chr1 | 1287578 | ||
| chr1:1287727
|
C | T | 1 | a0016 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.1454C>T | p.Thr485Met | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 11/18 | 1680/3050 | 1454/2409 | 485/802 | chr1 | 1287727 | ||
| chr1:1287811
|
C | T | 1 | a0015 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1538C>T | p.Thr513Met | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 11/18 | 1764/3050 | 1538/2409 | 513/802 | chr1 | 1287811 | ||
| chr1:1288003
|
T | G | 1 | a0022 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.1628T>G | p.Val543Gly | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/18 | 1854/3050 | 1628/2409 | 543/802 | chr1 | 1288003 | ||
| chr1:1288005
|
G | C | 12 | a0002a0004a0007others(9): Show | 122 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
missense_variant | MODERATE | c.1630G>C | p.Glu544Gln | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/18 | 1856/3050 | 1630/2409 | 544/802 | chr1 | 1288005 | ||
| chr1:1290482
|
T | A | 1 | a0019 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1786T>A | p.Cys596Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 14/18 | 2012/3050 | 1786/2409 | 596/802 | chr1 | 1290482 | ||
| chr1:1290683
|
G | A | 4 | a0013a0018a0028others(1): Show | 5 | HG01891.hp2 HG02040.hp2 NA18980.hp2 others(2): Show |
missense_variant | MODERATE | c.1906G>A | p.Ala636Thr | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/18 | 2132/3050 | 1906/2409 | 636/802 | chr1 | 1290683 | ||
| chr1:1291120
|
G | C | 1 | a0025 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.2032G>C | p.Glu678Gln | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/18 | 2258/3050 | 2032/2409 | 678/802 | chr1 | 1291120 | ||
| chr1:1291123
|
G | A | 1 | a0015 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.2035G>A | p.Glu679Lys | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/18 | 2261/3050 | 2035/2409 | 679/802 | chr1 | 1291123 | ||
| chr1:1291132
|
G | A | 1 | a0023 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2044G>A | p.Val682Met | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/18 | 2270/3050 | 2044/2409 | 682/802 | chr1 | 1291132 | ||
| chr1:1291377
|
G | A | 6 | a0003a0010a0022others(3): Show | 37 | HG00558.hp2 HG01109.hp2 HG01346.hp1 others(34): Show |
missense_variant | MODERATE | c.2176G>A | p.Gly726Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2402/3050 | 2176/2409 | 726/802 | chr1 | 1291377 | ||
| chr1:1291471
|
C | T | 1 | a0008 | 5 | HG02109.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.2270C>T | p.Pro757Leu | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2496/3050 | 2270/2409 | 757/802 | chr1 | 1291471 | ||
| chr1:1291482
|
G | A | 1 | a0017 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.2281G>A | p.Gly761Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2507/3050 | 2281/2409 | 761/802 | chr1 | 1291482 | ||
| chr1:1291509
|
G | A | 5 | a0003a0022a0024others(2): Show | 34 | HG00558.hp2 HG01109.hp2 HG01346.hp1 others(31): Show |
missense_variant | MODERATE | c.2308G>A | p.Gly770Arg | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2534/3050 | 2308/2409 | 770/802 | chr1 | 1291509 | ||
| chr1:1291591
|
T | C | 2 | a0024a0025 | 2 | HG02559.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2390T>C | p.Leu797Pro | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2616/3050 | 2390/2409 | 797/802 | chr1 | 1291591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1281468
|
G | A | 1 | a0001c0009 | 4 | HG00639.hp1 HG01256.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.135G>A | p.Ser45Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/18 | 361/3050 | 135/2409 | 45/802 | chr1 | 1281468 | ||
| chr1:1281591
|
G | A | 1 | a0005c0011 | 3 | HG02622.hp2 HG02886.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.258G>A | p.Pro86Pro | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/18 | 484/3050 | 258/2409 | 86/802 | chr1 | 1281591 | ||
| chr1:1285574
|
G | A | 28 | a0001c0036a0002c0002a0002c0003others(25): Show | 146 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
synonymous_variant | LOW | c.468G>A | p.Ser156Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/18 | 694/3050 | 468/2409 | 156/802 | chr1 | 1285574 | ||
| chr1:1287201
|
C | T | 1 | a0001c0047 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1212C>T | p.Ile404Ile | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/18 | 1438/3050 | 1212/2409 | 404/802 | chr1 | 1287201 | ||
| chr1:1287980
|
C | T | 1 | a0001c0020 | 2 | HG01169.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1605C>T | p.Thr535Thr | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/18 | 1831/3050 | 1605/2409 | 535/802 | chr1 | 1287980 | ||
| chr1:1287983
|
C | T | 1 | a0001c0036 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1608C>T | p.Ala536Ala | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/18 | 1834/3050 | 1608/2409 | 536/802 | chr1 | 1287983 | ||
| chr1:1290912
|
G | A | 11 | a0001c0018a0002c0002a0002c0028others(8): Show | 68 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(65): Show |
synonymous_variant | LOW | c.1935G>A | p.Thr645Thr | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 16/18 | 2161/3050 | 1935/2409 | 645/802 | chr1 | 1290912 | ||
| chr1:1291122
|
G | A | 1 | a0002c0028 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.2034G>A | p.Glu678Glu | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/18 | 2260/3050 | 2034/2409 | 678/802 | chr1 | 1291122 | ||
| chr1:1291271
|
G | C | 2 | a0001c0012a0013c0042 | 4 | HG01516.hp1 HG01517.hp2 HG04184.hp2 others(1): Show |
synonymous_variant | LOW | c.2070G>C | p.Ser690Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2296/3050 | 2070/2409 | 690/802 | chr1 | 1291271 | ||
| chr1:1291310
|
C | T | 1 | a0001c0046 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.2109C>T | p.Ser703Ser | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 2335/3050 | 2109/2409 | 703/802 | chr1 | 1291310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1280469
|
A | T | 6 | a0003c0034t0009a0006c0010t0007a0006c0015t0008others(3): Show | 11 | HG00597.hp2 HG00738.hp1 HG01496.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-193A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/18 | 193 | chr1 | 1280469 | |||||
| chr1:1280471
|
A | T | 1 | a0001c0001t0011 | 2 | HG01433.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-191A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/18 | 191 | chr1 | 1280471 | |||||
| chr1:1291725
|
C | T | 1 | a0002c0002t0013 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 115 | chr1 | 1291725 | |||||
| chr1:1291731
|
TG | T | 5 | a0001c0036t0006a0004c0005t0006a0004c0005t0010others(2): Show | 8 | HG00642.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*125delG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 125 | INFO_REALIGN_3_PRIME | chr1 | 1291731 | ||||
| chr1:1291802
|
G | A | 3 | a0001c0001t0005a0001c0018t0005a0002c0003t0005 | 6 | NA19002.hp2 NA19056.hp2 NA19070.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*192G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 192 | chr1 | 1291802 | |||||
| chr1:1291816
|
A | G | 2 | a0002c0003t0004a0008c0007t0004 | 15 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*206A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 206 | chr1 | 1291816 | |||||
| chr1:1291862
|
G | A | 1 | a0004c0005t0010 | 2 | HG03209.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*252G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 252 | chr1 | 1291862 | |||||
| chr1:1291864
|
G | A | 11 | a0001c0001t0002a0001c0001t0005a0001c0018t0005others(8): Show | 55 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*254G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 254 | chr1 | 1291864 | |||||
| chr1:1291869
|
T | C | 8 | a0003c0004t0003a0003c0034t0009a0010c0019t0003others(5): Show | 37 | HG00558.hp2 HG01109.hp2 HG01346.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*259T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 18/18 | 259 | chr1 | 1291869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1280785
|
T | G | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.5+119T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1280785 | ||||||
| chr1:1280815
|
C | A | 121 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(118): Show | 121 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.5+149C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1280815 | ||||||
| chr1:1280878
|
G | A | 9 | a0001c0012t0001g0127a0001c0012t0001g0130a0001c0012t0001g0131others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.5+212G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1280878 | ||||||
| chr1:1280919
|
C | G | 1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5+253C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1280919 | ||||||
| chr1:1280990
|
G | A | 1 | a0002c0002t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6-236G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1280990 | ||||||
| chr1:1281090
|
A | G | 9 | a0005c0016t0001g0281a0005c0016t0001g0289a0005c0017t0001g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.6-136A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281090 | ||||||
| chr1:1281155
|
G | A | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.6-71G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281155 | ||||||
| chr1:1281156
|
A | G | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.6-70A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281156 | ||||||
| chr1:1281163
|
G | A | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.6-63G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281163 | ||||||
| chr1:1281168
|
TCTG | T | 121 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(118): Show | 121 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.6-57_6-55delCTG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281168 | ||||||
| chr1:1281172
|
G | T | 121 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(118): Show | 121 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.6-54G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281172 | ||||||
| chr1:1281201
|
G | C | 27 | a0001c0001t0002g0140a0003c0004t0003g0133a0003c0004t0003g0134others(24): Show | 27 | HG00558.hp2 HG01109.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.6-25G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 1/17 | chr1 | 1281201 | ||||||
| chr1:1281631
|
A | C | 61 | a0001c0001t0002g0140a0001c0001t0011g0267a0001c0001t0011g0268others(58): Show | 61 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.277+21A>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281631 | ||||||
| chr1:1281640
|
G | C | 49 | a0001c0001t0002g0140a0001c0001t0011g0267a0001c0001t0011g0268others(46): Show | 49 | HG00558.hp2 HG00642.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+30G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281640 | ||||||
| chr1:1281641
|
C | T | 11 | a0002c0003t0001g0112a0002c0003t0004g0111a0002c0003t0004g0113others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+31C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281641 | ||||||
| chr1:1281644
|
G | C | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.277+34G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281644 | ||||||
| chr1:1281658
|
G | A | 1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.277+48G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281658 | ||||||
| chr1:1281678
|
G | A | 13 | a0001c0001t0011g0267a0001c0001t0011g0268a0003c0034t0009g0279others(10): Show | 13 | HG00597.hp2 HG00738.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.277+68G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281678 | ||||||
| chr1:1281878
|
G | C | 50 | a0001c0001t0002g0140a0001c0001t0011g0267a0001c0001t0011g0268others(47): Show | 50 | HG00558.hp2 HG00642.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.277+268G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1281878 | ||||||
| chr1:1282070
|
G | A | 1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.278-172G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1282070 | ||||||
| chr1:1282076
|
G | A | 1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278-166G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1282076 | ||||||
| chr1:1282199
|
C | T | 1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.278-43C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 3/17 | chr1 | 1282199 | ||||||
| chr1:1282558
|
C | CCA | 171 | a0001c0001t0002g0140a0001c0001t0011g0267a0001c0001t0011g0268others(168): Show | 171 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.351+248_351+249dup others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1282558 | |||||
| chr1:1282559
|
C | CAT | 9 | a0005c0016t0001g0281a0005c0016t0001g0289a0005c0017t0001g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+245_351+246ins others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1282559 | |||||
| chr1:1282626
|
G | A | 3 | a0004c0005t0006g0126a0004c0005t0010g0124a0004c0005t0010g0125 | 3 | HG02258.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.351+311G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282626 | ||||||
| chr1:1282706
|
C | G | 1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.351+391C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282706 | ||||||
| chr1:1282706
|
C | T | 152 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0012t0001g0127others(149): Show | 152 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.351+391C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282706 | ||||||
| chr1:1282756
|
C | CT | 20 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0012t0001g0130others(17): Show | 20 | HG01069.hp1 HG01433.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+455dupT | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1282756 | |||||
| chr1:1282756
|
C | CTT | 9 | a0005c0016t0001g0289a0005c0017t0001g0282a0005c0017t0002g0288others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+454_351+455dup others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1282756 | |||||
| chr1:1282756
|
CT | C | 16 | a0001c0001t0001g0160a0002c0002t0001g0003a0002c0002t0001g0013others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+455delT | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1282756 | |||||
| chr1:1282783
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.351+468T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282783 | ||||||
| chr1:1282805
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.351+490T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282805 | ||||||
| chr1:1282809
|
G | A | 2 | a0001c0001t0011g0267a0001c0001t0011g0268 | 2 | HG01433.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.351+494G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282809 | ||||||
| chr1:1282838
|
C | T | 1 | a0004c0008t0001g0262 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.351+523C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282838 | ||||||
| chr1:1282900
|
C | CTGCCACC others(13): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.351+587_351+606dup others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1282900 | |||||
| chr1:1282954
|
G | A | 9 | a0001c0012t0001g0127a0001c0012t0001g0130a0001c0012t0001g0131others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+639G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1282954 | ||||||
| chr1:1283165
|
A | G | 3 | a0003c0034t0009g0279a0010c0035t0009g0280a0024c0033t0009g0278 | 3 | HG02723.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.352-813A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283165 | ||||||
| chr1:1283172
|
C | A | 1 | a0011c0023t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.352-806C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283172 | ||||||
| chr1:1283203
|
C | A | 1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.352-775C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283203 | ||||||
| chr1:1283275
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0002g0260a0001c0046t0001g0259others(1): Show | 4 | HG00735.hp1 HG02523.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-703C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283275 | ||||||
| chr1:1283373
|
C | T | 2 | a0001c0001t0005g0258a0001c0036t0006g0123 | 2 | NA18522.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.352-605C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283373 | ||||||
| chr1:1283414
|
C | T | 5 | a0006c0010t0007g0273a0006c0010t0007g0274a0006c0010t0007g0275others(2): Show | 5 | HG00597.hp2 HG01496.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-564C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283414 | ||||||
| chr1:1283420
|
C | T | 4 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-558C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283420 | ||||||
| chr1:1283452
|
A | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-526A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283452 | ||||||
| chr1:1283457
|
G | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-521G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283457 | ||||||
| chr1:1283458
|
G | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-520G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283458 | ||||||
| chr1:1283459
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-519G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283459 | ||||||
| chr1:1283461
|
G | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-517G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283461 | ||||||
| chr1:1283462
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-516G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283462 | ||||||
| chr1:1283463
|
C | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-515C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283463 | ||||||
| chr1:1283464
|
T | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-514T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283464 | ||||||
| chr1:1283467
|
G | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-511G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283467 | ||||||
| chr1:1283468
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-510G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283468 | ||||||
| chr1:1283469
|
C | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-509C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283469 | ||||||
| chr1:1283470
|
G | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-508G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283470 | ||||||
| chr1:1283470
|
G | GGGCGGAT others(11): Show |
1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.352-505_352-488dup others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 1283470 | |||||
| chr1:1283472
|
G | T | 26 | a0001c0001t0011g0268a0001c0012t0001g0127a0001c0012t0001g0130others(23): Show | 26 | HG00642.hp1 HG01069.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-506G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283472 | ||||||
| chr1:1283473
|
C | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-505C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283473 | ||||||
| chr1:1283482
|
T | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-496T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283482 | ||||||
| chr1:1283487
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-491T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283487 | ||||||
| chr1:1283488
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-490T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283488 | ||||||
| chr1:1283489
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-489G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283489 | ||||||
| chr1:1283490
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-488G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283490 | ||||||
| chr1:1283494
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-484T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283494 | ||||||
| chr1:1283495
|
T | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-483T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283495 | ||||||
| chr1:1283496
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-482T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283496 | ||||||
| chr1:1283499
|
G | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-479G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283499 | ||||||
| chr1:1283501
|
C | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-477C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283501 | ||||||
| chr1:1283503
|
A | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-475A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283503 | ||||||
| chr1:1283504
|
G | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-474G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283504 | ||||||
| chr1:1283505
|
C | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-473C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283505 | ||||||
| chr1:1283508
|
G | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-470G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283508 | ||||||
| chr1:1283510
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-468G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283510 | ||||||
| chr1:1283510
|
G | C | 25 | a0001c0001t0011g0268a0001c0012t0001g0127a0001c0012t0001g0130others(22): Show | 25 | HG00642.hp1 HG01069.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.352-468G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283510 | ||||||
| chr1:1283513
|
G | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-465G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283513 | ||||||
| chr1:1283516
|
T | C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-462T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283516 | ||||||
| chr1:1283521
|
A | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-457A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283521 | ||||||
| chr1:1283524
|
C | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-454C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283524 | ||||||
| chr1:1283525
|
C | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-453C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283525 | ||||||
| chr1:1283526
|
C | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-452C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283526 | ||||||
| chr1:1283527
|
C | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-451C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283527 | ||||||
| chr1:1283529
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-449T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283529 | ||||||
| chr1:1283530
|
C | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-448C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283530 | ||||||
| chr1:1283531
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-447T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283531 | ||||||
| chr1:1283532
|
C | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-446C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283532 | ||||||
| chr1:1283533
|
T | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-445T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283533 | ||||||
| chr1:1283534
|
A | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-444A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283534 | ||||||
| chr1:1283535
|
C | A | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-443C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283535 | ||||||
| chr1:1283536
|
T | G | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-442T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283536 | ||||||
| chr1:1283538
|
A | T | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.352-440A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283538 | ||||||
| chr1:1283590
|
C | G | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.352-388C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283590 | ||||||
| chr1:1283655
|
G | A | 4 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-323G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283655 | ||||||
| chr1:1283671
|
CTGGGCAA others(3): Show |
C | 1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.352-306_352-297del others(10): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283671 | ||||||
| chr1:1283684
|
G | A | 1 | a0024c0033t0009g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.352-294G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 4/17 | chr1 | 1283684 | ||||||
| chr1:1284095
|
C | T | 1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | splice_region_variant&intron_variant | LOW | c.464+5C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284095 | ||||||
| chr1:1284097
|
T | TG | 109 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.464+16dupG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284097 | |||||
| chr1:1284097
|
T | TGG | 18 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0023others(15): Show | 18 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.464+15_464+16dupGG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284097 | |||||
| chr1:1284104
|
G | T | 1 | a0011c0023t0001g0265 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.464+14G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284104 | ||||||
| chr1:1284105
|
G | GGGGTGAG others(118): Show |
2 | a0005c0017t0001g0282a0028c0038t0003g0283 | 2 | HG01123.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.464+16_464+17insGG others(123): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284105 | |||||
| chr1:1284105
|
G | GGGTGAGG others(56): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.464+16_464+17insGT others(61): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284105 | |||||
| chr1:1284116
|
TG | T | 7 | a0001c0001t0002g0255a0001c0012t0001g0127a0001c0012t0001g0130others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.464+33delG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284116 | |||||
| chr1:1284117
|
G | GGGGGGTT others(4): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.464+32_464+33insTT others(9): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284117 | |||||
| chr1:1284125
|
T | TGGGTGGG others(79): Show |
1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.464+40_464+41insGG others(84): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284125 | |||||
| chr1:1284136
|
G | GTTGGGTG others(1): Show |
4 | a0001c0036t0006g0123a0004c0005t0006g0128a0004c0005t0010g0124others(1): Show | 4 | HG02895.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+46_464+47insTT others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284136 | ||||||
| chr1:1284138
|
T | G | 5 | a0001c0036t0006g0123a0003c0004t0003g0133a0004c0005t0006g0128others(2): Show | 5 | HG02895.hp2 HG03209.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+48T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284138 | ||||||
| chr1:1284138
|
T | TGAGG | 4 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+49_464+50insAG others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284138 | |||||
| chr1:1284138
|
T | TGGGGGGG others(303): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.464+52_464+53insGG others(308): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284138 | |||||
| chr1:1284143
|
T | G | 1 | a0003c0004t0003g0133 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.464+53T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284143 | ||||||
| chr1:1284143
|
TCG | T | 15 | a0001c0001t0001g0252a0001c0001t0002g0161a0001c0001t0002g0163others(12): Show | 15 | HG00558.hp1 HG01346.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.464+54_464+55delCG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284143 | ||||||
| chr1:1284143
|
TCGGG | T | 6 | a0001c0001t0011g0268a0001c0012t0001g0127a0001c0012t0001g0130others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.464+54_464+57delCG others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284143 | ||||||
| chr1:1284144
|
C | G | 9 | a0001c0036t0006g0123a0002c0003t0002g0032a0004c0005t0006g0128others(6): Show | 9 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.464+54C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284144 | ||||||
| chr1:1284144
|
C | T | 2 | a0003c0004t0003g0133a0025c0044t0003g0257 | 2 | HG02559.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.464+54C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284144 | ||||||
| chr1:1284144
|
CG | C | 134 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0002g0140others(131): Show | 134 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.464+64delG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284144 | |||||
| chr1:1284144
|
CGG | C | 55 | a0001c0001t0001g0162a0001c0001t0001g0237a0001c0001t0001g0238others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.464+63_464+64delGG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284144 | |||||
| chr1:1284145
|
G | C | 1 | a0003c0004t0003g0133 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.464+55G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284145 | ||||||
| chr1:1284145
|
G | T | 1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.464+55G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284145 | ||||||
| chr1:1284146
|
G | T | 15 | a0001c0001t0001g0252a0001c0001t0002g0161a0001c0001t0002g0163others(12): Show | 15 | HG00558.hp1 HG01346.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.464+56G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284146 | ||||||
| chr1:1284147
|
G | GT | 9 | a0001c0036t0006g0123a0002c0003t0002g0032a0004c0005t0006g0128others(6): Show | 9 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.464+57_464+58insT | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284147 | ||||||
| chr1:1284148
|
G | T | 1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.464+58G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284148 | ||||||
| chr1:1284153
|
G | A | 1 | a0010c0019t0003g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.464+63G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284153 | ||||||
| chr1:1284158
|
A | G | 14 | a0001c0001t0001g0219a0001c0036t0006g0123a0002c0003t0001g0097others(11): Show | 14 | HG01993.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.464+68A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284158 | ||||||
| chr1:1284165
|
G | GGTCGGGG others(1688): Show |
1 | a0010c0035t0009g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.464+76_464+77insTC others(1693): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284165 | |||||
| chr1:1284167
|
G | A | 1 | a0010c0035t0009g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.464+77G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284167 | ||||||
| chr1:1284167
|
G | GGGTGGGG others(383): Show |
1 | a0003c0004t0003g0133 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.464+78_464+79insGT others(388): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284167 | |||||
| chr1:1284167
|
G | GGGTGGGG others(214): Show |
1 | a0003c0004t0003g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.464+78_464+79insGT others(219): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284167 | |||||
| chr1:1284167
|
G | GGGTGGGG others(1509): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.464+78_464+79insGT others(1514): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284167 | |||||
| chr1:1284167
|
G | GTGGGGGG others(255): Show |
1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.464+77_464+78insTG others(260): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284167 | ||||||
| chr1:1284169
|
T | G | 1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.464+79T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284169 | ||||||
| chr1:1284170
|
G | GGGGGGGT others(292): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(297): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284170 | |||||
| chr1:1284170
|
G | GGGGGGGT others(970): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(975): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284170 | |||||
| chr1:1284171
|
G | A | 4 | a0001c0001t0002g0173a0003c0004t0003g0133a0003c0004t0003g0137others(1): Show | 4 | HG01993.hp2 HG02723.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+81G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284171 | ||||||
| chr1:1284171
|
G | GGGGCGTT others(162): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.464+84_464+85insCG others(167): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGGT others(290): Show |
1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.464+86_464+87insGT others(295): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(326): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(331): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(456): Show |
1 | a0006c0010t0007g0270 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(461): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(348): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(353): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(1413): Show |
1 | a0024c0033t0009g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(1418): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(415): Show |
1 | a0002c0003t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(420): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(147): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(262): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(267): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(339): Show |
2 | a0002c0002t0001g0109a0002c0003t0001g0044 | 2 | HG00544.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(344): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(848): Show |
1 | a0002c0002t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(853): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(273): Show |
1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(278): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(239): Show |
1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(244): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(485): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(490): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(221): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(226): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(228): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(233): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(420): Show |
1 | a0014c0021t0008g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(425): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(261): Show |
1 | a0014c0021t0008g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(266): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(406): Show |
1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(411): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(964): Show |
1 | a0012c0022t0006g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(969): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(566): Show |
1 | a0006c0010t0007g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(571): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(293): Show |
1 | a0006c0015t0008g0276 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(298): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(292): Show |
1 | a0006c0015t0008g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(297): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(905): Show |
1 | a0006c0010t0007g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(910): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(501): Show |
1 | a0003c0004t0003g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(506): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(361): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(366): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(230): Show |
1 | a0008c0007t0004g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(235): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(564): Show |
1 | a0003c0004t0003g0145 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(569): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(61): Show |
1 | a0023c0045t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(66): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(495): Show |
1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(500): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(213): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(218): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(84): Show |
1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(89): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(425): Show |
1 | a0001c0001t0001g0178 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(430): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(327): Show |
1 | a0003c0004t0003g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(332): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(290): Show |
1 | a0027c0039t0002g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(295): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(371): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(376): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(211): Show |
15 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0187others(12): Show | 15 | HG00099.hp1 HG01106.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(216): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(492): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(497): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(564): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(569): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(561): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(566): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(381): Show |
1 | a0003c0004t0003g0151 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(386): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(290): Show |
1 | a0003c0004t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(295): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(299): Show |
3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02683.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(304): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(289): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(294): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(379): Show |
3 | a0003c0004t0003g0135a0003c0004t0003g0153a0022c0040t0012g0159 | 3 | NA18964.hp2 NA18998.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(384): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(189): Show |
4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(201): Show |
2 | a0003c0004t0003g0141a0003c0004t0003g0148 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(206): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(296): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(301): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(230): Show |
1 | a0003c0004t0003g0152 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(235): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(211): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(216): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(184): Show |
1 | a0001c0001t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(189): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(326): Show |
1 | a0003c0004t0003g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(331): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(323): Show |
1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(328): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(381): Show |
1 | a0003c0004t0003g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(386): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(649): Show |
1 | a0001c0001t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(654): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(838): Show |
1 | a0011c0023t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(843): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(838): Show |
2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(843): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(614): Show |
2 | a0004c0008t0001g0239a0004c0008t0001g0240 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(619): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(504): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(509): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(1386): Show |
1 | a0004c0008t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(1391): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(675): Show |
1 | a0001c0001t0001g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(680): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(558): Show |
2 | a0001c0001t0001g0244a0004c0008t0001g0262 | 2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(563): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(696): Show |
1 | a0001c0001t0001g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(701): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(607): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(612): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(613): Show |
1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(618): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(150): Show |
1 | a0003c0004t0003g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(155): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(304): Show |
1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(309): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(233): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(238): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(206): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(211): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(353): Show |
1 | a0011c0023t0001g0265 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(358): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(185): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(190): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(301): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(306): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGGTT others(1210): Show |
1 | a0003c0034t0009g0279 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTT others(1215): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGTTG others(96): Show |
1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464+85_464+86insTT others(101): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGTTG others(659): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.464+85_464+86insTT others(664): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGGTTG others(310): Show |
1 | a0004c0005t0006g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.464+85_464+86insTT others(315): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGGTTGG others(182): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.464+84_464+85insTT others(187): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTCGGG others(301): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTC others(306): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTGGGG others(245): Show |
1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.464+83_464+84insTG others(250): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTGTTG others(1769): Show |
1 | a0001c0001t0002g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTG others(1774): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTGTTG others(817): Show |
1 | a0001c0001t0001g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTG others(822): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTGTTG others(23): Show |
2 | a0001c0012t0001g0127a0001c0012t0001g0131 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.464+83_464+84insTG others(28): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTTGGG others(240): Show |
2 | a0001c0009t0001g0210a0001c0009t0001g0211 | 2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.464+83_464+84insTT others(245): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTTGGG others(190): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.464+83_464+84insTT others(195): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTTGGG others(189): Show |
4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG00741.hp2 HG01517.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+83_464+84insTT others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTTGGG others(277): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.464+83_464+84insTT others(282): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGGTTGGG others(316): Show |
1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTT others(321): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGTGAGGG others(299): Show |
1 | a0005c0011t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464+82_464+83insTG others(304): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284171
|
G | GGTGAGGG others(184): Show |
2 | a0005c0011t0001g0157a0005c0011t0001g0158 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.464+82_464+83insTG others(189): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284171 | |||||
| chr1:1284172
|
G | GGTGTTGG others(4): Show |
1 | a0001c0012t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.464+83_464+84insTG others(9): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284172 | |||||
| chr1:1284172
|
G | GGTGTTGG others(2189): Show |
1 | a0001c0001t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTG others(2194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284172 | |||||
| chr1:1284172
|
G | GGTGTTGG others(887): Show |
1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.464+83_464+84insTG others(892): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284172 | |||||
| chr1:1284173
|
G | GGGGGTTG others(301): Show |
1 | a0002c0002t0001g0037 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.464+86_464+87insGT others(306): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284173 | |||||
| chr1:1284173
|
G | GGGGGTTG others(329): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.464+86_464+87insGT others(334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284173 | |||||
| chr1:1284173
|
G | GGGTTGAG others(189): Show |
1 | a0004c0005t0010g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.464+85_464+86insTT others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284173 | |||||
| chr1:1284173
|
G | GGGTTGAG others(211): Show |
1 | a0004c0005t0010g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.464+85_464+86insTT others(216): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284173 | |||||
| chr1:1284173
|
G | GGGTTGGG others(1017): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.464+85_464+86insTT others(1022): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284173 | |||||
| chr1:1284173
|
G | GTCGGGGG others(154): Show |
1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTC others(159): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284173 | ||||||
| chr1:1284173
|
G | GTGGGGGG others(300): Show |
1 | a0003c0004t0003g0007 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTG others(305): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284173 | ||||||
| chr1:1284173
|
G | GTGTTGGG others(189): Show |
1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTG others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284173 | ||||||
| chr1:1284173
|
G | GTGTTGGG others(165): Show |
1 | a0013c0042t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.464+83_464+84insTG others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284173 | ||||||
| chr1:1284173
|
G | GTGTTGGG others(289): Show |
1 | a0010c0019t0003g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.464+83_464+84insTG others(294): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284173 | ||||||
| chr1:1284173
|
G | T | 1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.464+83G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284173 | ||||||
| chr1:1284177
|
T | G | 15 | a0001c0001t0001g0209a0001c0001t0001g0222a0001c0001t0002g0260others(12): Show | 15 | HG01106.hp2 HG01192.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.464+87T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284177 | ||||||
| chr1:1284177
|
T | TTGGGGTG others(128): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.464+92_464+93insTG others(133): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(34): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(39): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(125): Show |
1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(33): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(364): Show |
1 | a0009c0013t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(369): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(495): Show |
1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(500): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(247): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(252): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(125): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(216): Show |
1 | a0002c0028t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(221): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(124): Show |
28 | a0002c0002t0001g0008a0002c0002t0001g0019a0002c0002t0001g0023others(25): Show | 28 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(129): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(607): Show |
1 | a0002c0002t0001g0042 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(612): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(176): Show |
8 | a0002c0003t0004g0113a0002c0003t0004g0114a0002c0003t0004g0115others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(181): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(267): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(272): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(215): Show |
1 | a0002c0002t0001g0017 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(220): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(811): Show |
1 | a0002c0002t0001g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(816): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(212): Show |
1 | a0002c0002t0001g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(217): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(265): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(270): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(104): Show |
1 | a0002c0002t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(109): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(124): Show |
1 | a0002c0002t0001g0010 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(129): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(121): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(72): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(77): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(331): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(336): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(243): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(248): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(263): Show |
2 | a0002c0002t0001g0065a0002c0002t0001g0066 | 2 | HG02165.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(268): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(262): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(267): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(241): Show |
1 | a0002c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(246): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(241): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(246): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(111): Show |
3 | a0007c0006t0001g0072a0007c0006t0001g0073a0007c0006t0001g0100 | 3 | HG02451.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(122): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(127): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(376): Show |
1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(381): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(177): Show |
1 | a0002c0002t0013g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(182): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(85): Show |
1 | a0002c0002t0001g0076 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(177): Show |
1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(182): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(176): Show |
5 | a0002c0002t0001g0077a0002c0002t0001g0096a0002c0002t0001g0108others(2): Show | 5 | HG03704.hp2 NA18954.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(181): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(154): Show |
1 | a0002c0002t0001g0079 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(159): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(258): Show |
1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(263): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(205): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(210): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(206): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(211): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(199): Show |
1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(105): Show |
2 | a0002c0002t0001g0003a0002c0002t0001g0035 | 2 | HG00438.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(183): Show |
1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(188): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(175): Show |
5 | a0002c0003t0002g0015a0002c0003t0002g0081a0002c0003t0002g0082others(2): Show | 5 | HG02683.hp1 HG03017.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(180): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(328): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(333): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(116): Show |
1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(121): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(279): Show |
1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(284): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(129): Show |
1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(65): Show |
1 | a0002c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(70): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(193): Show |
1 | a0002c0002t0001g0086 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(198): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(262): Show |
1 | a0002c0002t0001g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(267): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(304): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(309): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(387): Show |
1 | a0001c0020t0001g0176 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(392): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(105): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(773): Show |
1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(778): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(266): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(271): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(316): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(321): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(1038): Show |
1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(1043): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(211): Show |
1 | a0001c0001t0001g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(216): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(251): Show |
1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(256): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(389): Show |
1 | a0001c0001t0001g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(394): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(535): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(540): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(329): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(376): Show |
1 | a0001c0001t0005g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(381): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(416): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(421): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(328): Show |
5 | a0001c0001t0002g0169a0001c0001t0002g0228a0001c0001t0002g0229others(2): Show | 5 | HG00408.hp1 HG01928.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(333): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(468): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(473): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(540): Show |
1 | a0001c0001t0002g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(545): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(495): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(500): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(345): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(350): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(394): Show |
1 | a0001c0001t0005g0235 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(399): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(666): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(671): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGA others(131): Show |
1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(136): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(648): Show |
1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(653): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(363): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(368): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(362): Show |
1 | a0001c0001t0002g0249 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(367): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(450): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(455): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(408): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(413): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(360): Show |
1 | a0001c0001t0002g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(365): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(333): Show |
3 | a0003c0004t0003g0004a0003c0004t0003g0005a0003c0004t0003g0253 | 3 | NA19007.hp2 NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.464+91_464+92insTG others(338): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(155): Show |
4 | a0003c0004t0003g0006a0003c0004t0003g0171a0003c0004t0003g0172others(1): Show | 4 | HG01346.hp1 HG02155.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+91_464+92insTG others(160): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(475): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(480): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(474): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(479): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(280): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(285): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284177
|
T | TTGGGTGG others(288): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(293): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284177 | |||||
| chr1:1284178
|
T | TGGGTGAG others(126): Show |
1 | a0002c0002t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(131): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284178 | |||||
| chr1:1284178
|
T | TGGGTGAG others(214): Show |
1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(219): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284178 | |||||
| chr1:1284179
|
G | GGGTGAGG others(124): Show |
1 | a0016c0031t0001g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(129): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284179 | |||||
| chr1:1284179
|
G | GGGTGAGG others(338): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(343): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284179 | |||||
| chr1:1284179
|
G | GGGTGAGG others(530): Show |
1 | a0002c0002t0001g0030 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(535): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284179 | |||||
| chr1:1284179
|
G | GGGTGAGG others(260): Show |
1 | a0003c0004t0003g0146 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(265): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284179 | |||||
| chr1:1284179
|
G | GGGTGGGG others(830): Show |
1 | a0001c0001t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.464+91_464+92insTG others(835): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284179 | |||||
| chr1:1284179
|
G | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0222 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.464+89G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284179 | ||||||
| chr1:1284181
|
G | GTGAGGGG others(294): Show |
1 | a0002c0002t0001g0067 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.464+91_464+92insTG others(299): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284181 | ||||||
| chr1:1284184
|
G | T | 1 | a0002c0002t0001g0030 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.464+94G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284184 | ||||||
| chr1:1284186
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.464+96T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284186 | ||||||
| chr1:1284189
|
G | A | 8 | a0001c0001t0011g0268a0001c0020t0001g0176a0001c0047t0001g0183others(5): Show | 8 | HG00099.hp2 HG01169.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.464+99G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284189 | ||||||
| chr1:1284189
|
G | GGTGAGGG others(42): Show |
1 | a0001c0012t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.464+108_464+109ins others(49): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284189 | |||||
| chr1:1284189
|
G | GGTGAGGG others(80): Show |
2 | a0001c0012t0001g0127a0001c0012t0001g0131 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.464+108_464+109ins others(87): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284189 | |||||
| chr1:1284190
|
G | A | 1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.464+100G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284190 | ||||||
| chr1:1284199
|
T | G | 3 | a0002c0002t0001g0067a0002c0002t0001g0076a0025c0044t0003g0257 | 3 | HG02559.hp2 NA18960.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.464+109T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284199 | ||||||
| chr1:1284203
|
G | GGGGTTGG others(11): Show |
1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.464+116_464+117ins others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284203 | |||||
| chr1:1284212
|
A | G | 8 | a0001c0001t0011g0268a0001c0020t0001g0176a0002c0002t0001g0067others(5): Show | 8 | HG01169.hp2 HG01243.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.464+122A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284212 | ||||||
| chr1:1284292
|
C | CGTGGGGG others(7): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.464+211_464+224dup others(14): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284292 | |||||
| chr1:1284308
|
T | G | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.464+218T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284308 | ||||||
| chr1:1284308
|
T | TG | 10 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0002g0140others(7): Show | 10 | HG00544.hp2 HG00741.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.464+224dupG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284308 | |||||
| chr1:1284309
|
G | T | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.464+219G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284309 | ||||||
| chr1:1284316
|
A | AGGGGTGG others(1): Show |
13 | a0005c0011t0001g0157a0005c0011t0001g0158a0005c0016t0001g0281others(10): Show | 13 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.464+236_464+243dup others(8): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284316 | |||||
| chr1:1284321
|
T | TG | 12 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0011g0267others(9): Show | 12 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.464+238dupG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284321 | |||||
| chr1:1284383
|
CTCTTTCC others(31): Show |
C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.464+294_464+331del others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284383 | ||||||
| chr1:1284395
|
C | T | 19 | a0002c0002t0001g0025a0002c0002t0001g0059a0003c0004t0003g0004others(16): Show | 19 | HG00597.hp2 HG00738.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.464+305C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284395 | ||||||
| chr1:1284529
|
G | A | 1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.464+439G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284529 | ||||||
| chr1:1284529
|
GAGCGTGT others(21): Show |
G | 2 | a0003c0004t0003g0171a0003c0004t0003g0172 | 2 | HG02165.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.464+466_464+493del others(28): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284529 | |||||
| chr1:1284551
|
G | T | 11 | a0003c0034t0009g0279a0006c0010t0007g0270a0006c0010t0007g0273others(8): Show | 11 | HG00597.hp2 HG00738.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.464+461G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284551 | ||||||
| chr1:1284557
|
C | CAGCGTGT others(21): Show |
1 | a0003c0004t0003g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.464+513_464+540dup others(28): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284557 | |||||
| chr1:1284557
|
CAGCGTGT others(21): Show |
C | 1 | a0004c0005t0006g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.464+513_464+540del others(28): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284557 | |||||
| chr1:1284561
|
G | A | 40 | a0001c0001t0001g0162a0001c0001t0001g0209a0001c0001t0001g0222others(37): Show | 40 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.464+471G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284561 | ||||||
| chr1:1284561
|
G | GTGTGCTG others(49): Show |
6 | a0002c0003t0001g0063a0002c0003t0002g0032a0002c0003t0002g0038others(3): Show | 6 | NA18946.hp1 NA18971.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.464+512_464+513ins others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284561 | |||||
| chr1:1284574
|
C | CG | 15 | a0001c0001t0001g0167a0001c0001t0001g0187a0001c0001t0001g0200others(12): Show | 15 | HG00558.hp1 HG00738.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.464+490dupG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284574 | |||||
| chr1:1284574
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.464+484C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284574 | ||||||
| chr1:1284585
|
G | A | 1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.464+495G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284585 | ||||||
| chr1:1284602
|
C | CG | 11 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0046t0001g0259others(8): Show | 11 | HG00544.hp2 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.464+518dupG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284602 | |||||
| chr1:1284629
|
A | C | 1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.464+539A>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284629 | ||||||
| chr1:1284636
|
G | T | 1 | a0002c0003t0002g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.464+546G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284636 | ||||||
| chr1:1284639
|
CACAGTGT others(15): Show |
C | 1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.464+550_464+571del others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284639 | ||||||
| chr1:1284726
|
G | A | 4 | a0003c0004t0003g0133a0003c0004t0003g0135a0003c0004t0003g0153others(1): Show | 4 | NA18964.hp2 NA18998.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+636G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284726 | ||||||
| chr1:1284756
|
A | G | 154 | a0001c0001t0001g0209a0001c0001t0001g0222a0001c0001t0001g0223others(151): Show | 154 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.464+666A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284756 | ||||||
| chr1:1284786
|
T | C | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.464+696T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284786 | ||||||
| chr1:1284808
|
G | A | 1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.464+718G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284808 | ||||||
| chr1:1284814
|
A | G | 3 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158 | 3 | HG02622.hp2 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.464+724A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284814 | ||||||
| chr1:1284822
|
T | G | 1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.464+732T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284822 | ||||||
| chr1:1284826
|
G | A | 1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.464+736G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284826 | ||||||
| chr1:1284843
|
C | G | 9 | a0005c0016t0001g0281a0005c0016t0001g0289a0005c0017t0001g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.465-728C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284843 | ||||||
| chr1:1284938
|
GCCCCCAC others(30): Show |
G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-631_465-595del others(37): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1284938 | |||||
| chr1:1284950
|
G | A | 1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.465-621G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284950 | ||||||
| chr1:1284976
|
C | A | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-595C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284976 | ||||||
| chr1:1284979
|
G | C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-592G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284979 | ||||||
| chr1:1284980
|
T | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-591T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284980 | ||||||
| chr1:1284985
|
A | C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-586A>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284985 | ||||||
| chr1:1284986
|
C | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-585C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284986 | ||||||
| chr1:1284987
|
G | A | 6 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(3): Show | 6 | HG00642.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.465-584G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284987 | ||||||
| chr1:1284988
|
A | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-583A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284988 | ||||||
| chr1:1284992
|
G | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-579G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284992 | ||||||
| chr1:1284998
|
A | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-573A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1284998 | ||||||
| chr1:1285005
|
T | C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-566T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285005 | ||||||
| chr1:1285010
|
A | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-561A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285010 | ||||||
| chr1:1285011
|
A | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-560A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285011 | ||||||
| chr1:1285013
|
A | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-558A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285013 | ||||||
| chr1:1285020
|
C | A | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-551C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285020 | ||||||
| chr1:1285022
|
A | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-549A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285022 | ||||||
| chr1:1285025
|
C | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-546C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285025 | ||||||
| chr1:1285029
|
T | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-542T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285029 | ||||||
| chr1:1285042
|
C | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-529C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285042 | ||||||
| chr1:1285045
|
A | G | 22 | a0002c0002t0001g0023a0002c0003t0002g0012a0002c0003t0002g0021others(19): Show | 22 | HG00597.hp2 HG00738.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.465-526A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285045 | ||||||
| chr1:1285046
|
T | G | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-525T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285046 | ||||||
| chr1:1285059
|
G | C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-512G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285059 | ||||||
| chr1:1285061
|
A | C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-510A>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285061 | ||||||
| chr1:1285062
|
G | T | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-509G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285062 | ||||||
| chr1:1285066
|
G | C | 1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-505G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285066 | ||||||
| chr1:1285072
|
A | AGGAGCCG others(76): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.465-498_465-497ins others(83): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1285072 | |||||
| chr1:1285124
|
G | A | 102 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(99): Show | 102 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.465-447G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285124 | ||||||
| chr1:1285125
|
G | C | 1 | a0016c0031t0001g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.465-446G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285125 | ||||||
| chr1:1285135
|
C | A | 1 | a0003c0004t0003g0133 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.465-436C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285135 | ||||||
| chr1:1285173
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465-398G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285173 | ||||||
| chr1:1285230
|
C | T | 7 | a0001c0036t0006g0123a0004c0005t0006g0126a0004c0005t0006g0128others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.465-341C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285230 | ||||||
| chr1:1285287
|
C | CG | 4 | a0001c0001t0001g0209a0002c0003t0002g0024a0006c0010t0007g0273others(1): Show | 4 | HG00597.hp2 HG00642.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.465-281dupG | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 1285287 | |||||
| chr1:1285385
|
C | T | 9 | a0005c0016t0001g0281a0005c0016t0001g0289a0005c0017t0001g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.465-186C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285385 | ||||||
| chr1:1285405
|
C | T | 1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.465-166C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285405 | ||||||
| chr1:1285442
|
G | A | 9 | a0005c0016t0001g0281a0005c0016t0001g0289a0005c0017t0001g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.465-129G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 5/17 | chr1 | 1285442 | ||||||
| chr1:1285674
|
G | T | 2 | a0012c0022t0006g0132a0012c0022t0006g0269 | 2 | HG00642.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.558+10G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285674 | ||||||
| chr1:1285675
|
A | G | 2 | a0012c0022t0006g0132a0012c0022t0006g0269 | 2 | HG00642.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.558+11A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285675 | ||||||
| chr1:1285758
|
G | A | 115 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(112): Show | 115 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.558+94G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285758 | ||||||
| chr1:1285767
|
C | G | 3 | a0002c0003t0004g0118a0002c0003t0004g0119a0002c0003t0004g0120 | 3 | HG01884.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.558+103C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285767 | ||||||
| chr1:1285784
|
T | C | 2 | a0014c0021t0008g0271a0014c0021t0008g0272 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.558+120T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285784 | ||||||
| chr1:1285817
|
G | A | 6 | a0002c0003t0001g0063a0002c0003t0002g0032a0002c0003t0002g0038others(3): Show | 6 | NA18946.hp1 NA18971.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.559-109G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285817 | ||||||
| chr1:1285896
|
C | T | 6 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(3): Show | 6 | HG01069.hp1 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-30C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285896 | ||||||
| chr1:1285922
|
A | G | 6 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(3): Show | 6 | HG00642.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.559-4A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 6/17 | chr1 | 1285922 | ||||||
| chr1:1286299
|
C | T | 1 | a0013c0042t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.911+21C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286299 | ||||||
| chr1:1286312
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.911+34C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286312 | ||||||
| chr1:1286337
|
C | T | 115 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(112): Show | 115 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.911+59C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286337 | ||||||
| chr1:1286348
|
G | A | 9 | a0005c0016t0001g0281a0005c0016t0001g0289a0005c0017t0001g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.911+70G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286348 | ||||||
| chr1:1286430
|
T | G | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.911+152T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286430 | ||||||
| chr1:1286432
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.911+154G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286432 | ||||||
| chr1:1286532
|
T | C | 13 | a0001c0036t0006g0123a0004c0005t0006g0126a0004c0005t0006g0128others(10): Show | 13 | HG00642.hp1 HG01243.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.912-236T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286532 | ||||||
| chr1:1286579
|
C | T | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.912-189C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286579 | ||||||
| chr1:1286591
|
G | C | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.912-177G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286591 | ||||||
| chr1:1286592
|
C | A | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.912-176C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286592 | ||||||
| chr1:1286671
|
A | G | 15 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(12): Show | 15 | HG00642.hp1 HG01069.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.912-97A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286671 | ||||||
| chr1:1286671
|
A | T | 7 | a0001c0036t0006g0123a0004c0005t0006g0126a0004c0005t0006g0128others(4): Show | 7 | HG01243.hp2 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.912-97A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 7/17 | chr1 | 1286671 | ||||||
| chr1:1287027
|
C | T | 4 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+52C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 8/17 | chr1 | 1287027 | ||||||
| chr1:1287053
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1120-56T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 8/17 | chr1 | 1287053 | ||||||
| chr1:1287310
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0199others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1310+11C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | chr1 | 1287310 | ||||||
| chr1:1287315
|
G | C | 124 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(121): Show | 124 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1310+16G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | chr1 | 1287315 | ||||||
| chr1:1287359
|
C | G | 16 | a0002c0002t0001g0084a0002c0003t0001g0026a0002c0003t0001g0063others(13): Show | 16 | HG00597.hp1 HG01243.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1310+60C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | chr1 | 1287359 | ||||||
| chr1:1287365
|
G | A | 1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1310+66G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | chr1 | 1287365 | ||||||
| chr1:1287406
|
G | GAGGAACT others(11): Show |
1 | a0002c0002t0001g0008 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1311-101_1311-84du others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 1287406 | |||||
| chr1:1287415
|
T | C | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1311-93T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | chr1 | 1287415 | ||||||
| chr1:1287416
|
C | T | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1311-92C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 9/17 | chr1 | 1287416 | ||||||
| chr1:1287599
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | splice_region_variant&intron_variant | LOW | c.1399+3G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 10/17 | chr1 | 1287599 | ||||||
| chr1:1287863
|
C | T | 2 | a0003c0004t0003g0145a0003c0004t0003g0151 | 2 | HG03490.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1563+27C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 11/17 | chr1 | 1287863 | ||||||
| chr1:1287868
|
C | T | 2 | a0001c0036t0006g0123a0004c0005t0006g0128 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1563+32C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 11/17 | chr1 | 1287868 | ||||||
| chr1:1287895
|
G | C | 2 | a0001c0001t0001g0245a0001c0020t0001g0263 | 2 | HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1564-44G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 11/17 | chr1 | 1287895 | ||||||
| chr1:1287934
|
C | T | 1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | splice_region_variant&intron_variant | LOW | c.1564-5C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 11/17 | chr1 | 1287934 | ||||||
| chr1:1288024
|
C | CCTACACC others(12): Show |
1 | a0020c0030t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1652_1662+8dupACAC others(15): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288024 | |||||
| chr1:1288032
|
AGGCAGGT others(26): Show |
A | 1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+17_1662+49del others(33): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288032 | |||||
| chr1:1288047
|
G | A | 10 | a0001c0001t0002g0169a0001c0001t0002g0173a0001c0001t0002g0228others(7): Show | 10 | HG00408.hp1 HG01928.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662+10G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288047 | ||||||
| chr1:1288049
|
C | T | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+12C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288049 | ||||||
| chr1:1288062
|
C | T | 3 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158 | 3 | HG02622.hp2 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1662+25C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288062 | ||||||
| chr1:1288085
|
GC | G | 66 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0188others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1662+50delC | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288085 | |||||
| chr1:1288086
|
C | CAGGGGGT others(25): Show |
3 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158 | 3 | HG02622.hp2 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1662+49_1662+50ins others(32): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288086 | ||||||
| chr1:1288149
|
G | C | 32 | a0002c0002t0001g0011a0002c0002t0001g0013a0002c0002t0001g0016others(29): Show | 32 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1662+112G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288149 | ||||||
| chr1:1288160
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1662+123C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288160 | ||||||
| chr1:1288170
|
C | T | 1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+133C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288170 | ||||||
| chr1:1288190
|
C | CCCGCTCC others(31): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1662+177_1662+178i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288190 | |||||
| chr1:1288190
|
C | T | 4 | a0004c0005t0010g0124a0004c0005t0010g0125a0010c0035t0009g0280others(1): Show | 4 | HG02723.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+153C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288190 | ||||||
| chr1:1288192
|
C | T | 4 | a0004c0005t0010g0124a0004c0005t0010g0125a0010c0035t0009g0280others(1): Show | 4 | HG02723.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+155C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288192 | ||||||
| chr1:1288200
|
TCCCTGTG others(140): Show |
T | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1662+167_1662+313d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288200 | |||||
| chr1:1288204
|
T | C | 11 | a0001c0012t0001g0127a0001c0012t0001g0130a0001c0012t0001g0131others(8): Show | 11 | HG01243.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+167T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288204 | ||||||
| chr1:1288204
|
T | TGTGTCCC others(29): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1662+172_1662+173i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
T | TGTGTCTC others(85): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+177_1662+178i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
T | TGTGTCTC others(173): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1662+177_1662+178i others(182): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
T | TGTGTCTC others(47): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1662+190_1662+191i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
T | TGTGTCTC others(65): Show |
2 | a0002c0002t0001g0029a0017c0029t0001g0048 | 2 | HG00423.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1662+190_1662+191i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
T | TGTGTCTC others(157): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+190_1662+191i others(166): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
TGTGTCTC others(11): Show |
T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1662+222_1662+239d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288204
|
TGTGTCTC others(139): Show |
T | 5 | a0002c0002t0001g0025a0002c0002t0001g0037a0002c0002t0001g0052others(2): Show | 5 | HG00544.hp1 HG03704.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+191_1662+336d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288204 | |||||
| chr1:1288206
|
TGTCTCTG others(67): Show |
T | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1662+192_1662+265d others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288206 | |||||
| chr1:1288209
|
C | CTCTGCCC others(9): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+177_1662+178i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288209 | |||||
| chr1:1288210
|
T | TCTGCTCC others(11): Show |
1 | a0002c0002t0001g0042 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1662+190_1662+191i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288210 | |||||
| chr1:1288210
|
T | TCTGCTCC others(29): Show |
2 | a0002c0002t0001g0030a0002c0003t0002g0081 | 2 | HG03688.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1662+190_1662+191i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288210 | |||||
| chr1:1288210
|
TCTGCTCC others(175): Show |
T | 4 | a0002c0002t0001g0047a0002c0002t0001g0057a0002c0002t0001g0062others(1): Show | 4 | HG00673.hp1 HG01952.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+191_1662+372d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288210 | |||||
| chr1:1288210
|
TCTGCTCC others(193): Show |
T | 1 | a0002c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1662+191_1662+390d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288210 | |||||
| chr1:1288210
|
TCTGCTCC others(303): Show |
T | 1 | a0003c0034t0009g0279 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1662+204_1662+513d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288210 | |||||
| chr1:1288215
|
T | C | 30 | a0001c0001t0001g0165a0001c0001t0001g0222a0001c0001t0001g0223others(27): Show | 30 | HG00558.hp2 HG01106.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1662+178T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288215 | ||||||
| chr1:1288215
|
T | TCCGTCCC others(83): Show |
3 | a0002c0002t0001g0034a0002c0002t0001g0094a0015c0037t0001g0090 | 3 | HG01081.hp2 HG04184.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1662+190_1662+191i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288215 | |||||
| chr1:1288215
|
T | TCCGTCCC others(83): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1662+190_1662+191i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288215 | |||||
| chr1:1288219
|
T | TCCCGTGT others(13): Show |
1 | a0013c0042t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1662+190_1662+191i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288219 | |||||
| chr1:1288219
|
T | TCCCGTGT others(363): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1662+231_1662+232i others(372): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288219 | |||||
| chr1:1288219
|
T | TCCCGTGT others(269): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1662+231_1662+232i others(278): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288219 | |||||
| chr1:1288221
|
CCG | C | 12 | a0001c0001t0001g0222a0001c0001t0001g0223a0003c0004t0003g0141others(9): Show | 12 | HG00558.hp2 HG01106.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1662+185_1662+186d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288221 | ||||||
| chr1:1288221
|
CCGTGTCT others(13): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1662+185_1662+204d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288221 | ||||||
| chr1:1288221
|
CCGTGTCT others(603): Show |
C | 1 | a0012c0022t0006g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1662+186_1662+795d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288221 | |||||
| chr1:1288222
|
C | CCT | 3 | a0001c0036t0006g0123a0004c0005t0010g0124a0004c0005t0010g0125 | 3 | HG03209.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+185_1662+186i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288222 | ||||||
| chr1:1288222
|
C | CGTGTCTC others(13): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1662+198_1662+199i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288222 | |||||
| chr1:1288222
|
C | T | 10 | a0002c0002t0001g0079a0003c0004t0003g0133a0003c0004t0003g0134others(7): Show | 10 | HG02155.hp2 HG03490.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662+185C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288222 | ||||||
| chr1:1288226
|
TCTCTGCT others(141): Show |
T | 4 | a0003c0004t0003g0133a0003c0004t0003g0135a0003c0004t0003g0137others(1): Show | 4 | NA18964.hp2 NA18998.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+192_1662+339d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288226 | |||||
| chr1:1288226
|
TCTCTGCT others(159): Show |
T | 1 | a0002c0002t0001g0079 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1662+192_1662+357d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288226 | |||||
| chr1:1288227
|
C | CTGCTCCG others(25): Show |
5 | a0003c0004t0003g0134a0003c0004t0003g0144a0003c0004t0003g0145others(2): Show | 5 | HG03490.hp1 NA18967.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+191_1662+192i others(34): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288227 | |||||
| chr1:1288227
|
C | G | 12 | a0001c0001t0001g0222a0001c0001t0001g0223a0003c0004t0003g0141others(9): Show | 12 | HG00558.hp2 HG01106.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1662+190C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288227 | ||||||
| chr1:1288227
|
CTCTGCTC others(65): Show |
C | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1662+209_1662+280d others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288227 | |||||
| chr1:1288228
|
T | C | 61 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0010others(58): Show | 61 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1662+191T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288228 | ||||||
| chr1:1288228
|
T | TCTGCTCC others(11): Show |
2 | a0001c0047t0001g0183a0002c0003t0002g0015 | 2 | HG00099.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1662+208_1662+209i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288228 | |||||
| chr1:1288228
|
T | TCTGCTCC others(117): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1662+209_1662+210i others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288228 | |||||
| chr1:1288228
|
TCTGCTCC others(139): Show |
T | 3 | a0003c0004t0003g0005a0003c0004t0003g0006a0003c0004t0003g0253 | 3 | HG01346.hp1 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1662+209_1662+354d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288228 | |||||
| chr1:1288228
|
TCTGCTCC others(175): Show |
T | 1 | a0003c0004t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1662+209_1662+390d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288228 | |||||
| chr1:1288233
|
T | C | 8 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0245others(5): Show | 8 | HG00423.hp1 HG01891.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+196T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288233 | ||||||
| chr1:1288233
|
T | TCCGTCCC others(11): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1662+213_1662+214i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288233 | |||||
| chr1:1288233
|
T | TCCGTCCC others(31): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1662+221_1662+222i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288233 | |||||
| chr1:1288233
|
TCCGTCCC others(101): Show |
T | 1 | a0009c0013t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1662+204_1662+311d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288233 | |||||
| chr1:1288236
|
G | A | 5 | a0007c0006t0001g0072a0008c0007t0004g0266a0008c0007t0004g0285others(2): Show | 5 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+199G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288236 | ||||||
| chr1:1288237
|
T | TCCCGTGT others(175): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1662+213_1662+214i others(184): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288237 | |||||
| chr1:1288237
|
T | TTC | 5 | a0007c0006t0001g0072a0008c0007t0004g0266a0008c0007t0004g0285others(2): Show | 5 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+200_1662+201i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288237 | ||||||
| chr1:1288237
|
TCCCGTGT others(103): Show |
T | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662+227_1662+336d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288237 | |||||
| chr1:1288239
|
CCGTGTCT others(81): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1662+204_1662+291d others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288239 | |||||
| chr1:1288240
|
C | CGTGTCCC others(31): Show |
5 | a0001c0001t0001g0252a0001c0018t0001g0251a0003c0004t0003g0171others(2): Show | 5 | HG02071.hp1 HG02155.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+208_1662+209i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288240 | |||||
| chr1:1288240
|
C | CGTGTCTC others(65): Show |
19 | a0001c0001t0001g0162a0001c0001t0002g0140a0001c0001t0002g0161others(16): Show | 19 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1662+227_1662+228i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288240 | |||||
| chr1:1288240
|
C | CGTGTCTC others(193): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1662+227_1662+228i others(202): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288240 | |||||
| chr1:1288240
|
C | T | 4 | a0008c0007t0004g0266a0008c0007t0004g0285a0008c0007t0004g0286others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+203C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288240 | ||||||
| chr1:1288242
|
TGTCTCTG others(31): Show |
T | 2 | a0003c0004t0003g0148a0003c0004t0003g0151 | 2 | HG02896.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1662+228_1662+265d others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288242 | |||||
| chr1:1288245
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1662+208C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288245 | ||||||
| chr1:1288246
|
T | C | 76 | a0001c0001t0001g0199a0001c0001t0005g0235a0002c0002t0001g0003others(73): Show | 76 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1662+209T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288246 | ||||||
| chr1:1288246
|
T | TCTGCTCC others(177): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+231_1662+232i others(186): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288246 | |||||
| chr1:1288246
|
TCTGCTCC others(1073): Show |
T | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1662+222_1663-933d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288246 | |||||
| chr1:1288248
|
T | C | 1 | a0016c0031t0001g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1662+211T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288248 | ||||||
| chr1:1288251
|
T | C | 13 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0250others(10): Show | 13 | HG01109.hp1 HG01934.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662+214T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288251 | ||||||
| chr1:1288251
|
TCCGTCCC others(383): Show |
T | 1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1662+240_1662+629d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288251 | |||||
| chr1:1288253
|
C | T | 3 | a0001c0020t0001g0176a0002c0002t0001g0109a0002c0003t0001g0044 | 3 | HG00544.hp2 HG01169.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1662+216C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288253 | ||||||
| chr1:1288254
|
G | A | 5 | a0001c0012t0001g0127a0001c0012t0001g0131a0004c0005t0010g0124others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+217G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288254 | ||||||
| chr1:1288255
|
T | TCC | 4 | a0001c0047t0001g0183a0006c0015t0008g0276a0006c0015t0008g0277others(1): Show | 4 | HG00099.hp2 NA18946.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+220_1662+221d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288255 | |||||
| chr1:1288255
|
T | TCCCCCGT others(51): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1662+221_1662+222i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288255 | |||||
| chr1:1288255
|
T | TCCCGTGT others(439): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1662+227_1662+228i others(448): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288255 | |||||
| chr1:1288255
|
T | TTC | 3 | a0004c0005t0010g0124a0004c0005t0010g0125a0016c0031t0001g0092 | 3 | HG03209.hp2 NA18522.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1662+218_1662+219i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288255 | ||||||
| chr1:1288255
|
TCCCGTGT others(85): Show |
T | 7 | a0002c0002t0001g0031a0002c0002t0001g0059a0002c0002t0001g0067others(4): Show | 7 | HG00621.hp2 HG03490.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662+240_1662+331d others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288255 | |||||
| chr1:1288255
|
TCCCGTGT others(195): Show |
T | 6 | a0002c0002t0001g0013a0002c0002t0001g0017a0002c0002t0001g0066others(3): Show | 6 | HG01361.hp1 HG01943.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+240_1662+441d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288255 | |||||
| chr1:1288255
|
TCCCGTGT others(1866): Show |
T | 2 | a0001c0001t0005g0235a0010c0035t0009g0280 | 2 | HG02723.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1662+240_1663-122d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288255 | |||||
| chr1:1288258
|
C | T | 3 | a0004c0005t0010g0124a0004c0005t0010g0125a0016c0031t0001g0092 | 3 | HG03209.hp2 NA18522.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1662+221C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288258 | ||||||
| chr1:1288260
|
T | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01106.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1662+223T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288260 | ||||||
| chr1:1288261
|
GTC | G | 10 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0248others(7): Show | 10 | HG00597.hp2 HG02074.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662+228_1662+229d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288261 | |||||
| chr1:1288261
|
GTCTCTGC others(30): Show |
G | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1662+225_1662+261d others(39): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288261 | ||||||
| chr1:1288261
|
GTCTCTGC others(87): Show |
G | 4 | a0006c0010t0007g0270a0006c0010t0007g0274a0006c0010t0007g0275others(1): Show | 4 | HG00738.hp1 HG01496.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+228_1662+321d others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288261 | |||||
| chr1:1288262
|
TCTCTGCT others(49): Show |
T | 4 | a0003c0004t0003g0141a0003c0004t0003g0142a0003c0004t0003g0143others(1): Show | 4 | HG00558.hp2 HG01109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+228_1662+283d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288262 | |||||
| chr1:1288263
|
CTCTGCTC others(29): Show |
C | 3 | a0002c0002t0001g0058a0004c0008t0001g0247a0013c0042t0001g0129 | 3 | HG03139.hp1 NA19005.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1662+240_1662+275d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288263 | |||||
| chr1:1288263
|
CTCTGCTC others(1702): Show |
C | 1 | a0001c0001t0001g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1662+240_1663-286d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288263 | |||||
| chr1:1288264
|
T | C | 10 | a0001c0012t0001g0130a0002c0002t0001g0011a0002c0002t0001g0033others(7): Show | 10 | HG00408.hp2 HG02300.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662+227T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288264 | ||||||
| chr1:1288264
|
TCTGCTCC others(47): Show |
T | 1 | a0008c0007t0004g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1662+240_1662+293d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288264
|
TCTGCTCC others(103): Show |
T | 3 | a0001c0001t0001g0242a0002c0002t0001g0042a0002c0002t0001g0085 | 3 | HG02922.hp2 NA18747.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1662+240_1662+349d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288264
|
TCTGCTCC others(157): Show |
T | 1 | a0004c0005t0006g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1662+240_1662+403d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288264
|
TCTGCTCC others(249): Show |
T | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1662+240_1662+495d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288264
|
TCTGCTCC others(1299): Show |
T | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1662+240_1663-689d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288264
|
TCTGCTCC others(1720): Show |
T | 1 | a0014c0021t0008g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1662+240_1663-268d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288264
|
TCTGCTCC others(1920): Show |
T | 1 | a0011c0023t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1662+240_1663-68de others(1): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288264 | |||||
| chr1:1288266
|
T | C | 4 | a0002c0003t0002g0101a0003c0004t0003g0004a0003c0004t0003g0007others(1): Show | 4 | HG02300.hp2 NA18961.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+229T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288266 | ||||||
| chr1:1288269
|
T | C | 32 | a0001c0001t0001g0243a0001c0001t0002g0233a0001c0012t0001g0127others(29): Show | 32 | HG01069.hp1 HG01081.hp2 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.1662+232T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288269 | ||||||
| chr1:1288269
|
TCCGTCCC others(365): Show |
T | 1 | a0002c0028t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1662+240_1662+611d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288269 | |||||
| chr1:1288272
|
G | A | 6 | a0002c0003t0002g0101a0003c0004t0003g0004a0003c0004t0003g0007others(3): Show | 6 | HG02300.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+235G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288272 | ||||||
| chr1:1288273
|
TCC | T | 58 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0243others(55): Show | 58 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1662+240_1662+241d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288273 | |||||
| chr1:1288273
|
TCCCCCGA others(67): Show |
T | 2 | a0002c0002t0001g0011a0009c0013t0001g0078 | 2 | NA19002.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1662+240_1662+313d others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288273 | |||||
| chr1:1288273
|
TCCCCCGA others(177): Show |
T | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1662+240_1662+423d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288273 | |||||
| chr1:1288273
|
TCCCCCGA others(289): Show |
T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0002c0002t0001g0010 | 3 | HG01106.hp2 HG01261.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1662+240_1662+535d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288273 | |||||
| chr1:1288274
|
C | CCCGTGTC others(29): Show |
1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288274 | |||||
| chr1:1288274
|
C | CCCGTGTC others(9): Show |
1 | a0027c0039t0002g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288274 | |||||
| chr1:1288274
|
C | T | 6 | a0002c0003t0002g0101a0003c0004t0003g0004a0003c0004t0003g0007others(3): Show | 6 | HG02300.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+237C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288274 | ||||||
| chr1:1288275
|
C | CCCCGTGT others(193): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1662+242_1662+243i others(202): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(27): Show |
1 | a0001c0012t0001g0131 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(363): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(372): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(9): Show |
15 | a0001c0009t0001g0218a0002c0002t0001g0008a0002c0002t0001g0019others(12): Show | 15 | HG01123.hp1 HG01169.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1662+239_1662+240i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(67): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(65): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(125): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(63): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(101): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(1015): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(1024): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(505): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(514): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(211): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(220): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(357): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(366): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(175): Show |
1 | a0002c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(184): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(752): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(761): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(101): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(119): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(128): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(139): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(139): Show |
1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(197): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(206): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(119): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(128): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(65): Show |
1 | a0002c0002t0001g0030 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1662+239_1662+240i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
C | CCGTGTCT others(379): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1662+239_1662+240i others(388): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
CCCCGAGT others(11): Show |
C | 2 | a0001c0001t0001g0238a0001c0001t0001g0246 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1662+243_1662+260d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
CCCCGAGT others(27): Show |
C | 1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1662+243_1662+276d others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288275
|
CCCCGAGT others(1864): Show |
C | 1 | a0011c0023t0001g0265 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1662+243_1663-121d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288275 | |||||
| chr1:1288276
|
CCCGAGTC others(159): Show |
C | 1 | a0014c0021t0008g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1662+240_1662+405d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288276 | ||||||
| chr1:1288276
|
CCCGAGTC others(1059): Show |
C | 1 | a0024c0033t0009g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1662+240_1663-929d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288276 | ||||||
| chr1:1288278
|
C | T | 7 | a0002c0003t0002g0061a0002c0003t0002g0101a0003c0004t0003g0004others(4): Show | 7 | HG01175.hp1 HG03209.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+241C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288278 | ||||||
| chr1:1288280
|
A | T | 133 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0237others(130): Show | 133 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1662+243A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288280 | ||||||
| chr1:1288284
|
T | C | 13 | a0001c0001t0001g0198a0001c0001t0002g0228a0001c0001t0002g0229others(10): Show | 13 | HG00597.hp2 HG01433.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662+247T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288284 | ||||||
| chr1:1288284
|
T | TGCTCCGT others(9): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+247_1662+248i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288284 | ||||||
| chr1:1288289
|
T | C | 21 | a0001c0001t0001g0243a0001c0001t0002g0233a0001c0012t0001g0127others(18): Show | 21 | HG01123.hp1 HG01169.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1662+252T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288289 | ||||||
| chr1:1288292
|
G | A | 1 | a0005c0011t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1662+255G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288292 | ||||||
| chr1:1288293
|
T | TCC | 6 | a0001c0001t0001g0237a0001c0001t0001g0250a0001c0020t0001g0263others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+258_1662+259d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288293 | |||||
| chr1:1288296
|
C | CCCGT | 8 | a0002c0002t0001g0029a0002c0002t0001g0094a0002c0003t0002g0064others(5): Show | 8 | HG00423.hp1 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1662+259_1662+260i others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288296 | ||||||
| chr1:1288296
|
C | CCCGTGTC others(55): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1662+259_1662+260i others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288296 | ||||||
| chr1:1288299
|
G | C | 12 | a0001c0001t0001g0207a0001c0009t0001g0218a0002c0002t0001g0029others(9): Show | 12 | HG00423.hp1 HG02300.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1662+262G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288299 | ||||||
| chr1:1288299
|
G | GTC | 89 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(86): Show | 89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1662+264_1662+265d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCCCTGC others(15): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1662+264_1662+265i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(69): Show |
1 | a0002c0002t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1662+265_1662+266i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(15): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1662+265_1662+266i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(13): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1662+265_1662+266i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(103): Show |
1 | a0003c0004t0003g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1662+265_1662+266i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(379): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1662+265_1662+266i others(388): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(103): Show |
2 | a0003c0004t0003g0145a0003c0004t0003g0152 | 2 | HG03490.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1662+265_1662+266i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
G | GTCTCTGC others(33): Show |
1 | a0002c0003t0004g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1662+265_1662+266i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288299
|
GTCTGCTC others(159): Show |
G | 1 | a0002c0003t0004g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1662+281_1662+446d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288299 | |||||
| chr1:1288300
|
T | TCC | 10 | a0001c0001t0001g0198a0001c0001t0002g0228a0001c0001t0002g0229others(7): Show | 10 | HG00597.hp2 HG01433.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662+264_1662+265i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288300 | |||||
| chr1:1288302
|
T | C | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0248others(5): Show | 8 | HG02132.hp1 HG03831.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+265T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288302 | ||||||
| chr1:1288302
|
TGCTCCGT others(9): Show |
T | 3 | a0005c0011t0001g0157a0008c0007t0004g0266a0008c0007t0004g0286 | 3 | HG02622.hp2 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1662+266_1662+281d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288302 | ||||||
| chr1:1288302
|
TGCTCCGT others(119): Show |
T | 1 | a0001c0001t0002g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1662+266_1662+391d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288302 | ||||||
| chr1:1288302
|
TGCTCCGT others(211): Show |
T | 1 | a0005c0011t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1662+266_1662+483d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288302 | ||||||
| chr1:1288305
|
T | C | 28 | a0001c0001t0001g0245a0001c0036t0006g0123a0002c0002t0001g0003others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1662+268T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288305 | ||||||
| chr1:1288308
|
G | A | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0248others(5): Show | 8 | HG02132.hp1 HG03831.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+271G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288308 | ||||||
| chr1:1288309
|
T | TCC | 16 | a0001c0001t0001g0244a0001c0001t0001g0245a0002c0002t0001g0008others(13): Show | 16 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1662+274_1662+275d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288309 | |||||
| chr1:1288309
|
T | TCCCCCGT others(93): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1662+275_1662+276i others(102): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288309 | |||||
| chr1:1288309
|
T | TTC | 8 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0248others(5): Show | 8 | HG02132.hp1 HG03831.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+272_1662+273i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288309 | ||||||
| chr1:1288312
|
C | T | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0248others(6): Show | 9 | HG02132.hp1 HG02300.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.1662+275C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288312 | ||||||
| chr1:1288314
|
T | A | 2 | a0003c0004t0003g0004a0003c0004t0003g0007 | 2 | NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1662+277T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288314 | ||||||
| chr1:1288316
|
TCC | T | 3 | a0001c0001t0001g0207a0001c0009t0001g0218a0016c0031t0001g0092 | 3 | HG02300.hp1 HG03579.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1662+281_1662+282d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288316 | |||||
| chr1:1288318
|
C | CCTGCTCC others(29): Show |
4 | a0001c0001t0001g0162a0001c0001t0002g0260a0001c0001t0005g0226others(1): Show | 4 | HG00735.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+303_1662+304i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288318 | |||||
| chr1:1288318
|
C | T | 101 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(98): Show | 101 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1662+281C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288318 | ||||||
| chr1:1288323
|
T | C | 17 | a0001c0036t0006g0123a0002c0002t0001g0084a0002c0003t0001g0063others(14): Show | 17 | HG00597.hp1 HG00642.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1662+286T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288323 | ||||||
| chr1:1288325
|
C | T | 1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+288C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288325 | ||||||
| chr1:1288326
|
G | A | 1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1662+289G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288326 | ||||||
| chr1:1288327
|
T | TCC | 6 | a0002c0002t0001g0003a0002c0002t0001g0055a0002c0003t0002g0015others(3): Show | 6 | HG00438.hp2 HG02293.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+292_1662+293d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288327 | |||||
| chr1:1288327
|
T | TCCCGTGT others(395): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1662+303_1662+304i others(404): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288327 | |||||
| chr1:1288330
|
C | T | 1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1662+293C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288330 | ||||||
| chr1:1288336
|
T | C | 10 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0009t0001g0218others(7): Show | 10 | HG00597.hp2 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662+299T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288336 | ||||||
| chr1:1288338
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1662+301T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288338 | ||||||
| chr1:1288341
|
C | CCCGTCCC others(237): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(246): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288341 | |||||
| chr1:1288341
|
C | CCCGTCCC others(83): Show |
1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288341 | |||||
| chr1:1288341
|
C | T | 108 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0198others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1662+304C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288341 | ||||||
| chr1:1288341
|
CCCGTCCC others(31): Show |
C | 1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1662+312_1662+349d others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288341 | |||||
| chr1:1288343
|
C | T | 1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1662+306C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288343 | ||||||
| chr1:1288344
|
G | A | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1662+307G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288344 | ||||||
| chr1:1288345
|
TCC | T | 49 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0245others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1662+312_1662+313d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288345 | |||||
| chr1:1288346
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1662+309C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288346 | ||||||
| chr1:1288347
|
C | CCCCGTGT others(31): Show |
4 | a0001c0001t0001g0162a0001c0001t0002g0260a0001c0001t0005g0226others(1): Show | 4 | HG00735.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+331_1662+332i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCCCGTGT others(333): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1662+331_1662+332i others(342): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCCCGTGT others(103): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1662+336_1662+337i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCCCGTGT others(599): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1662+336_1662+337i others(608): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCCCGTGT others(47): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1662+336_1662+337i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCC others(29): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCC others(29): Show |
1 | a0001c0012t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCC others(83): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(359): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(368): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(493): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(502): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(9): Show |
1 | a0001c0001t0001g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(49): Show |
4 | a0001c0001t0001g0252a0001c0018t0001g0251a0003c0004t0003g0171others(1): Show | 4 | HG02071.hp1 HG02165.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+311_1662+312i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(271): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(280): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(367): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(376): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(905): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(914): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(67): Show |
10 | a0001c0001t0002g0161a0001c0001t0002g0163a0001c0001t0002g0173others(7): Show | 10 | HG00280.hp1 HG00558.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662+311_1662+312i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(145): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(154): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(305): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(314): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(193): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(202): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(65): Show |
2 | a0002c0003t0004g0113a0002c0003t0004g0120 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1662+311_1662+312i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(83): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1662+311_1662+312i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288347
|
C | CCGTGTCT others(229): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1662+311_1662+312i others(238): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288347 | |||||
| chr1:1288350
|
C | T | 3 | a0002c0002t0001g0016a0002c0002t0001g0089a0005c0016t0001g0281 | 3 | HG01069.hp1 NA18969.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1662+313C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288350 | ||||||
| chr1:1288352
|
T | A | 14 | a0001c0001t0002g0169a0001c0001t0002g0228a0001c0001t0002g0229others(11): Show | 14 | HG00408.hp1 HG02132.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662+315T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288352 | ||||||
| chr1:1288355
|
C | CCCTGCTC others(9): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1662+318_1662+319i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288355 | ||||||
| chr1:1288355
|
C | CTCTGCTC others(9): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1662+321_1662+336d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288355 | |||||
| chr1:1288355
|
C | CTCTGCTC others(231): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1662+336_1662+337i others(240): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288355 | |||||
| chr1:1288356
|
T | C | 9 | a0001c0001t0001g0198a0001c0012t0001g0131a0002c0002t0001g0034others(6): Show | 9 | HG00597.hp1 HG00597.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1662+319T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288356 | ||||||
| chr1:1288356
|
T | TCTGCTCC others(777): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1662+336_1662+337i others(786): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288356 | |||||
| chr1:1288356
|
T | TCTGCTCC others(521): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1662+336_1662+337i others(530): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288356 | |||||
| chr1:1288356
|
TCTGCTCC others(11): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1662+391_1662+408d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288356 | |||||
| chr1:1288356
|
TCTGCTCC others(29): Show |
T | 6 | a0001c0001t0001g0178a0001c0001t0001g0196a0001c0001t0001g0200others(3): Show | 6 | HG01081.hp1 HG01169.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+373_1662+408d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288356 | |||||
| chr1:1288356
|
TCTGCTCC others(47): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1662+355_1662+408d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288356 | |||||
| chr1:1288361
|
T | C | 11 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0002g0236others(8): Show | 11 | HG02074.hp1 HG02135.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.1662+324T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288361 | ||||||
| chr1:1288361
|
T | TCCGTCCC others(11): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0217 | 3 | HG00741.hp1 HG01934.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1662+336_1662+337i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288361 | |||||
| chr1:1288361
|
T | TCCGTCCC others(121): Show |
1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1662+336_1662+337i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288361 | |||||
| chr1:1288361
|
T | TCCGTCCC others(103): Show |
2 | a0002c0003t0001g0026a0002c0003t0001g0069 | 2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1662+336_1662+337i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288361 | |||||
| chr1:1288364
|
G | A | 2 | a0008c0007t0004g0286a0008c0007t0004g0287 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1662+327G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288364 | ||||||
| chr1:1288365
|
T | TCC | 16 | a0001c0009t0001g0218a0002c0002t0001g0003a0002c0002t0001g0087others(13): Show | 16 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+330_1662+331d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288365 | |||||
| chr1:1288365
|
T | TCCCCCGT others(69): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1662+331_1662+332i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288365 | |||||
| chr1:1288365
|
T | TCCCGTGT others(13): Show |
5 | a0001c0001t0001g0001a0002c0003t0002g0012a0002c0003t0002g0099others(2): Show | 6 | HG01123.hp1 HG01256.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+336_1662+337i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288365 | |||||
| chr1:1288367
|
CCGTGTCC others(9): Show |
C | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1662+332_1662+347d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288367 | |||||
| chr1:1288368
|
C | T | 2 | a0008c0007t0004g0286a0008c0007t0004g0287 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1662+331C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288368 | ||||||
| chr1:1288369
|
G | C | 1 | a0001c0001t0001g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1662+332G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288369 | ||||||
| chr1:1288370
|
T | A | 2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1662+333T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288370 | ||||||
| chr1:1288370
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1662+333T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288370 | ||||||
| chr1:1288370
|
T | TGTCTCTG others(287): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1662+336_1662+337i others(296): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288370 | |||||
| chr1:1288372
|
TCC | T | 11 | a0001c0001t0002g0169a0001c0001t0002g0228a0001c0001t0002g0229others(8): Show | 11 | HG00408.hp1 HG01081.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+337_1662+338d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288372 | |||||
| chr1:1288373
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1662+336C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288373 | ||||||
| chr1:1288374
|
C | CCTGCTCC others(85): Show |
4 | a0002c0003t0002g0012a0002c0003t0002g0099a0004c0005t0002g0022others(1): Show | 4 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+349_1662+350i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288374 | |||||
| chr1:1288374
|
C | CCTGCTCC others(47): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+354_1662+355i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288374 | |||||
| chr1:1288374
|
C | CCTGCTCC others(141): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1662+354_1662+355i others(150): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288374 | |||||
| chr1:1288374
|
C | CCTGCTCC others(287): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1662+354_1662+355i others(296): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288374 | |||||
| chr1:1288374
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0165a0001c0001t0001g0167others(145): Show | 149 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1662+337C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288374 | ||||||
| chr1:1288379
|
T | C | 62 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0175others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1662+342T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288379 | ||||||
| chr1:1288382
|
G | A | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1662+345G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288382 | ||||||
| chr1:1288383
|
T | TCC | 14 | a0001c0001t0001g0245a0001c0001t0002g0225a0001c0012t0001g0131others(11): Show | 14 | HG00423.hp2 HG00597.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662+348_1662+349d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288383 | |||||
| chr1:1288383
|
T | TCCCCCGT others(184): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1662+349_1662+350i others(193): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288383 | |||||
| chr1:1288383
|
T | TCCCCCGT others(305): Show |
2 | a0002c0003t0002g0021a0002c0003t0002g0024 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1662+349_1662+350i others(314): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288383 | |||||
| chr1:1288383
|
T | TCCCGTGT others(309): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1662+354_1662+355i others(318): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288383 | |||||
| chr1:1288385
|
CCGTGTCC others(9): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1662+350_1662+365d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288385 | |||||
| chr1:1288385
|
CCGTGTCC others(439): Show |
C | 1 | a0002c0002t0001g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1662+350_1662+795d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288385 | |||||
| chr1:1288387
|
G | C | 1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+350G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288387 | ||||||
| chr1:1288388
|
T | A | 2 | a0001c0001t0002g0225a0004c0008t0001g0262 | 2 | HG01516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1662+351T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288388 | ||||||
| chr1:1288388
|
T | C | 1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+351T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288388 | ||||||
| chr1:1288390
|
TCC | T | 3 | a0004c0008t0001g0247a0006c0010t0007g0270a0006c0010t0007g0274 | 3 | HG00738.hp1 HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1662+355_1662+356d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288390 | |||||
| chr1:1288391
|
C | G | 1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+354C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288391 | ||||||
| chr1:1288392
|
C | CCTGCTCC others(47): Show |
1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1662+372_1662+373i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288392 | |||||
| chr1:1288392
|
C | T | 154 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0166others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1662+355C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288392 | ||||||
| chr1:1288392
|
CCTGCTCC others(423): Show |
C | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1662+373_1662+802d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288392 | |||||
| chr1:1288397
|
T | C | 35 | a0001c0001t0001g0168a0001c0001t0001g0242a0001c0012t0001g0130others(32): Show | 35 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1662+360T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288397 | ||||||
| chr1:1288397
|
T | TCCGTCCC others(49): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1662+367_1662+368i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288397 | |||||
| chr1:1288397
|
T | TCCGTCCC others(67): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1662+372_1662+373i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288397 | |||||
| chr1:1288397
|
T | TCCGTCCC others(67): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+372_1662+373i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288397 | |||||
| chr1:1288397
|
T | TCCGTCCC others(195): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1662+372_1662+373i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288397 | |||||
| chr1:1288401
|
T | TCC | 25 | a0001c0001t0001g0198a0001c0001t0001g0244a0001c0001t0002g0225others(22): Show | 25 | HG00099.hp2 HG01169.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1662+366_1662+367d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288401 | |||||
| chr1:1288401
|
T | TCCCCCGT others(253): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1662+367_1662+368i others(262): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288401 | |||||
| chr1:1288401
|
T | TCCCGTGT others(11): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+372_1662+373i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288401 | |||||
| chr1:1288401
|
TCCCGTGT others(49): Show |
T | 1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1662+373_1662+428d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288401 | |||||
| chr1:1288401
|
TCCCGTGT others(199): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1662+373_1662+578d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288401 | |||||
| chr1:1288401
|
TCCCGTGT others(219): Show |
T | 1 | a0004c0005t0010g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1662+373_1662+598d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288401 | |||||
| chr1:1288403
|
CCGTGTCC others(9): Show |
C | 2 | a0002c0002t0013g0075a0002c0003t0004g0117 | 2 | HG00423.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1662+368_1662+383d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288403 | |||||
| chr1:1288403
|
CCGTGTCC others(83): Show |
C | 1 | a0002c0002t0001g0065 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1662+368_1662+457d others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288403 | |||||
| chr1:1288403
|
CCGTGTCC others(235): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1662+368_1662+609d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288403 | |||||
| chr1:1288404
|
C | CGTGTCTC others(89): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+372_1662+373i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288404 | |||||
| chr1:1288406
|
T | A | 1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1662+369T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288406 | ||||||
| chr1:1288406
|
TGTCCCTG others(405): Show |
T | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1662+373_1662+784d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288406 | |||||
| chr1:1288408
|
TCC | T | 4 | a0003c0004t0003g0133a0003c0004t0003g0135a0003c0004t0003g0137others(1): Show | 4 | NA18964.hp2 NA18998.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+373_1662+374d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288408 | |||||
| chr1:1288409
|
C | CTCTGCCC others(29): Show |
1 | a0002c0002t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1662+372_1662+373i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288409 | ||||||
| chr1:1288410
|
C | CCTGCCCC others(334): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1662+377_1662+378i others(343): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288410 | |||||
| chr1:1288410
|
C | CCTGCTCC others(11): Show |
1 | a0001c0001t0001g0184 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1662+390_1662+391i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288410 | |||||
| chr1:1288410
|
C | CCTGCTCC others(67): Show |
3 | a0001c0001t0001g0252a0001c0001t0002g0163a0001c0018t0005g0224 | 3 | HG00558.hp1 NA18970.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1662+390_1662+391i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288410 | |||||
| chr1:1288410
|
C | CCTGCTCC others(29): Show |
2 | a0002c0003t0004g0113a0002c0003t0004g0120 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1662+390_1662+391i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288410 | |||||
| chr1:1288410
|
C | T | 162 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0167others(159): Show | 162 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1662+373C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288410 | ||||||
| chr1:1288412
|
T | C | 3 | a0003c0004t0003g0005a0003c0004t0003g0006a0003c0004t0003g0253 | 3 | HG01346.hp1 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1662+375T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288412 | ||||||
| chr1:1288415
|
T | C | 31 | a0001c0001t0001g0178a0001c0001t0001g0196a0001c0001t0001g0200others(28): Show | 31 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1662+378T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288415 | ||||||
| chr1:1288415
|
T | TCCGTCCC others(49): Show |
2 | a0001c0001t0001g0212a0001c0001t0001g0219 | 2 | HG00642.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1662+385_1662+386i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288415 | |||||
| chr1:1288415
|
T | TCCGTCCC others(345): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1662+385_1662+386i others(354): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288415 | |||||
| chr1:1288418
|
G | A | 4 | a0002c0003t0004g0118a0003c0004t0003g0005a0003c0004t0003g0006others(1): Show | 4 | HG01346.hp1 HG02970.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+381G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288418 | ||||||
| chr1:1288419
|
T | TCC | 40 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0177others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1662+384_1662+385d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(33): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1662+385_1662+386i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(339): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1662+385_1662+386i others(348): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(15): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1662+385_1662+386i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(55): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1662+385_1662+386i others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(51): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1662+385_1662+386i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(305): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1662+385_1662+386i others(314): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TCCCCCGT others(183): Show |
1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+385_1662+386i others(192): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288419 | |||||
| chr1:1288419
|
T | TTC | 4 | a0002c0003t0004g0118a0003c0004t0003g0005a0003c0004t0003g0006others(1): Show | 4 | HG01346.hp1 HG02970.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+382_1662+383i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288419 | ||||||
| chr1:1288421
|
CCGTGTCC others(9): Show |
C | 2 | a0001c0001t0001g0246a0004c0008t0001g0262 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1662+386_1662+401d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288421 | |||||
| chr1:1288422
|
C | T | 3 | a0003c0004t0003g0005a0003c0004t0003g0006a0003c0004t0003g0253 | 3 | HG01346.hp1 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1662+385C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288422 | ||||||
| chr1:1288423
|
G | C | 2 | a0001c0047t0001g0183a0002c0002t0001g0088 | 2 | HG00099.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1662+386G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288423 | ||||||
| chr1:1288424
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1662+387T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288424 | ||||||
| chr1:1288424
|
T | C | 2 | a0001c0047t0001g0183a0002c0002t0001g0088 | 2 | HG00099.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1662+387T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288424 | ||||||
| chr1:1288427
|
C | G | 2 | a0001c0047t0001g0183a0002c0002t0001g0088 | 2 | HG00099.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1662+390C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288427 | ||||||
| chr1:1288428
|
C | CCCGCTCC others(87): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+392_1662+393i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288428 | |||||
| chr1:1288428
|
C | T | 192 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(189): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1662+391C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288428 | ||||||
| chr1:1288433
|
T | C | 43 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0185others(40): Show | 43 | HG00280.hp1 HG00438.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1662+396T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288433 | ||||||
| chr1:1288437
|
T | TCC | 16 | a0001c0001t0001g0166a0001c0001t0001g0194a0001c0001t0001g0208others(13): Show | 16 | HG00280.hp2 HG00408.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+402_1662+403d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288437 | |||||
| chr1:1288439
|
CCGTGTCT others(29): Show |
C | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1662+404_1662+439d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288439 | |||||
| chr1:1288442
|
T | A | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1662+405T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288442 | ||||||
| chr1:1288442
|
T | TGTCTCTG others(31): Show |
1 | a0003c0004t0003g0145 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1662+413_1662+414i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288442 | |||||
| chr1:1288442
|
T | TGTCTCTG others(91): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+413_1662+414i others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288442 | |||||
| chr1:1288445
|
C | CTCTGCCC others(181): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+413_1662+414i others(190): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288445 | |||||
| chr1:1288445
|
C | G | 1 | a0014c0021t0008g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1662+408C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288445 | ||||||
| chr1:1288446
|
T | C | 13 | a0001c0001t0002g0254a0002c0002t0001g0034a0002c0002t0001g0049others(10): Show | 13 | HG01081.hp2 HG01928.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1662+409T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288446 | ||||||
| chr1:1288448
|
T | C | 2 | a0002c0003t0001g0060a0003c0004t0003g0139 | 2 | NA19072.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1662+411T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288448 | ||||||
| chr1:1288451
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0201a0001c0001t0001g0202others(39): Show | 43 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1662+414T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288451 | ||||||
| chr1:1288451
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288451 | |||||
| chr1:1288451
|
T | TCCGTCCC others(66): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(75): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288451 | |||||
| chr1:1288451
|
T | TCCGTCCC others(385): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(394): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288451 | |||||
| chr1:1288451
|
T | TCCGTCCC others(31): Show |
1 | a0003c0004t0003g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288451 | |||||
| chr1:1288451
|
T | TCCGTCCC others(67): Show |
2 | a0002c0003t0002g0021a0002c0003t0002g0024 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1662+421_1662+422i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288451 | |||||
| chr1:1288454
|
G | A | 4 | a0002c0002t0001g0035a0002c0002t0001g0037a0002c0003t0001g0060others(1): Show | 4 | NA18964.hp1 NA19004.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+417G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288454 | ||||||
| chr1:1288455
|
TCC | T | 62 | a0001c0001t0001g0167a0001c0001t0001g0177a0001c0001t0001g0198others(59): Show | 62 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1662+422_1662+423d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288455 | |||||
| chr1:1288456
|
C | A | 1 | a0002c0002t0001g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1662+419C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288456 | ||||||
| chr1:1288456
|
C | CCCGTGTC others(10): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288456 | |||||
| chr1:1288456
|
C | T | 4 | a0002c0002t0001g0035a0002c0002t0001g0037a0002c0003t0001g0060others(1): Show | 4 | NA18964.hp1 NA19004.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+419C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288456 | ||||||
| chr1:1288457
|
C | CCCCGAGT others(229): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1662+424_1662+425i others(238): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCCCGTGT others(11): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1662+452_1662+469d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCCCGTGT others(375): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1662+441_1662+442i others(384): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCCCGTGT others(419): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1662+469_1662+470i others(428): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCC others(27): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1662+421_1662+422i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCC others(161): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCC others(101): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0192a0001c0001t0001g0237a0002c0002t0001g0030 | 3 | HG01891.hp1 NA19080.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1662+421_1662+422i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(1015): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(1024): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(29): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(27): Show |
2 | a0001c0009t0001g0210a0001c0009t0001g0211 | 2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1662+421_1662+422i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(212): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(221): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(291): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(300): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(301): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(310): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(411): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(420): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(99): Show |
1 | a0002c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(108): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0165a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG00639.hp2 HG01070.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1662+421_1662+422i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(29): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(27): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(121): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(103): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(285): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(294): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(83): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1662+421_1662+422i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288457
|
C | CCGTGTCT others(259): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1662+421_1662+422i others(268): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288457 | |||||
| chr1:1288460
|
C | A | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662+423C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288460 | ||||||
| chr1:1288460
|
C | T | 4 | a0002c0003t0001g0060a0003c0004t0003g0139a0006c0010t0007g0270others(1): Show | 4 | HG00738.hp1 HG01496.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+423C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288460 | ||||||
| chr1:1288462
|
T | A | 12 | a0001c0001t0001g0184a0001c0001t0002g0228a0001c0001t0002g0248others(9): Show | 12 | HG00099.hp2 HG01346.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.1662+425T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288462 | ||||||
| chr1:1288466
|
T | C | 11 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0198others(8): Show | 11 | HG01255.hp2 HG01358.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+429T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288466 | ||||||
| chr1:1288466
|
T | TCTGCCCC others(107): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1662+433_1662+434i others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288466 | |||||
| chr1:1288471
|
T | C | 50 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0177others(47): Show | 50 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1662+434T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288471 | ||||||
| chr1:1288471
|
T | TCCGTCCC others(11): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+451_1662+452i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288471 | |||||
| chr1:1288475
|
T | TCC | 23 | a0001c0001t0001g0160a0001c0001t0001g0179a0001c0001t0001g0212others(20): Show | 23 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1662+440_1662+441d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288475 | |||||
| chr1:1288475
|
T | TCCCCCGA others(15): Show |
1 | a0003c0004t0003g0152 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1662+441_1662+442i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288475 | |||||
| chr1:1288475
|
T | TCCCCCGT others(33): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1662+441_1662+442i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288475 | |||||
| chr1:1288475
|
T | TCCCCCGT others(51): Show |
1 | a0002c0003t0004g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1662+441_1662+442i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288475 | |||||
| chr1:1288475
|
T | TCCCGTGT others(31): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1662+451_1662+452i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288475 | |||||
| chr1:1288477
|
CCGTGTCT others(9): Show |
C | 3 | a0003c0004t0003g0004a0003c0004t0003g0007a0009c0014t0001g0050 | 3 | HG03688.hp1 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1662+442_1662+457d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288477 | |||||
| chr1:1288480
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+443T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288480 | ||||||
| chr1:1288481
|
GTC | G | 4 | a0001c0001t0001g0184a0003c0004t0003g0005a0003c0004t0003g0006others(1): Show | 4 | HG01346.hp1 HG04199.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+448_1662+449d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288481 | |||||
| chr1:1288484
|
T | C | 10 | a0002c0002t0001g0041a0002c0002t0001g0055a0002c0002t0001g0109others(7): Show | 10 | HG02559.hp2 HG02809.hp2 HG03491.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662+447T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288484 | ||||||
| chr1:1288484
|
TCTGCTCC others(29): Show |
T | 2 | a0005c0011t0001g0156a0005c0011t0001g0157 | 2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1662+470_1662+505d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288484 | |||||
| chr1:1288489
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0185a0001c0001t0001g0189others(42): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1662+452T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288489 | ||||||
| chr1:1288489
|
T | TCCGTCCC others(123): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+464_1662+465i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288489 | |||||
| chr1:1288493
|
T | TCC | 27 | a0001c0001t0001g0179a0001c0001t0001g0193a0001c0001t0001g0198others(24): Show | 27 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.1662+458_1662+459d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288493
|
T | TCCCCCGT others(91): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1662+459_1662+460i others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288493
|
T | TCCCCCGT others(55): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1662+459_1662+460i others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288493
|
T | TCCCCCGT others(297): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1662+459_1662+460i others(306): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288493
|
T | TCCCGTGT others(87): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+477_1662+478i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288493
|
T | TCCCGTGT others(291): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+469_1662+470i others(300): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288493
|
TCCCGTGT others(69): Show |
T | 1 | a0001c0001t0001g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1662+470_1662+545d others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288493 | |||||
| chr1:1288494
|
CCCGTGTC others(10): Show |
C | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1662+460_1662+476d others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288494 | |||||
| chr1:1288494
|
CCCGTGTC others(144): Show |
C | 2 | a0006c0010t0007g0270a0006c0010t0007g0274 | 2 | HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1662+460_1662+610d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288494 | |||||
| chr1:1288495
|
CCGTGTCT others(9): Show |
C | 5 | a0001c0001t0001g0242a0002c0002t0001g0035a0002c0002t0001g0085others(2): Show | 5 | HG00423.hp2 HG02922.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+460_1662+475d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288495 | |||||
| chr1:1288496
|
C | T | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1662+459C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288496 | ||||||
| chr1:1288497
|
G | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1662+460G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288497 | ||||||
| chr1:1288498
|
T | A | 2 | a0003c0004t0003g0150a0006c0010t0007g0273 | 2 | HG00597.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1662+461T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288498 | ||||||
| chr1:1288498
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1662+461T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288498 | ||||||
| chr1:1288501
|
C | CCCTGCTC others(229): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1662+464_1662+465i others(238): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288501 | ||||||
| chr1:1288501
|
C | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1662+464C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288501 | ||||||
| chr1:1288502
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0208others(25): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1662+465T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288502 | ||||||
| chr1:1288507
|
C | CCCGTCCC others(305): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(314): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288507 | |||||
| chr1:1288507
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(140): Show | 144 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1662+470C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288507 | ||||||
| chr1:1288511
|
T | TCC | 39 | a0001c0001t0001g0208a0001c0001t0002g0225a0001c0001t0002g0233others(36): Show | 39 | HG00280.hp2 HG00621.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1662+476_1662+477d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288511 | |||||
| chr1:1288511
|
T | TCCCCCGT others(15): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1662+477_1662+478i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288511 | |||||
| chr1:1288511
|
T | TCCCGTGT others(13): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1662+476_1662+495d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288511 | |||||
| chr1:1288511
|
T | TCCCGTGT others(423): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1662+482_1662+483i others(432): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288511 | |||||
| chr1:1288511
|
T | TCCCGTGT others(195): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1662+482_1662+483i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288511 | |||||
| chr1:1288511
|
TCCCGTGT others(31): Show |
T | 3 | a0004c0008t0001g0239a0004c0008t0001g0240a0009c0013t0001g0078 | 3 | HG02258.hp1 HG02976.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1662+483_1662+520d others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288511 | |||||
| chr1:1288513
|
CCGTGTCC others(9): Show |
C | 1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+478_1662+493d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288513 | |||||
| chr1:1288516
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1662+479T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288516 | ||||||
| chr1:1288519
|
C | CTGCTCCG others(95): Show |
1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1662+482_1662+483i others(104): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288519 | ||||||
| chr1:1288520
|
C | CCTGCTCC others(193): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1662+505_1662+506i others(202): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288520 | |||||
| chr1:1288520
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0168others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1662+483C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288520 | ||||||
| chr1:1288525
|
T | C | 42 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0196others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1662+488T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288525 | ||||||
| chr1:1288525
|
T | TCCGTCCC others(85): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1662+495_1662+496i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288525 | |||||
| chr1:1288525
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1662+505_1662+506i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288525 | |||||
| chr1:1288529
|
T | TCC | 13 | a0001c0001t0001g0001a0001c0001t0001g0187a0001c0012t0001g0131others(10): Show | 14 | HG00099.hp2 HG01081.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662+494_1662+495d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288529 | |||||
| chr1:1288529
|
TCCCGTGT others(33): Show |
T | 1 | a0001c0001t0001g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1662+514_1662+553d others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288529 | |||||
| chr1:1288533
|
G | C | 2 | a0002c0002t0001g0102a0002c0003t0001g0044 | 2 | HG00544.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662+496G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288533 | ||||||
| chr1:1288534
|
T | C | 2 | a0002c0002t0001g0102a0002c0003t0001g0044 | 2 | HG00544.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662+497T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288534 | ||||||
| chr1:1288537
|
C | G | 2 | a0002c0002t0001g0102a0002c0003t0001g0044 | 2 | HG00544.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662+500C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288537 | ||||||
| chr1:1288538
|
T | C | 22 | a0001c0001t0001g0193a0001c0001t0001g0198a0001c0001t0001g0219others(19): Show | 22 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.1662+501T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288538 | ||||||
| chr1:1288538
|
TCTGCTCC others(1025): Show |
T | 1 | a0001c0020t0001g0176 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1662+514_1663-689d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288538 | |||||
| chr1:1288543
|
T | C | 50 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0196others(47): Show | 50 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1662+506T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288543 | ||||||
| chr1:1288544
|
C | T | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+507C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288544 | ||||||
| chr1:1288546
|
G | C | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+509G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288546 | ||||||
| chr1:1288547
|
T | G | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+510T>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288547 | ||||||
| chr1:1288547
|
TCC | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(81): Show | 85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1662+514_1662+515d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288547 | |||||
| chr1:1288547
|
TCCCCCGT others(15): Show |
T | 2 | a0002c0002t0001g0041a0003c0004t0003g0152 | 2 | NA18947.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1662+514_1662+535d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288547 | |||||
| chr1:1288547
|
TCCCCCGT others(147): Show |
T | 3 | a0003c0004t0003g0133a0003c0004t0003g0135a0003c0004t0003g0153 | 3 | NA18964.hp2 NA18998.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1662+514_1662+667d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288547 | |||||
| chr1:1288547
|
TCCCCCGT others(259): Show |
T | 1 | a0002c0002t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1662+514_1662+779d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288547 | |||||
| chr1:1288548
|
C | G | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+511C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288548 | ||||||
| chr1:1288549
|
C | CCCCGAGT others(47): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1662+516_1662+517i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCCCGTGT others(499): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1662+525_1662+526i others(508): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCCCGTGT others(49): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCCCGTGT others(575): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(584): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCCCGTGT others(325): Show |
1 | a0001c0001t0002g0230 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCCCGTGT others(399): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(408): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCC others(83): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCC others(45): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCC others(117): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(29): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(569): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(578): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(9): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(9): Show |
7 | a0001c0001t0002g0249a0001c0012t0001g0130a0002c0002t0001g0023others(4): Show | 7 | HG01175.hp1 HG02004.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+513_1662+514i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(29): Show |
2 | a0001c0036t0006g0123a0002c0003t0001g0018 | 2 | HG02738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1662+513_1662+514i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(85): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(283): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(292): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(63): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(159): Show |
2 | a0002c0003t0002g0099a0020c0030t0002g0103 | 2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1662+513_1662+514i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(155): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(101): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(158): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(167): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(27): Show |
1 | a0002c0002t0001g0030 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1662+513_1662+514i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(137): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CCGTGTCT others(99): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+513_1662+514i others(108): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288549 | |||||
| chr1:1288549
|
C | CGTGTCCC others(99): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1662+512_1662+513i others(108): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288549 | ||||||
| chr1:1288549
|
C | T | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+512C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288549 | ||||||
| chr1:1288554
|
T | A | 5 | a0001c0001t0001g0193a0001c0001t0001g0243a0005c0011t0001g0156others(2): Show | 5 | HG02451.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+517T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288554 | ||||||
| chr1:1288554
|
TGTCTCTG others(145): Show |
T | 1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1662+534_1662+685d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288554 | |||||
| chr1:1288555
|
GTC | G | 3 | a0001c0001t0001g0246a0004c0008t0001g0247a0009c0014t0001g0050 | 3 | HG02818.hp2 HG03139.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1662+522_1662+523d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288555 | |||||
| chr1:1288557
|
C | CTCTGCTC others(27): Show |
2 | a0002c0003t0002g0021a0002c0003t0002g0024 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1662+533_1662+534i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288557 | |||||
| chr1:1288557
|
C | CTCTGCTC others(29): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288557 | |||||
| chr1:1288557
|
C | G | 2 | a0004c0005t0006g0128a0004c0005t0010g0124 | 2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1662+520C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288557 | ||||||
| chr1:1288558
|
T | C | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0198others(12): Show | 15 | HG00597.hp2 HG01069.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1662+521T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288558 | ||||||
| chr1:1288558
|
TCTGCTCC others(987): Show |
T | 1 | a0001c0001t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1662+534_1663-707d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288558 | |||||
| chr1:1288563
|
T | C | 41 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0192others(38): Show | 41 | HG00423.hp1 HG00423.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1662+526T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288563 | ||||||
| chr1:1288563
|
T | TCCGTCCC others(11): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288563 | |||||
| chr1:1288563
|
T | TCCGTCCC others(435): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(444): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288563 | |||||
| chr1:1288563
|
T | TCCGTCCC others(215): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(224): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288563 | |||||
| chr1:1288565
|
C | T | 1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1662+528C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288565 | ||||||
| chr1:1288567
|
TCC | T | 92 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0177others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1662+534_1662+535d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288567 | |||||
| chr1:1288567
|
TCCCCCGT others(33): Show |
T | 3 | a0002c0002t0001g0057a0002c0002t0001g0062a0002c0002t0001g0076 | 3 | HG00673.hp1 HG02074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1662+534_1662+573d others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288567 | |||||
| chr1:1288567
|
TCCCCCGT others(127): Show |
T | 1 | a0002c0002t0001g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1662+534_1662+667d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288567 | |||||
| chr1:1288569
|
C | CCCCGAGT others(325): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1662+536_1662+537i others(334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCCCGTGT others(107): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1662+540_1662+541i others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCCCGTGT others(29): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+563_1662+564i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCCCGTGT others(103): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1662+541_1662+542i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCC others(117): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCC others(117): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0001a0002c0003t0004g0119a0004c0008t0001g0241 | 4 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+533_1662+534i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(65): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(831): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(840): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(43): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(52): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(9): Show |
1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(299): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(308): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(521): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(530): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(27): Show |
4 | a0001c0001t0001g0165a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG00639.hp2 HG01070.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+533_1662+534i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(251): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(260): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(27): Show |
2 | a0001c0012t0001g0131a0002c0003t0002g0064 | 2 | HG01517.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1662+533_1662+534i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(63): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(63): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(189): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(198): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(81): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1662+533_1662+534i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288569
|
C | CCGTGTCT others(7): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1662+533_1662+534i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288569 | |||||
| chr1:1288574
|
T | A | 6 | a0003c0004t0003g0146a0003c0004t0003g0149a0003c0004t0003g0154others(3): Show | 6 | HG02074.hp1 HG02559.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+537T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288574 | ||||||
| chr1:1288575
|
GTC | G | 4 | a0002c0002t0001g0109a0004c0008t0001g0239a0004c0008t0001g0240others(1): Show | 4 | HG02258.hp1 HG02976.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+542_1662+543d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288575 | |||||
| chr1:1288577
|
C | G | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1662+540C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288577 | ||||||
| chr1:1288578
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0165a0001c0001t0001g0180others(21): Show | 25 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.1662+541T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288578 | ||||||
| chr1:1288578
|
T | TGCTCCGT others(472): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1662+541_1662+542i others(481): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288578 | ||||||
| chr1:1288583
|
T | C | 39 | a0001c0001t0001g0179a0001c0001t0001g0200a0001c0001t0001g0201others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1662+546T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288583 | ||||||
| chr1:1288583
|
T | TCCGTCCC others(89): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1662+553_1662+554i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288583 | |||||
| chr1:1288587
|
T | TCC | 19 | a0001c0001t0001g0177a0001c0009t0001g0205a0001c0009t0001g0218others(16): Show | 19 | HG01123.hp2 HG01257.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.1662+552_1662+553d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288587 | |||||
| chr1:1288587
|
T | TCCCGTGT others(129): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1662+563_1662+564i others(138): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288587 | |||||
| chr1:1288589
|
CCGTGTCT others(49): Show |
C | 1 | a0002c0002t0001g0037 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1662+554_1662+609d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288589 | |||||
| chr1:1288589
|
CCGTGTCT others(159): Show |
C | 1 | a0002c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1662+554_1662+719d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288589 | |||||
| chr1:1288592
|
TGTCTCTG others(107): Show |
T | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1662+572_1662+685d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288592 | |||||
| chr1:1288596
|
T | C | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0011g0268others(12): Show | 15 | HG00558.hp2 HG00597.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1662+559T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288596 | ||||||
| chr1:1288596
|
T | TCTGCTCC others(197): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(206): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288596 | |||||
| chr1:1288598
|
T | C | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1662+561T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288598 | ||||||
| chr1:1288600
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+563C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288600 | ||||||
| chr1:1288601
|
T | C | 64 | a0001c0001t0001g0177a0001c0001t0001g0184a0001c0001t0001g0193others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1662+564T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288601 | ||||||
| chr1:1288601
|
T | TCCGTCCC others(103): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288601 | |||||
| chr1:1288601
|
T | TCCGTCCC others(375): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(384): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288601 | |||||
| chr1:1288604
|
G | A | 4 | a0001c0001t0011g0268a0002c0003t0004g0111a0002c0003t0004g0117others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+567G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288604 | ||||||
| chr1:1288605
|
TCC | T | 78 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0001g0178others(75): Show | 78 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1662+572_1662+573d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288605 | |||||
| chr1:1288605
|
TCCCCCGT others(15): Show |
T | 4 | a0002c0002t0001g0079a0002c0003t0001g0091a0003c0004t0003g0137others(1): Show | 4 | HG02155.hp2 NA19005.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+572_1662+593d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288605 | |||||
| chr1:1288605
|
TCCCCCGT others(89): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1662+572_1662+667d others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288605 | |||||
| chr1:1288606
|
C | G | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+569C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288606 | ||||||
| chr1:1288606
|
C | T | 4 | a0001c0001t0011g0268a0002c0003t0004g0111a0002c0003t0004g0117others(1): Show | 4 | HG01884.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+569C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288606 | ||||||
| chr1:1288607
|
C | CCCCGAGT others(29): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1662+574_1662+575i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCCCGTGT others(11): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+583_1662+584i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCCCGTGT others(29): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCCCGTGT others(29): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCC others(9): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCC others(197): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(206): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCC others(45): Show |
1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(49): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(27): Show |
2 | a0001c0001t0001g0193a0003c0004t0003g0150 | 2 | HG02071.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1662+571_1662+572i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(441): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(450): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(27): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(9): Show |
1 | a0001c0012t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(125): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(29): Show |
2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1662+571_1662+572i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(195): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(27): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(251): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(260): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(85): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1662+571_1662+572i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | CCGTGTCT others(45): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1662+571_1662+572i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288607 | |||||
| chr1:1288607
|
C | T | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+570C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288607 | ||||||
| chr1:1288610
|
C | T | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1662+573C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288610 | ||||||
| chr1:1288612
|
T | A | 2 | a0003c0004t0003g0144a0003c0004t0003g0148 | 2 | HG02896.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1662+575T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288612 | ||||||
| chr1:1288616
|
T | C | 11 | a0001c0001t0001g0208a0001c0047t0001g0183a0002c0002t0001g0019others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+579T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288616 | ||||||
| chr1:1288620
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1662+583C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288620 | ||||||
| chr1:1288621
|
T | C | 70 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0185others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1662+584T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288621 | ||||||
| chr1:1288621
|
T | TCCGGTCC others(128): Show |
1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1662+587_1662+588i others(137): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288621 | |||||
| chr1:1288621
|
T | TCCGTCCC others(13): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1662+592_1662+611d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288621 | |||||
| chr1:1288621
|
T | TCCGTCCC others(11): Show |
2 | a0001c0001t0002g0163a0002c0002t0001g0068 | 2 | HG00558.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1662+591_1662+592i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288621 | |||||
| chr1:1288621
|
T | TCCGTCCC others(31): Show |
2 | a0002c0002t0001g0055a0008c0007t0004g0285 | 2 | HG02970.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1662+591_1662+592i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288621 | |||||
| chr1:1288625
|
TCC | T | 98 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0177others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1662+592_1662+593d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288625 | |||||
| chr1:1288625
|
TCCCCCGT others(311): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1662+592_1662+909d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288625 | |||||
| chr1:1288627
|
C | CCCCGTGT others(271): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1662+652_1662+653i others(280): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+603_1662+604i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCCCGTGT others(29): Show |
1 | a0003c0004t0003g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1662+603_1662+604i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCC others(9): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCC others(45): Show |
1 | a0002c0002t0001g0042 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1662+591_1662+592i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCC others(9): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1662+591_1662+592i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(9): Show |
1 | a0002c0002t0001g0030 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1662+591_1662+592i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1662+591_1662+592i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(83): Show |
1 | a0002c0003t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(101): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(9): Show |
2 | a0001c0001t0001g0204a0001c0001t0005g0226 | 2 | HG01975.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1662+591_1662+592i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(515): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(524): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(161): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1662+591_1662+592i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288627
|
C | CCGTGTCT others(431): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1662+591_1662+592i others(440): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288627 | |||||
| chr1:1288630
|
C | T | 1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+593C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288630 | ||||||
| chr1:1288632
|
T | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0192a0001c0001t0001g0208 | 3 | HG00280.hp2 HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1662+595T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288632 | ||||||
| chr1:1288635
|
C | G | 1 | a0009c0013t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1662+598C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288635 | ||||||
| chr1:1288636
|
T | C | 19 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0250others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1662+599T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288636 | ||||||
| chr1:1288636
|
T | TCTGCCCC others(11): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1662+616_1662+617i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288636 | |||||
| chr1:1288636
|
T | TGCTCCGT others(235): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1662+599_1662+600i others(244): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288636 | ||||||
| chr1:1288641
|
C | CCCGTCCC others(315): Show |
2 | a0002c0003t0002g0012a0020c0030t0002g0103 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1662+611_1662+612i others(324): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288641 | |||||
| chr1:1288641
|
C | CCCGTCCC others(121): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1662+726_1662+727i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288641 | |||||
| chr1:1288641
|
C | T | 110 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0175others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1662+604C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288641 | ||||||
| chr1:1288641
|
CCCGTCCC others(11): Show |
C | 1 | a0003c0004t0003g0006 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1662+635_1662+652d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288641 | |||||
| chr1:1288641
|
CCCGTCCC others(103): Show |
C | 2 | a0002c0002t0001g0059a0009c0013t0001g0078 | 2 | NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1662+617_1662+726d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288641 | |||||
| chr1:1288643
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+606C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288643 | ||||||
| chr1:1288644
|
G | A | 2 | a0002c0002t0001g0019a0002c0003t0004g0115 | 2 | HG01358.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1662+607G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288644 | ||||||
| chr1:1288645
|
T | TCC | 20 | a0001c0001t0001g0178a0001c0001t0001g0244a0001c0001t0002g0163others(17): Show | 20 | HG00438.hp1 HG00558.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1662+610_1662+611d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288645 | |||||
| chr1:1288645
|
T | TCCCCCGT others(111): Show |
1 | a0002c0002t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1662+611_1662+612i others(120): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288645 | |||||
| chr1:1288645
|
T | TCCCGTGT others(13): Show |
1 | a0002c0003t0002g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1662+621_1662+622i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288645 | |||||
| chr1:1288647
|
CCGTGTCT others(9): Show |
C | 1 | a0001c0001t0002g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1662+612_1662+627d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288647 | |||||
| chr1:1288647
|
CCGTGTCT others(119): Show |
C | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1662+612_1662+737d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288647 | |||||
| chr1:1288648
|
C | T | 2 | a0006c0010t0007g0270a0006c0010t0007g0274 | 2 | HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1662+611C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288648 | ||||||
| chr1:1288649
|
G | C | 1 | a0004c0008t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1662+612G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288649 | ||||||
| chr1:1288650
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1662+613T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288650 | ||||||
| chr1:1288650
|
T | C | 1 | a0004c0008t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1662+613T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288650 | ||||||
| chr1:1288650
|
TGTCTCTG others(291): Show |
T | 1 | a0005c0011t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1662+653_1662+950d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288650 | |||||
| chr1:1288653
|
C | CTCTGCCC others(29): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1662+621_1662+622i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288653 | |||||
| chr1:1288653
|
C | G | 1 | a0004c0008t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1662+616C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288653 | ||||||
| chr1:1288654
|
T | C | 19 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0001g0203others(16): Show | 19 | HG00099.hp2 HG00735.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1662+617T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288654 | ||||||
| chr1:1288654
|
T | TCTGCTCC others(125): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1662+624_1662+625i others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288654 | |||||
| chr1:1288654
|
TCTGCTCC others(891): Show |
T | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1662+635_1663-702d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288654 | |||||
| chr1:1288659
|
T | C | 61 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0198others(58): Show | 61 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+622T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288659 | ||||||
| chr1:1288661
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1662+624C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288661 | ||||||
| chr1:1288663
|
T | TCC | 36 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0002g0173others(33): Show | 36 | HG00558.hp2 HG01109.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.1662+628_1662+629d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288663 | |||||
| chr1:1288663
|
T | TCCCCCGT others(15): Show |
1 | a0001c0001t0001g0202 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1662+629_1662+630i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288663 | |||||
| chr1:1288663
|
T | TCCCGTGT others(51): Show |
1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1662+639_1662+640i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288663 | |||||
| chr1:1288663
|
T | TCCCGTGT others(33): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1662+647_1662+648i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288663 | |||||
| chr1:1288663
|
TCCCGTGT others(667): Show |
T | 2 | a0002c0002t0001g0057a0002c0002t0001g0062 | 2 | HG00673.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1662+648_1663-913d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288663 | |||||
| chr1:1288664
|
CCCGTGTC others(48): Show |
C | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+630_1662+684d others(57): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288664 | |||||
| chr1:1288665
|
CCGTGTCT others(9): Show |
C | 2 | a0002c0003t0001g0060a0003c0004t0003g0141 | 2 | HG03540.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1662+630_1662+645d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288665 | |||||
| chr1:1288665
|
CCGTGTCT others(47): Show |
C | 1 | a0002c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1662+630_1662+683d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288665 | |||||
| chr1:1288665
|
CCGTGTCT others(101): Show |
C | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1662+630_1662+737d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288665 | |||||
| chr1:1288666
|
C | CGTGTCTG others(11): Show |
1 | a0003c0004t0003g0171 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1662+635_1662+636i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288666 | |||||
| chr1:1288667
|
G | A | 1 | a0003c0004t0003g0145 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1662+630G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288667 | ||||||
| chr1:1288667
|
G | C | 1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+630G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288667 | ||||||
| chr1:1288668
|
T | A | 1 | a0003c0004t0003g0151 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1662+631T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288668 | ||||||
| chr1:1288668
|
T | C | 1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+631T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288668 | ||||||
| chr1:1288668
|
TGTCTCTG others(143): Show |
T | 1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1662+653_1662+802d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288668 | |||||
| chr1:1288668
|
TGTCTCTG others(403): Show |
T | 1 | a0002c0002t0001g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1662+648_1662+1057 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288668 | |||||
| chr1:1288671
|
C | CTCTGCTC others(11): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+647_1662+648i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288671 | |||||
| chr1:1288671
|
C | G | 1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+634C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288671 | ||||||
| chr1:1288672
|
T | C | 29 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0197others(26): Show | 29 | HG00438.hp1 HG00597.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1662+635T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288672 | ||||||
| chr1:1288672
|
T | TCTGCCCC others(105): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1662+639_1662+640i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288672 | |||||
| chr1:1288672
|
T | TCTGCTCC others(221): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+652_1662+653i others(230): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288672 | |||||
| chr1:1288676
|
CTCCGTCC others(123): Show |
C | 1 | a0002c0002t0001g0076 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1662+648_1662+777d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288676 | |||||
| chr1:1288677
|
T | C | 39 | a0001c0001t0001g0177a0001c0001t0001g0184a0001c0001t0001g0185others(36): Show | 39 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1662+640T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288677 | ||||||
| chr1:1288680
|
G | A | 3 | a0002c0003t0004g0113a0002c0003t0004g0116a0007c0006t0001g0070 | 3 | HG01243.hp1 HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1662+643G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288680 | ||||||
| chr1:1288681
|
T | TCC | 29 | a0001c0001t0001g0175a0001c0001t0001g0195a0001c0001t0001g0202others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1662+646_1662+647d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288681 | |||||
| chr1:1288681
|
T | TCCCCCGT others(15): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1662+647_1662+648i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288681 | |||||
| chr1:1288681
|
T | TCCCCCGT others(33): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1662+647_1662+648i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288681 | |||||
| chr1:1288681
|
T | TCCCGTGT others(143): Show |
1 | a0002c0003t0002g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1662+652_1662+653i others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288681 | |||||
| chr1:1288681
|
T | TTC | 3 | a0002c0003t0004g0113a0002c0003t0004g0116a0007c0006t0001g0070 | 3 | HG01243.hp1 HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1662+644_1662+645i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288681 | ||||||
| chr1:1288683
|
CCGTGTCC others(141): Show |
C | 1 | a0002c0002t0001g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1662+648_1662+795d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288683 | |||||
| chr1:1288683
|
CCGTGTCC others(439): Show |
C | 1 | a0002c0002t0001g0079 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1662+648_1662+1093 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288683 | |||||
| chr1:1288685
|
G | C | 4 | a0001c0001t0001g0243a0001c0047t0001g0183a0002c0002t0001g0080others(1): Show | 4 | HG00099.hp2 HG02451.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+648G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288685 | ||||||
| chr1:1288686
|
T | A | 4 | a0001c0001t0001g0213a0003c0004t0003g0138a0003c0004t0003g0142others(1): Show | 4 | HG00558.hp2 HG03927.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+649T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288686 | ||||||
| chr1:1288686
|
T | C | 4 | a0001c0001t0001g0243a0001c0047t0001g0183a0002c0002t0001g0080others(1): Show | 4 | HG00099.hp2 HG02451.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+649T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288686 | ||||||
| chr1:1288686
|
TGTCCCTG others(13): Show |
T | 3 | a0001c0001t0001g0196a0001c0001t0011g0268a0010c0019t0003g0098 | 3 | HG02015.hp2 HG03225.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1662+653_1662+672d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288686 | |||||
| chr1:1288686
|
TGTCCCTG others(125): Show |
T | 2 | a0002c0002t0001g0096a0018c0027t0001g0020 | 2 | NA18980.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1662+653_1662+784d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288686 | |||||
| chr1:1288686
|
TGTCCCTG others(255): Show |
T | 1 | a0004c0005t0006g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1662+653_1662+914d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288686 | |||||
| chr1:1288687
|
GTCCCTGC others(387): Show |
G | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1662+653_1662+1046 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288687 | |||||
| chr1:1288689
|
C | G | 4 | a0001c0001t0001g0243a0001c0047t0001g0183a0002c0002t0001g0080others(1): Show | 4 | HG00099.hp2 HG02451.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+652C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288689 | ||||||
| chr1:1288690
|
C | CCTGCTCC others(47): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288690 | |||||
| chr1:1288690
|
C | T | 184 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0177others(181): Show | 184 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1662+653C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288690 | ||||||
| chr1:1288690
|
CCTGCTCC others(13): Show |
C | 2 | a0003c0004t0003g0143a0005c0016t0001g0281 | 2 | HG01069.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1662+666_1662+685d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288690 | |||||
| chr1:1288692
|
T | C | 1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1662+655T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288692 | ||||||
| chr1:1288695
|
T | C | 50 | a0001c0001t0001g0162a0001c0001t0002g0140a0001c0001t0002g0225others(47): Show | 50 | HG00621.hp1 HG00735.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.1662+658T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288695 | ||||||
| chr1:1288695
|
T | TCCGTCCC others(411): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(420): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288695 | |||||
| chr1:1288695
|
T | TCCGTCCC others(65): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288695 | |||||
| chr1:1288698
|
G | A | 2 | a0002c0003t0004g0118a0021c0032t0002g0039 | 2 | HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1662+661G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288698 | ||||||
| chr1:1288699
|
TCC | T | 89 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0184others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1662+666_1662+667d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288699 | |||||
| chr1:1288699
|
TCCCCCGA others(14): Show |
T | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1662+665_1662+685d others(23): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288699 | |||||
| chr1:1288700
|
C | CCCGTGTC others(103): Show |
1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288700 | |||||
| chr1:1288700
|
C | T | 2 | a0002c0003t0004g0118a0021c0032t0002g0039 | 2 | HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1662+663C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288700 | ||||||
| chr1:1288701
|
C | CCATGTCT others(47): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCCCGTGT others(261): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1662+668_1662+669i others(270): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCCCGTGT others(29): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1662+668_1662+669i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCC others(9): Show |
2 | a0001c0018t0001g0251a0023c0045t0001g0164 | 2 | HG02071.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1662+665_1662+666i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCC others(117): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCC others(65): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCC others(65): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCC others(283): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(292): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCC others(45): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(9): Show |
2 | a0002c0003t0004g0111a0002c0003t0004g0119 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1662+665_1662+666i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(137): Show |
1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(195): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(47): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(287): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1662+665_1662+666i others(296): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
C | CCGTGTCT others(7): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1662+665_1662+666i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288701
|
CCCCGAGT others(47): Show |
C | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1662+669_1662+722d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288701 | |||||
| chr1:1288704
|
C | T | 2 | a0008c0007t0004g0286a0021c0032t0002g0039 | 2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1662+667C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288704 | ||||||
| chr1:1288704
|
CGAGTCTC others(125): Show |
C | 1 | a0005c0011t0001g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1662+669_1662+800d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288704 | |||||
| chr1:1288706
|
A | T | 211 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(208): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1662+669A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288706 | ||||||
| chr1:1288706
|
AGTCTCTG others(11): Show |
A | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+709_1662+726d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288706 | |||||
| chr1:1288709
|
C | CTCTGCTC others(9): Show |
1 | a0001c0001t0005g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1662+676_1662+691d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288709 | |||||
| chr1:1288709
|
C | G | 2 | a0006c0010t0007g0270a0006c0010t0007g0274 | 2 | HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1662+672C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288709 | ||||||
| chr1:1288710
|
T | C | 18 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0001g0202others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.1662+673T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288710 | ||||||
| chr1:1288710
|
T | TCTGCCCC others(85): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1662+677_1662+678i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288710 | |||||
| chr1:1288710
|
T | TCTGCCCC others(105): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1662+677_1662+678i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288710 | |||||
| chr1:1288715
|
T | C | 35 | a0001c0001t0001g0187a0001c0001t0001g0200a0001c0001t0001g0202others(32): Show | 35 | HG00558.hp1 HG01070.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1662+678T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288715 | ||||||
| chr1:1288719
|
T | TCC | 39 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0001g0197others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.1662+684_1662+685d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288719 | |||||
| chr1:1288719
|
T | TCCCATGT others(13): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1662+685_1662+686i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288719 | |||||
| chr1:1288719
|
T | TCCCCCGT others(93): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1662+685_1662+686i others(102): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288719 | |||||
| chr1:1288719
|
T | TCCCGTGT others(13): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+695_1662+696i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288719 | |||||
| chr1:1288719
|
T | TCCCGTGT others(89): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1662+695_1662+696i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288719 | |||||
| chr1:1288721
|
CCGTGTCT others(9): Show |
C | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1662+686_1662+701d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288721 | |||||
| chr1:1288723
|
G | A | 2 | a0001c0001t0001g0202a0002c0002t0001g0084 | 2 | HG01070.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1662+686G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288723 | ||||||
| chr1:1288723
|
G | C | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+686G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288723 | ||||||
| chr1:1288724
|
T | A | 1 | a0013c0042t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1662+687T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288724 | ||||||
| chr1:1288724
|
T | C | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+687T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288724 | ||||||
| chr1:1288724
|
T | TGTCTCTG others(49): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+708_1662+709i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288724 | |||||
| chr1:1288724
|
TGTCTCTG others(87): Show |
T | 2 | a0001c0001t0011g0268a0003c0004t0003g0006 | 2 | HG01346.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1662+727_1662+820d others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288724 | |||||
| chr1:1288724
|
TGTCTCTG others(217): Show |
T | 1 | a0002c0002t0001g0067 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1662+727_1662+950d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288724 | |||||
| chr1:1288727
|
C | G | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+690C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288727 | ||||||
| chr1:1288728
|
T | C | 24 | a0001c0001t0001g0188a0001c0001t0001g0196a0001c0001t0001g0245others(21): Show | 24 | HG00738.hp1 HG01081.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1662+691T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288728 | ||||||
| chr1:1288728
|
T | TCTGCTCC others(121): Show |
1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+726_1662+727i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288728 | |||||
| chr1:1288732
|
CTCCGTCC others(67): Show |
C | 1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+704_1662+777d others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288732 | |||||
| chr1:1288733
|
T | C | 52 | a0001c0001t0001g0203a0001c0001t0001g0222a0001c0001t0001g0223others(49): Show | 52 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1662+696T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288733 | ||||||
| chr1:1288733
|
T | TCCGTCCC others(107): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1662+703_1662+704i others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288733 | |||||
| chr1:1288733
|
T | TCCGTCCC others(49): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+703_1662+704i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288733 | |||||
| chr1:1288737
|
T | TCC | 40 | a0001c0001t0001g0195a0001c0001t0001g0202a0001c0001t0001g0203others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1662+702_1662+703d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288737
|
T | TCCCCCGT others(15): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+703_1662+704i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288737
|
T | TCCCCCGT others(69): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+703_1662+704i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288737
|
T | TCCCCCGT others(15): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1662+703_1662+704i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288737
|
T | TCCCCCGT others(221): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1662+703_1662+704i others(230): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288737
|
T | TCCCGTGT others(31): Show |
1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1662+708_1662+709i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288737
|
T | TCCCGTGT others(147): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1662+713_1662+714i others(156): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288737 | |||||
| chr1:1288740
|
C | CCCGTGTC others(69): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1662+703_1662+704i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288740 | ||||||
| chr1:1288741
|
G | C | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662+704G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288741 | ||||||
| chr1:1288742
|
T | A | 2 | a0002c0002t0001g0008a0013c0042t0001g0129 | 2 | NA18951.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1662+705T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288742 | ||||||
| chr1:1288742
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662+705T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288742 | ||||||
| chr1:1288742
|
T | TGTCTCTG others(161): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+721_1662+722i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288742 | |||||
| chr1:1288742
|
TGTCTCTG others(69): Show |
T | 1 | a0002c0002t0001g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1662+727_1662+802d others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288742 | |||||
| chr1:1288742
|
TGTCTCTG others(199): Show |
T | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1662+727_1662+932d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288742 | |||||
| chr1:1288745
|
C | G | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662+708C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288745 | ||||||
| chr1:1288746
|
T | C | 20 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0193others(17): Show | 20 | HG00280.hp2 HG00621.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1662+709T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288746 | ||||||
| chr1:1288750
|
CTCCGTCC others(49): Show |
C | 1 | a0004c0005t0010g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1662+722_1662+777d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288750 | |||||
| chr1:1288751
|
T | C | 54 | a0001c0001t0001g0162a0001c0001t0001g0192a0001c0001t0001g0198others(51): Show | 54 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1662+714T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288751 | ||||||
| chr1:1288754
|
G | A | 1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1662+717G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288754 | ||||||
| chr1:1288755
|
T | TCC | 37 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0001g0202others(34): Show | 37 | HG00280.hp2 HG00597.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1662+720_1662+721d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288755 | |||||
| chr1:1288755
|
T | TCCCCCGT others(55): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1662+721_1662+722i others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288755 | |||||
| chr1:1288755
|
T | TCCCCCGT others(293): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1662+721_1662+722i others(302): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288755 | |||||
| chr1:1288755
|
T | TCCCGTGT others(33): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1662+726_1662+727i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288755 | |||||
| chr1:1288755
|
T | TCCCGTGT others(13): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1662+726_1662+727i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288755 | |||||
| chr1:1288755
|
T | TCCCGTGT others(141): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1662+726_1662+727i others(150): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288755 | |||||
| chr1:1288755
|
T | TTCCCCGT others(15): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1662+718_1662+719i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288755 | ||||||
| chr1:1288757
|
CCGTGTCC others(9): Show |
C | 3 | a0002c0002t0001g0042a0003c0004t0003g0148a0003c0004t0003g0152 | 3 | HG02896.hp2 NA18967.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1662+722_1662+737d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288757 | |||||
| chr1:1288757
|
CCGTGTCC others(85): Show |
C | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1662+722_1662+813d others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288757 | |||||
| chr1:1288757
|
CCGTGTCC others(103): Show |
C | 2 | a0003c0004t0003g0005a0014c0021t0008g0271 | 2 | NA19007.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1662+722_1662+831d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288757 | |||||
| chr1:1288757
|
CCGTGTCC others(1382): Show |
C | 1 | a0003c0034t0009g0279 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1662+722_1663-124d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288757 | |||||
| chr1:1288758
|
C | CGTGTCTC others(13): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1662+726_1662+727i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288758 | |||||
| chr1:1288759
|
G | C | 2 | a0004c0008t0001g0239a0004c0008t0001g0240 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1662+722G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288759 | ||||||
| chr1:1288760
|
T | A | 3 | a0001c0001t0001g0208a0001c0001t0002g0254a0023c0045t0001g0164 | 3 | HG00280.hp2 HG03195.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1662+723T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288760 | ||||||
| chr1:1288760
|
T | C | 2 | a0004c0008t0001g0239a0004c0008t0001g0240 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1662+723T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288760 | ||||||
| chr1:1288760
|
TGTCCCTG others(51): Show |
T | 4 | a0001c0001t0001g0223a0001c0012t0001g0130a0003c0004t0003g0141others(1): Show | 4 | HG01261.hp1 HG03540.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+727_1662+784d others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288760 | |||||
| chr1:1288760
|
TGTCCCTG others(181): Show |
T | 1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1662+727_1662+914d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288760 | |||||
| chr1:1288763
|
C | CTCTGCTC others(67): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1662+726_1662+727i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288763 | ||||||
| chr1:1288763
|
C | G | 2 | a0004c0008t0001g0239a0004c0008t0001g0240 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1662+726C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288763 | ||||||
| chr1:1288764
|
C | CCTGCTCC others(125): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1662+739_1662+740i others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288764 | |||||
| chr1:1288764
|
C | CCTGCTCC others(49): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1662+739_1662+740i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288764 | |||||
| chr1:1288764
|
C | CCTGCTCC others(10): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1662+738_1662+739i others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288764 | |||||
| chr1:1288764
|
C | T | 157 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(154): Show | 157 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1662+727C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288764 | ||||||
| chr1:1288764
|
CCTGCTCC others(181): Show |
C | 1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1662+758_1662+945d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288764 | |||||
| chr1:1288769
|
T | C | 39 | a0001c0001t0001g0162a0001c0001t0001g0185a0001c0001t0001g0196others(36): Show | 39 | HG00423.hp2 HG00438.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1662+732T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288769 | ||||||
| chr1:1288769
|
T | TCCGTCCC others(49): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1662+744_1662+745i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288769 | |||||
| chr1:1288772
|
G | A | 3 | a0002c0002t0001g0019a0002c0003t0002g0107a0007c0006t0001g0072 | 3 | HG01358.hp2 HG01361.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1662+735G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288772 | ||||||
| chr1:1288773
|
T | TCC | 19 | a0001c0001t0001g0215a0001c0001t0002g0227a0001c0001t0002g0233others(16): Show | 19 | HG00280.hp1 HG00544.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1662+738_1662+739d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288773 | |||||
| chr1:1288773
|
T | TCCCCCGT others(33): Show |
1 | a0002c0003t0002g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1662+739_1662+740i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288773 | |||||
| chr1:1288773
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1662+739_1662+740i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288773 | |||||
| chr1:1288773
|
T | TCCCGTGT others(46): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+749_1662+750i others(55): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288773 | |||||
| chr1:1288773
|
TCCCGTGT others(387): Show |
T | 1 | a0002c0028t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1662+765_1663-1076 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288773 | |||||
| chr1:1288775
|
CCGTGTCT others(49): Show |
C | 2 | a0001c0001t0001g0207a0003c0004t0003g0134 | 2 | HG03579.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1662+740_1662+795d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288775 | |||||
| chr1:1288775
|
CCGTGTCT others(179): Show |
C | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1662+740_1662+925d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288775 | |||||
| chr1:1288775
|
CCGTGTCT others(197): Show |
C | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1662+740_1662+943d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288775 | |||||
| chr1:1288777
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1662+740G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288777 | ||||||
| chr1:1288777
|
G | C | 1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+740G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288777 | ||||||
| chr1:1288778
|
T | A | 1 | a0003c0004t0003g0152 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1662+741T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288778 | ||||||
| chr1:1288778
|
T | C | 1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+741T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288778 | ||||||
| chr1:1288778
|
TGTCTCTG others(33): Show |
T | 4 | a0001c0012t0001g0131a0002c0002t0001g0059a0002c0002t0001g0085others(1): Show | 4 | HG01517.hp2 NA18747.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+758_1662+797d others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288778 | |||||
| chr1:1288779
|
GTCTCTGC others(447): Show |
G | 1 | a0006c0010t0007g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1662+746_1663-1035 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288779 | |||||
| chr1:1288781
|
C | G | 1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+744C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288781 | ||||||
| chr1:1288782
|
T | C | 18 | a0001c0001t0001g0166a0001c0001t0001g0185a0001c0001t0001g0186others(15): Show | 18 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1662+745T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288782 | ||||||
| chr1:1288787
|
T | C | 53 | a0001c0001t0001g0180a0001c0001t0001g0185a0001c0001t0001g0215others(50): Show | 53 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1662+750T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288787 | ||||||
| chr1:1288787
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288787 | |||||
| chr1:1288787
|
T | TCCGTCCC others(50): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(59): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288787 | |||||
| chr1:1288790
|
G | A | 1 | a0002c0003t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1662+753G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288790 | ||||||
| chr1:1288791
|
TCC | T | 66 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0178others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1662+758_1662+759d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288791 | |||||
| chr1:1288791
|
TCCCCCGT others(15): Show |
T | 1 | a0001c0001t0001g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1662+758_1662+779d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288791 | |||||
| chr1:1288791
|
TCCCCCGT others(295): Show |
T | 1 | a0001c0001t0002g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1662+758_1662+1059 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288791 | |||||
| chr1:1288791
|
TCCCCCGT others(389): Show |
T | 1 | a0002c0002t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1662+758_1663-1081 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288791 | |||||
| chr1:1288791
|
TCCCCCGT others(465): Show |
T | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1662+758_1663-1005 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288791 | |||||
| chr1:1288792
|
C | CCCGTGTC others(47): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288792 | |||||
| chr1:1288792
|
C | T | 1 | a0002c0003t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1662+755C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288792 | ||||||
| chr1:1288793
|
C | CCCCGTGT others(749): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1662+768_1662+769i others(758): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCCCGTGT others(11): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1662+764_1662+765i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCCCGTGT others(903): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1662+764_1662+765i others(912): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1662+764_1662+765i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCC others(65): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCC others(9): Show |
1 | a0023c0045t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCC others(27): Show |
2 | a0001c0001t0001g0177a0001c0001t0005g0258 | 2 | HG03654.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1662+757_1662+758i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(9): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(63): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(83): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(119): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(128): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(265): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(274): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(63): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(49): Show |
1 | a0002c0003t0004g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0217a0002c0003t0001g0026a0002c0003t0002g0122 | 3 | HG01934.hp1 HG02145.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1662+757_1662+758i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(29): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(49): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(135): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(144): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(101): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(83): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(65): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(431): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(440): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(267): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1662+757_1662+758i others(276): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
C | CCGTGTCT others(455): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+757_1662+758i others(464): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288793
|
CCCCGTGT others(311): Show |
C | 2 | a0003c0004t0003g0004a0003c0004t0003g0007 | 2 | NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1662+769_1662+1086 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288793 | |||||
| chr1:1288798
|
T | A | 4 | a0001c0001t0001g0196a0003c0004t0003g0143a0003c0004t0003g0148others(1): Show | 4 | HG01109.hp2 HG02896.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+761T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288798 | ||||||
| chr1:1288798
|
T | TGTCTCTG others(11): Show |
1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1662+764_1662+765i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288798 | |||||
| chr1:1288798
|
T | TGTCTCTG others(51): Show |
1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1662+764_1662+765i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288798 | |||||
| chr1:1288798
|
TGTCCCTG others(13): Show |
T | 2 | a0002c0002t0001g0003a0003c0004t0003g0152 | 2 | HG00438.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1662+765_1662+784d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288798 | |||||
| chr1:1288799
|
GTCCCTGT others(15): Show |
G | 3 | a0004c0008t0001g0239a0004c0008t0001g0240a0019c0026t0001g0014 | 3 | HG02258.hp1 HG02976.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1662+765_1662+786d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288799 | |||||
| chr1:1288799
|
GTCCCTGT others(1092): Show |
G | 1 | a0005c0011t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1662+765_1663-371d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288799 | |||||
| chr1:1288801
|
C | CTCTGCCC others(69): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+764_1662+765i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288801 | ||||||
| chr1:1288802
|
C | T | 171 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0179others(168): Show | 171 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1662+765C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288802 | ||||||
| chr1:1288802
|
CCTGTTCC others(13): Show |
C | 1 | a0006c0010t0007g0270 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1662+769_1662+788d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288802 | |||||
| chr1:1288806
|
T | C | 208 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0166others(205): Show | 208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1662+769T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288806 | ||||||
| chr1:1288807
|
T | C | 45 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0204others(42): Show | 45 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1662+770T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288807 | ||||||
| chr1:1288807
|
T | TCCGTCCC others(121): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1662+777_1662+778i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288807 | |||||
| chr1:1288809
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+772C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288809 | ||||||
| chr1:1288810
|
G | A | 2 | a0002c0003t0004g0116a0008c0007t0004g0285 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1662+773G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288810 | ||||||
| chr1:1288810
|
G | C | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1662+773G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288810 | ||||||
| chr1:1288811
|
TCC | T | 62 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0184others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1662+778_1662+779d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288811 | |||||
| chr1:1288811
|
TCCCCCGA others(125): Show |
T | 1 | a0003c0004t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1662+778_1662+909d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288811 | |||||
| chr1:1288812
|
C | G | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1662+775C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288812 | ||||||
| chr1:1288812
|
C | T | 2 | a0002c0003t0004g0116a0008c0007t0004g0285 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1662+775C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288812 | ||||||
| chr1:1288813
|
C | CCCCGTGT others(11): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1662+780_1662+781i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCC others(9): Show |
1 | a0002c0002t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(29): Show |
2 | a0002c0002t0001g0043a0002c0002t0001g0068 | 2 | HG04204.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1662+777_1662+778i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(179): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(188): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(45): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1662+777_1662+778i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(27): Show |
1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(83): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(244): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(253): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(83): Show |
3 | a0002c0003t0004g0111a0002c0003t0004g0119a0002c0003t0004g0120 | 3 | HG01884.hp1 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1662+777_1662+778i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(9): Show |
6 | a0001c0001t0001g0192a0001c0001t0001g0237a0001c0001t0002g0230others(3): Show | 6 | HG01891.hp1 HG01928.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+777_1662+778i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(220): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(229): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(29): Show |
1 | a0001c0001t0002g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1662+777_1662+778i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(177): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1662+777_1662+778i others(186): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(153): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(162): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(305): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(314): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(27): Show |
2 | a0001c0001t0001g0204a0007c0006t0001g0073 | 2 | HG01975.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1662+777_1662+778i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(195): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1662+777_1662+778i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1662+777_1662+778i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | CCGTGTCT others(7): Show |
1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1662+777_1662+778i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288813
|
C | T | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1662+776C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288813 | ||||||
| chr1:1288813
|
CCCCGAGT others(11): Show |
C | 2 | a0001c0001t0001g0160a0009c0014t0001g0050 | 2 | HG03688.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1662+781_1662+798d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288813 | |||||
| chr1:1288816
|
C | T | 1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1662+779C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288816 | ||||||
| chr1:1288818
|
A | T | 194 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0179others(191): Show | 194 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1662+781A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288818 | ||||||
| chr1:1288821
|
C | G | 3 | a0002c0002t0001g0017a0002c0003t0002g0027a0015c0037t0001g0090 | 3 | HG02293.hp1 HG04184.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1662+784C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288821 | ||||||
| chr1:1288822
|
T | C | 16 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0186others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+785T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288822 | ||||||
| chr1:1288822
|
T | TCTGCTCC others(200): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+797_1662+798i others(209): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288822 | |||||
| chr1:1288827
|
T | C | 41 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0192others(38): Show | 41 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1662+790T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288827 | ||||||
| chr1:1288830
|
G | A | 2 | a0007c0006t0001g0072a0008c0007t0004g0286 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1662+793G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288830 | ||||||
| chr1:1288831
|
T | TCC | 30 | a0001c0001t0001g0184a0001c0001t0001g0204a0001c0001t0001g0237others(27): Show | 30 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1662+796_1662+797d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288831 | |||||
| chr1:1288831
|
T | TCCCCCGT others(149): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1662+797_1662+798i others(158): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288831 | |||||
| chr1:1288831
|
T | TCCCCCGT others(167): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1662+797_1662+798i others(176): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288831 | |||||
| chr1:1288831
|
T | TCCCGTGT others(69): Show |
2 | a0002c0003t0002g0012a0020c0030t0002g0103 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1662+807_1662+808i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288831 | |||||
| chr1:1288834
|
C | T | 2 | a0008c0007t0004g0286a0009c0014t0001g0050 | 2 | HG03139.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1662+797C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288834 | ||||||
| chr1:1288835
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1662+798G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288835 | ||||||
| chr1:1288835
|
G | C | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+798G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288835 | ||||||
| chr1:1288836
|
T | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0207a0012c0022t0006g0269 | 3 | HG01975.hp2 HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1662+799T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288836 | ||||||
| chr1:1288836
|
T | C | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+799T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288836 | ||||||
| chr1:1288836
|
TGTCTCTG others(105): Show |
T | 1 | a0003c0004t0003g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1662+857_1662+968d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288836 | |||||
| chr1:1288839
|
C | G | 2 | a0002c0003t0001g0018a0005c0011t0001g0157 | 2 | HG02622.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1662+802C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288839 | ||||||
| chr1:1288840
|
T | C | 20 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0002g0232others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1662+803T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288840 | ||||||
| chr1:1288845
|
T | C | 53 | a0001c0001t0001g0162a0001c0001t0001g0187a0001c0001t0001g0192others(50): Show | 53 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1662+808T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288845 | ||||||
| chr1:1288845
|
T | TCCGTCCC others(67): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1662+820_1662+821i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288845 | |||||
| chr1:1288849
|
T | TCC | 41 | a0001c0001t0001g0162a0001c0001t0001g0201a0001c0001t0001g0202others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1662+814_1662+815d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCCCGT others(15): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+815_1662+816i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCCCGT others(369): Show |
1 | a0001c0001t0002g0230 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1662+815_1662+816i others(378): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCCCGT others(51): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1662+815_1662+816i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCCCGT others(127): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1662+815_1662+816i others(136): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCGTGT others(295): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1662+833_1662+834i others(304): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCGTGT others(49): Show |
1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1662+833_1662+834i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288849
|
T | TCCCGTGT others(31): Show |
1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1662+843_1662+844i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288849 | |||||
| chr1:1288851
|
CCGTGTCT others(9): Show |
C | 1 | a0002c0002t0001g0010 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1662+816_1662+831d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288851 | |||||
| chr1:1288851
|
CCGTGTCT others(121): Show |
C | 1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+816_1662+943d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288851 | |||||
| chr1:1288853
|
G | A | 1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1662+816G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288853 | ||||||
| chr1:1288853
|
G | C | 2 | a0001c0001t0001g0194a0019c0026t0001g0014 | 2 | HG01261.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1662+816G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288853 | ||||||
| chr1:1288854
|
T | A | 3 | a0001c0001t0002g0227a0003c0004t0003g0145a0025c0044t0003g0257 | 3 | HG00280.hp1 HG02559.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1662+817T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288854 | ||||||
| chr1:1288854
|
T | C | 2 | a0001c0001t0001g0194a0019c0026t0001g0014 | 2 | HG01261.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1662+817T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288854 | ||||||
| chr1:1288857
|
C | CCCTGCTC others(759): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+820_1662+821i others(768): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288857 | ||||||
| chr1:1288857
|
C | G | 2 | a0001c0001t0001g0194a0019c0026t0001g0014 | 2 | HG01261.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1662+820C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288857 | ||||||
| chr1:1288858
|
T | C | 23 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0214others(20): Show | 23 | HG00621.hp2 HG00738.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1662+821T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288858 | ||||||
| chr1:1288862
|
CTCCGTCC others(67): Show |
C | 1 | a0002c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1662+834_1662+907d others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288862 | |||||
| chr1:1288863
|
T | C | 49 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0201others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1662+826T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288863 | ||||||
| chr1:1288866
|
G | A | 3 | a0002c0002t0001g0019a0002c0002t0001g0076a0030c0024t0001g0051 | 3 | HG01358.hp2 NA18983.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1662+829G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288866 | ||||||
| chr1:1288867
|
T | TCC | 30 | a0001c0001t0001g0187a0001c0001t0001g0195a0001c0001t0001g0212others(27): Show | 30 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.1662+832_1662+833d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288867 | |||||
| chr1:1288867
|
T | TCCCCCGT others(105): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1662+833_1662+834i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288867 | |||||
| chr1:1288867
|
T | TCCCCCGT others(32): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1662+833_1662+834i others(41): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288867 | |||||
| chr1:1288867
|
T | TCCCCCGT others(111): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1662+833_1662+834i others(120): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288867 | |||||
| chr1:1288867
|
T | TCCCCCGT others(393): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1662+833_1662+834i others(402): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288867 | |||||
| chr1:1288867
|
T | TCCCGTGT others(583): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1662+851_1662+852i others(592): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288867 | |||||
| chr1:1288867
|
T | TTCCCCGT others(15): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1662+830_1662+831i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288867 | ||||||
| chr1:1288869
|
CCGTGTCT others(9): Show |
C | 3 | a0003c0004t0003g0133a0003c0004t0003g0135a0003c0004t0003g0153 | 3 | NA18964.hp2 NA18998.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1662+834_1662+849d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288869 | |||||
| chr1:1288869
|
CCGTGTCT others(329): Show |
C | 1 | a0002c0002t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1662+834_1663-1065 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288869 | |||||
| chr1:1288871
|
G | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0246a0002c0002t0001g0102 | 3 | HG02818.hp2 HG02922.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662+834G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288871 | ||||||
| chr1:1288872
|
T | A | 3 | a0001c0001t0002g0161a0004c0008t0001g0262a0023c0045t0001g0164 | 3 | HG02040.hp1 HG03579.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1662+835T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288872 | ||||||
| chr1:1288872
|
T | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0246a0002c0002t0001g0102 | 3 | HG02818.hp2 HG02922.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662+835T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288872 | ||||||
| chr1:1288872
|
TGTCTCTG others(69): Show |
T | 1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1662+857_1662+932d others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288872 | |||||
| chr1:1288875
|
C | G | 3 | a0001c0001t0001g0242a0001c0001t0001g0246a0002c0002t0001g0102 | 3 | HG02818.hp2 HG02922.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1662+838C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288875 | ||||||
| chr1:1288876
|
T | C | 18 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0198others(15): Show | 18 | HG00280.hp2 HG00738.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1662+839T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288876 | ||||||
| chr1:1288876
|
T | TCTGCTCC others(11): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1662+857_1662+874d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288876 | |||||
| chr1:1288876
|
T | TGCTCCGT others(9): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1662+839_1662+840i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288876 | ||||||
| chr1:1288876
|
TCTGCTCC others(11): Show |
T | 1 | a0018c0027t0001g0020 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1662+857_1662+874d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288876 | |||||
| chr1:1288881
|
T | C | 53 | a0001c0001t0001g0180a0001c0001t0001g0184a0001c0001t0001g0185others(50): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1662+844T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288881 | ||||||
| chr1:1288881
|
T | TCCGTCCC others(103): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1662+851_1662+852i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288881 | |||||
| chr1:1288881
|
T | TCCGTCCC others(161): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1662+856_1662+857i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288881 | |||||
| chr1:1288885
|
T | TCC | 42 | a0001c0001t0001g0178a0001c0001t0001g0189a0001c0001t0001g0198others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1662+850_1662+851d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288885 | |||||
| chr1:1288885
|
T | TCCCCCGT others(33): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662+851_1662+852i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288885 | |||||
| chr1:1288885
|
TCCCGTGT others(445): Show |
T | 1 | a0004c0005t0010g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1662+857_1663-926d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288885 | |||||
| chr1:1288889
|
G | C | 1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+852G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288889 | ||||||
| chr1:1288890
|
T | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0208a0006c0010t0007g0275 | 3 | HG00280.hp2 HG01433.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1662+853T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288890 | ||||||
| chr1:1288890
|
T | C | 1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+853T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288890 | ||||||
| chr1:1288890
|
TGTCCCTG others(51): Show |
T | 2 | a0002c0002t0001g0059a0009c0013t0001g0078 | 2 | NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1662+857_1662+914d others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288890 | |||||
| chr1:1288890
|
TGTCCCTG others(181): Show |
T | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1662+857_1662+1044 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288890 | |||||
| chr1:1288890
|
TGTCCCTG others(779): Show |
T | 1 | a0002c0003t0004g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1662+857_1663-592d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288890 | |||||
| chr1:1288893
|
C | G | 1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+856C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288893 | ||||||
| chr1:1288894
|
C | CCTGCCCC others(29): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1662+861_1662+862i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288894 | |||||
| chr1:1288894
|
C | CCTGCTCC others(359): Show |
1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1662+874_1662+875i others(368): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288894 | |||||
| chr1:1288894
|
C | T | 167 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0178others(164): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1662+857C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288894 | ||||||
| chr1:1288898
|
CTCCGTCC others(31): Show |
C | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1662+870_1662+907d others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288898 | |||||
| chr1:1288899
|
T | C | 51 | a0001c0001t0001g0167a0001c0001t0001g0189a0001c0001t0001g0201others(48): Show | 51 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1662+862T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288899 | ||||||
| chr1:1288899
|
T | TCCGTCCC others(191): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1662+874_1662+875i others(200): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288899 | |||||
| chr1:1288902
|
G | A | 1 | a0002c0002t0001g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1662+865G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288902 | ||||||
| chr1:1288903
|
T | TCC | 23 | a0001c0001t0001g0181a0001c0001t0001g0213a0001c0001t0002g0231others(20): Show | 23 | HG01069.hp1 HG01070.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1662+868_1662+869d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288903 | |||||
| chr1:1288903
|
T | TCCCCCGT others(71): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1662+869_1662+870i others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288903 | |||||
| chr1:1288903
|
TCCCGTGT others(447): Show |
T | 1 | a0002c0002t0001g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1662+888_1663-893d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288903 | |||||
| chr1:1288903
|
TCCCGTGT others(485): Show |
T | 1 | a0002c0002t0001g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1662+888_1663-855d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288903 | |||||
| chr1:1288908
|
T | A | 1 | a0003c0004t0003g0146 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1662+871T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288908 | ||||||
| chr1:1288908
|
TGTCTCTG others(33): Show |
T | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1662+888_1662+927d others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288908 | |||||
| chr1:1288912
|
T | C | 20 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0196others(17): Show | 20 | HG00597.hp2 HG01070.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1662+875T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288912 | ||||||
| chr1:1288916
|
CTCCGTCC others(34): Show |
C | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+880_1662+920d others(43): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288916 | ||||||
| chr1:1288917
|
T | C | 63 | a0001c0001t0001g0187a0001c0001t0001g0195a0001c0001t0001g0201others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1662+880T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288917 | ||||||
| chr1:1288917
|
T | TCCGTCCC others(85): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288917 | |||||
| chr1:1288917
|
T | TCCGTCCC others(51): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1662+887_1662+888i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288917 | |||||
| chr1:1288917
|
T | TCCGTCCC others(1591): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(1600): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288917 | |||||
| chr1:1288919
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1662+882C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288919 | ||||||
| chr1:1288920
|
G | A | 2 | a0002c0003t0004g0115a0030c0024t0001g0051 | 2 | HG02976.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1662+883G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288920 | ||||||
| chr1:1288921
|
TCC | T | 74 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0178others(71): Show | 74 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1662+888_1662+889d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288921 | |||||
| chr1:1288921
|
TCCCCCGT others(15): Show |
T | 5 | a0001c0012t0001g0131a0002c0002t0001g0003a0002c0002t0001g0013others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+888_1662+909d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288921 | |||||
| chr1:1288921
|
TCCCCCGT others(164): Show |
T | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1662+889_1662+1059 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288921 | |||||
| chr1:1288921
|
TCCCCCGT others(165): Show |
T | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1662+888_1662+1059 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288921 | |||||
| chr1:1288922
|
C | T | 2 | a0002c0003t0004g0115a0030c0024t0001g0051 | 2 | HG02976.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1662+885C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288922 | ||||||
| chr1:1288923
|
C | CCCCGTGT others(11): Show |
2 | a0001c0001t0001g0245a0002c0003t0002g0104 | 2 | HG01928.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1662+894_1662+895i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCCCGTGT others(49): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1662+894_1662+895i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCCCGTGT others(101): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1662+894_1662+895i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCCCGTGT others(47): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+894_1662+895i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCCCGTGT others(9): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1662+894_1662+895i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCCCGTGT others(120): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+894_1662+895i others(129): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCC others(47): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(29): Show |
1 | a0003c0004t0003g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(275): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(284): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(155): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1662+887_1662+888i others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(103): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(9): Show |
7 | a0001c0001t0001g0217a0001c0018t0001g0251a0002c0002t0001g0068others(4): Show | 7 | HG01934.hp1 HG02071.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662+887_1662+888i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(173): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(182): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(63): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(215): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1662+887_1662+888i others(224): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(27): Show |
1 | a0002c0003t0002g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1662+887_1662+888i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
C | CCGTGTCT others(63): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1662+887_1662+888i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288923
|
CCCCGTGT others(649): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1662+895_1663-684d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288923 | |||||
| chr1:1288928
|
T | A | 10 | a0001c0001t0001g0213a0001c0001t0002g0225a0001c0001t0002g0254others(7): Show | 10 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662+891T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288928 | ||||||
| chr1:1288928
|
T | TGTCTCTG others(29): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+894_1662+895i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288928 | |||||
| chr1:1288928
|
TGTCCCTG others(13): Show |
T | 6 | a0001c0001t0001g0175a0002c0003t0001g0069a0002c0003t0001g0091others(3): Show | 6 | HG01361.hp2 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+895_1662+914d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288928 | |||||
| chr1:1288930
|
TCC | T | 5 | a0002c0002t0001g0056a0002c0002t0001g0102a0002c0003t0001g0018others(2): Show | 5 | HG01109.hp1 HG02738.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+895_1662+896d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288930 | |||||
| chr1:1288932
|
C | T | 189 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0165others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1662+895C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288932 | ||||||
| chr1:1288932
|
CCTGTTCC others(13): Show |
C | 1 | a0002c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1662+899_1662+918d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288932 | |||||
| chr1:1288936
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(216): Show | 220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1662+899T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288936 | ||||||
| chr1:1288937
|
T | C | 52 | a0001c0001t0001g0160a0001c0001t0001g0201a0001c0001t0001g0202others(49): Show | 52 | HG00558.hp1 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1662+900T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288937 | ||||||
| chr1:1288937
|
T | TCCGTCCC others(49): Show |
1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288937 | |||||
| chr1:1288937
|
T | TCCGTCCC others(195): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288937 | |||||
| chr1:1288939
|
C | T | 3 | a0001c0001t0002g0161a0001c0046t0001g0259a0019c0026t0001g0014 | 3 | HG02040.hp1 HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1662+902C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288939 | ||||||
| chr1:1288940
|
G | A | 3 | a0002c0002t0001g0029a0008c0007t0004g0284a0008c0007t0004g0287 | 3 | HG00423.hp1 HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1662+903G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288940 | ||||||
| chr1:1288941
|
TCC | T | 77 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0177others(74): Show | 77 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1662+908_1662+909d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288941 | |||||
| chr1:1288941
|
TCCCCCGA others(87): Show |
T | 1 | a0006c0010t0007g0270 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1662+908_1662+1001 others(97): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288941 | |||||
| chr1:1288942
|
C | T | 3 | a0002c0002t0001g0029a0008c0007t0004g0284a0008c0007t0004g0287 | 3 | HG00423.hp1 HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1662+905C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288942 | ||||||
| chr1:1288943
|
C | CCCCGTGT others(347): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1662+910_1662+911i others(356): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCC others(307): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(316): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCC others(247): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1662+907_1662+908i others(256): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(9): Show |
1 | a0002c0003t0004g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(29): Show |
1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(139): Show |
1 | a0002c0002t0001g0030 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1662+907_1662+908i others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(81): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(85): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(269): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1662+907_1662+908i others(278): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(9): Show |
3 | a0002c0002t0001g0023a0003c0004t0003g0172a0005c0016t0001g0289 | 3 | HG02004.hp1 HG02165.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1662+907_1662+908i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(245): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1662+907_1662+908i others(254): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(65): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1662+907_1662+908i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(29): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(83): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1662+907_1662+908i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(273): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(282): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(191): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(200): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(159): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288943
|
C | CCGTGTCT others(123): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1662+907_1662+908i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288943 | |||||
| chr1:1288946
|
C | T | 3 | a0008c0007t0004g0284a0008c0007t0004g0287a0009c0014t0001g0050 | 3 | HG02109.hp2 HG03195.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1662+909C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288946 | ||||||
| chr1:1288948
|
A | T | 206 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0165others(203): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1662+911A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288948 | ||||||
| chr1:1288951
|
C | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0055a0002c0003t0002g0101 | 3 | HG03831.hp1 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1662+914C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288951 | ||||||
| chr1:1288952
|
T | C | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0246others(6): Show | 9 | HG01069.hp2 HG01070.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662+915T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288952 | ||||||
| chr1:1288957
|
T | C | 52 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0181others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+920T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288957 | ||||||
| chr1:1288960
|
G | A | 1 | a0002c0003t0004g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1662+923G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288960 | ||||||
| chr1:1288961
|
T | TCC | 38 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0189others(35): Show | 38 | HG00597.hp1 HG01081.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1662+926_1662+927d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288961 | |||||
| chr1:1288961
|
T | TCCCCCGT others(15): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1662+927_1662+928i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288961 | |||||
| chr1:1288961
|
T | TCCCCCGT others(69): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1662+927_1662+928i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288961 | |||||
| chr1:1288961
|
T | TCCCGTGT others(33): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1662+937_1662+938i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288961 | |||||
| chr1:1288961
|
T | TCCCGTGT others(51): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+937_1662+938i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288961 | |||||
| chr1:1288961
|
T | TCCCGTGT others(89): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1662+963_1662+964i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288961 | |||||
| chr1:1288965
|
G | A | 2 | a0001c0001t0001g0178a0004c0008t0001g0262 | 2 | HG01081.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1662+928G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288965 | ||||||
| chr1:1288965
|
G | C | 3 | a0002c0002t0001g0080a0003c0004t0003g0172a0027c0039t0002g0136 | 3 | HG02165.hp1 HG02523.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1662+928G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288965 | ||||||
| chr1:1288966
|
T | A | 1 | a0003c0004t0003g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1662+929T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288966 | ||||||
| chr1:1288966
|
T | C | 3 | a0002c0002t0001g0080a0003c0004t0003g0172a0027c0039t0002g0136 | 3 | HG02165.hp1 HG02523.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1662+929T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288966 | ||||||
| chr1:1288969
|
C | G | 3 | a0002c0002t0001g0080a0003c0004t0003g0172a0027c0039t0002g0136 | 3 | HG02165.hp1 HG02523.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1662+932C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288969 | ||||||
| chr1:1288970
|
T | C | 14 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0188others(11): Show | 14 | HG00099.hp2 HG01106.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662+933T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288970 | ||||||
| chr1:1288970
|
T | TGCTCCGT others(9): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1662+933_1662+934i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288970 | ||||||
| chr1:1288975
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0165others(53): Show | 57 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1662+938T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288975 | ||||||
| chr1:1288975
|
T | TCCGTCCC others(105): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1662+955_1662+956i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288975 | |||||
| chr1:1288977
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1662+940C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288977 | ||||||
| chr1:1288979
|
T | TCC | 30 | a0001c0001t0001g0175a0001c0001t0001g0213a0001c0001t0001g0216others(27): Show | 30 | HG00408.hp1 HG00544.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1662+944_1662+945d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288979 | |||||
| chr1:1288979
|
T | TCCCGTGT others(87): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1662+950_1662+951i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288979 | |||||
| chr1:1288979
|
T | TCCCGTGT others(67): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1662+955_1662+956i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288979 | |||||
| chr1:1288981
|
CCGTGTCT others(9): Show |
C | 1 | a0009c0013t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1662+946_1662+961d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288981 | |||||
| chr1:1288981
|
CCGTGTCT others(65): Show |
C | 1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1662+946_1662+1017 others(75): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288981 | |||||
| chr1:1288983
|
G | C | 2 | a0002c0002t0001g0088a0010c0019t0003g0170 | 2 | HG02155.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1662+946G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288983 | ||||||
| chr1:1288984
|
T | A | 4 | a0001c0001t0001g0175a0001c0001t0002g0260a0003c0004t0003g0138others(1): Show | 4 | HG01361.hp2 HG02523.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+947T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288984 | ||||||
| chr1:1288984
|
T | C | 2 | a0002c0002t0001g0088a0010c0019t0003g0170 | 2 | HG02155.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1662+947T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288984 | ||||||
| chr1:1288984
|
TGTCTCTG others(87): Show |
T | 1 | a0005c0011t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1662+964_1662+1057 others(97): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288984 | |||||
| chr1:1288987
|
C | G | 2 | a0002c0002t0001g0088a0010c0019t0003g0170 | 2 | HG02155.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1662+950C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288987 | ||||||
| chr1:1288988
|
T | C | 14 | a0001c0001t0001g0165a0001c0001t0001g0185a0001c0001t0001g0186others(11): Show | 14 | HG01123.hp1 HG01952.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662+951T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288988 | ||||||
| chr1:1288988
|
T | TCTGCCCC others(123): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1662+955_1662+956i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288988 | |||||
| chr1:1288988
|
TCTGCTCC others(996): Show |
T | 1 | a0012c0022t0006g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1662+969_1663-263d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288988 | |||||
| chr1:1288993
|
T | C | 57 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0181others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1662+956T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288993 | ||||||
| chr1:1288993
|
T | TCCGTCCC others(199): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1662+963_1662+964i others(208): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288993 | |||||
| chr1:1288995
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1662+958C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288995 | ||||||
| chr1:1288996
|
G | A | 1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1662+959G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1288996 | ||||||
| chr1:1288997
|
T | TCC | 29 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0001t0002g0140others(26): Show | 29 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1662+962_1662+963d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288997 | |||||
| chr1:1288997
|
T | TCCCCCGT others(91): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1662+963_1662+964i others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288997 | |||||
| chr1:1288997
|
T | TCCCCCGT others(53): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1662+963_1662+964i others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288997 | |||||
| chr1:1288997
|
T | TCCCGTGT others(49): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1662+973_1662+974i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288997 | |||||
| chr1:1288997
|
T | TCCCGTGT others(163): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1662+981_1662+982i others(172): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288997 | |||||
| chr1:1288999
|
CCGTGTCT others(9): Show |
C | 1 | a0002c0002t0001g0017 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1662+964_1662+979d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288999 | |||||
| chr1:1288999
|
CCGTGTCT others(47): Show |
C | 1 | a0002c0002t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1662+964_1662+1017 others(57): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288999 | |||||
| chr1:1288999
|
CCGTGTCT others(105): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1662+964_1662+1075 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1288999 | |||||
| chr1:1289001
|
G | C | 3 | a0001c0001t0001g0196a0002c0002t0001g0055a0004c0008t0001g0262 | 3 | HG03579.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1662+964G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289001 | ||||||
| chr1:1289002
|
T | C | 3 | a0001c0001t0001g0196a0002c0002t0001g0055a0004c0008t0001g0262 | 3 | HG03579.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1662+965T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289002 | ||||||
| chr1:1289002
|
TGTCTCTG others(31): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1662+987_1662+1024 others(41): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289002 | |||||
| chr1:1289005
|
C | CTCTGCTC others(11): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+981_1662+982i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289005 | |||||
| chr1:1289005
|
C | G | 3 | a0001c0001t0001g0196a0002c0002t0001g0055a0004c0008t0001g0262 | 3 | HG03579.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1662+968C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289005 | ||||||
| chr1:1289006
|
T | C | 17 | a0001c0001t0001g0175a0001c0001t0001g0193a0001c0001t0001g0208others(14): Show | 17 | HG00280.hp2 HG00597.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1662+969T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289006 | ||||||
| chr1:1289006
|
TCTGCTCC others(107): Show |
T | 1 | a0005c0011t0001g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1662+987_1662+1100 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289006 | |||||
| chr1:1289011
|
T | C | 54 | a0001c0001t0001g0160a0001c0001t0001g0168a0001c0001t0001g0178others(51): Show | 54 | HG00438.hp2 HG01070.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1662+974T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289011 | ||||||
| chr1:1289011
|
T | TCCGTCCC others(143): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1662+986_1662+987i others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289011 | |||||
| chr1:1289014
|
G | A | 1 | a0004c0008t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1662+977G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289014 | ||||||
| chr1:1289015
|
T | TCC | 39 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0197others(36): Show | 39 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1662+980_1662+981d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289015 | |||||
| chr1:1289015
|
T | TCCCCCGT others(91): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1662+981_1662+982i others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289015 | |||||
| chr1:1289015
|
T | TCCCCCGT others(33): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1662+981_1662+982i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289015 | |||||
| chr1:1289015
|
TCCCGTGT others(71): Show |
T | 1 | a0003c0004t0003g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1662+1000_1662+107 others(82): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289015 | |||||
| chr1:1289015
|
TCCCGTGT others(145): Show |
T | 1 | a0003c0004t0003g0005 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1662+987_1663-1096 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289015 | |||||
| chr1:1289015
|
TCCCGTGT others(373): Show |
T | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1662+987_1663-868d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289015 | |||||
| chr1:1289017
|
CCGTGTCC others(87): Show |
C | 2 | a0002c0002t0001g0011a0004c0008t0001g0239 | 2 | HG02258.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1662+982_1662+1075 others(97): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289017 | |||||
| chr1:1289019
|
G | A | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1662+982G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289019 | ||||||
| chr1:1289019
|
G | C | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+982G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289019 | ||||||
| chr1:1289020
|
T | A | 3 | a0001c0001t0001g0208a0002c0002t0001g0056a0002c0003t0002g0038 | 3 | HG00280.hp2 HG03239.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1662+983T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289020 | ||||||
| chr1:1289020
|
T | C | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+983T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289020 | ||||||
| chr1:1289023
|
C | G | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+986C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289023 | ||||||
| chr1:1289024
|
C | CCTGCTCC others(65): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(75): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289024 | |||||
| chr1:1289024
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(183): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1662+987C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289024 | ||||||
| chr1:1289024
|
CCTGCTCC others(13): Show |
C | 2 | a0002c0002t0001g0096a0003c0004t0003g0142 | 2 | HG00558.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1662+1000_1662+101 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289024 | |||||
| chr1:1289026
|
T | C | 1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1662+989T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289026 | ||||||
| chr1:1289029
|
T | C | 54 | a0001c0001t0001g0162a0001c0001t0001g0187a0001c0001t0001g0201others(51): Show | 54 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1662+992T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289029 | ||||||
| chr1:1289029
|
T | TCCGTCCC others(13): Show |
1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1662+1002_1662+100 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289029 | |||||
| chr1:1289029
|
T | TCCGTCCC others(11): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(21): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289029 | |||||
| chr1:1289029
|
T | TCCGTCCC others(109): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(119): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289029 | |||||
| chr1:1289032
|
G | A | 5 | a0001c0001t0001g0175a0002c0002t0001g0016a0003c0004t0003g0139others(2): Show | 5 | HG01175.hp2 HG01361.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+995G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289032 | ||||||
| chr1:1289033
|
TCC | T | 71 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0181others(68): Show | 71 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1662+1000_1662+100 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289033 | |||||
| chr1:1289033
|
TCCCCCGA others(33): Show |
T | 1 | a0002c0002t0001g0008 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1662+1000_1662+103 others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289033 | |||||
| chr1:1289033
|
TCCCCCGA others(53): Show |
T | 1 | a0002c0002t0013g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1662+1000_1662+105 others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289033 | |||||
| chr1:1289033
|
TCCCCCGA others(127): Show |
T | 1 | a0009c0013t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1662+1000_1663-110 others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289033 | |||||
| chr1:1289034
|
C | T | 4 | a0002c0002t0001g0016a0003c0004t0003g0139a0003c0004t0003g0253others(1): Show | 4 | HG01175.hp2 NA19056.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+997C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289034 | ||||||
| chr1:1289035
|
C | CCCCGTGT others(29): Show |
1 | a0004c0005t0010g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1662+1002_1662+100 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCCCGTGT others(65): Show |
1 | a0003c0004t0003g0171 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1662+1002_1662+100 others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCCCGTGT others(45): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1662+1002_1662+100 others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCC others(573): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(583): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCC others(117): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(127): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(9): Show |
2 | a0002c0003t0001g0097a0003c0004t0003g0145 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1662+999_1662+1000 others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(57): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(143): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(153): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(99): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(109): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(276): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(286): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(871): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(881): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(61): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(71): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(9): Show |
4 | a0001c0001t0001g0179a0001c0001t0002g0140a0001c0009t0001g0210others(1): Show | 4 | HG01255.hp1 HG01256.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+999_1662+1000 others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(199): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(209): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(29): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(39): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(55): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(305): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1662+999_1662+1000 others(315): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(37): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(175): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(185): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(45): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(55): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(45): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(55): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(45): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(55): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(117): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(127): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
C | CCGTGTCT others(299): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+999_1662+1000 others(309): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
CCCCGAGT others(11): Show |
C | 2 | a0003c0004t0003g0134a0010c0019t0003g0098 | 2 | HG02015.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1662+1003_1662+102 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
CCCCGAGT others(69): Show |
C | 2 | a0003c0004t0003g0006a0003c0004t0003g0106 | 2 | HG01346.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1662+1003_1662+107 others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
CCCCGAGT others(105): Show |
C | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1662+1003_1662+111 others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289035
|
CCCCGAGT others(163): Show |
C | 1 | a0002c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1662+1003_1663-106 others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289035 | |||||
| chr1:1289038
|
C | T | 3 | a0003c0004t0003g0139a0003c0004t0003g0253a0021c0032t0002g0039 | 3 | HG01175.hp2 NA19070.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1662+1001C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289038 | ||||||
| chr1:1289040
|
A | AGTCTCTG others(31): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1662+1019_1662+102 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289040 | |||||
| chr1:1289040
|
A | AGTCTCTG others(49): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1662+1019_1662+102 others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289040 | |||||
| chr1:1289040
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(205): Show | 209 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1662+1003A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289040 | ||||||
| chr1:1289043
|
C | CTCTGCTC others(9): Show |
1 | a0001c0001t0001g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1662+1010_1662+102 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289043 | |||||
| chr1:1289043
|
C | G | 2 | a0001c0001t0001g0245a0018c0027t0001g0020 | 2 | HG06807.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1662+1006C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289043 | ||||||
| chr1:1289044
|
T | C | 16 | a0001c0001t0001g0187a0001c0001t0001g0195a0001c0001t0001g0203others(13): Show | 16 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1662+1007T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289044 | ||||||
| chr1:1289044
|
T | TCTGCTCC others(125): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1662+1019_1662+102 others(136): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289044 | |||||
| chr1:1289044
|
T | TCTGCTCC others(211): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1662+1029_1662+103 others(222): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289044 | |||||
| chr1:1289049
|
T | C | 32 | a0001c0001t0001g0178a0001c0001t0001g0193a0001c0001t0001g0217others(29): Show | 32 | HG00099.hp2 HG00408.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1662+1012T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289049 | ||||||
| chr1:1289052
|
G | A | 3 | a0002c0002t0001g0042a0003c0004t0003g0144a0030c0024t0001g0051 | 3 | NA18970.hp1 NA18983.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1662+1015G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289052 | ||||||
| chr1:1289053
|
T | TCC | 14 | a0001c0001t0001g0187a0001c0001t0001g0198a0001c0001t0002g0173others(11): Show | 14 | HG00544.hp2 HG01257.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662+1018_1662+101 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289053 | |||||
| chr1:1289053
|
T | TCCCCCGT others(481): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1662+1019_1662+102 others(492): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289053 | |||||
| chr1:1289053
|
T | TCCCGTGT others(369): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1662+1029_1662+103 others(380): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289053 | |||||
| chr1:1289053
|
T | TTC | 3 | a0002c0002t0001g0042a0003c0004t0003g0144a0030c0024t0001g0051 | 3 | NA18970.hp1 NA18983.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1662+1016_1662+101 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289053 | ||||||
| chr1:1289053
|
TCCCGTGT others(107): Show |
T | 3 | a0002c0002t0001g0059a0003c0004t0003g0135a0003c0004t0003g0153 | 3 | NA18964.hp2 NA18969.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1662+1041_1663-108 others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289053 | |||||
| chr1:1289055
|
CCGTGTCT others(49): Show |
C | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1662+1020_1662+107 others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289055 | |||||
| chr1:1289055
|
CCGTGTCT others(67): Show |
C | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1662+1020_1662+109 others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289055 | |||||
| chr1:1289057
|
G | C | 1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1662+1020G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289057 | ||||||
| chr1:1289058
|
T | C | 1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1662+1021T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289058 | ||||||
| chr1:1289058
|
TGTCTCTG others(13): Show |
T | 1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1662+1041_1662+106 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289058 | |||||
| chr1:1289061
|
C | G | 1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1662+1024C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289061 | ||||||
| chr1:1289062
|
T | C | 11 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0001g0197others(8): Show | 11 | HG00558.hp1 HG01106.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+1025T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289062 | ||||||
| chr1:1289062
|
T | TCTGCTCC others(51): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289062 | |||||
| chr1:1289062
|
TCTGCTCC others(33): Show |
T | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1662+1038_1662+107 others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289062 | |||||
| chr1:1289062
|
TCTGCTCC others(51): Show |
T | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1662+1038_1662+109 others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289062 | |||||
| chr1:1289062
|
TCTGCTCC others(501): Show |
T | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1662+1038_1663-689 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289062 | |||||
| chr1:1289066
|
C | CTCCGTCC others(13): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1662+1040_1662+104 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289066 | |||||
| chr1:1289066
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1662+1029C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289066 | ||||||
| chr1:1289067
|
T | C | 52 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0201others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+1030T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289067 | ||||||
| chr1:1289067
|
T | TCCGTCCC others(31): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289067 | |||||
| chr1:1289067
|
T | TCCGTCCC others(71): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(82): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289067 | |||||
| chr1:1289067
|
T | TCCGTCCC others(369): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(380): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289067 | |||||
| chr1:1289067
|
TCCGTCCC others(69): Show |
T | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1662+1038_1662+111 others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289067 | |||||
| chr1:1289067
|
TCCGTCCC others(239): Show |
T | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1662+1038_1663-951 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289067 | |||||
| chr1:1289070
|
G | A | 3 | a0002c0003t0004g0114a0002c0003t0004g0121a0006c0010t0007g0270 | 3 | HG00738.hp1 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1662+1033G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289070 | ||||||
| chr1:1289071
|
TCC | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0175others(82): Show | 86 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1662+1038_1662+103 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289071 | |||||
| chr1:1289071
|
TCCCCCGA others(259): Show |
T | 1 | a0018c0027t0001g0020 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1662+1038_1663-931 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289071 | |||||
| chr1:1289071
|
TCCCCCGA others(279): Show |
T | 1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+1038_1663-911 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289071 | |||||
| chr1:1289072
|
C | T | 2 | a0002c0003t0004g0114a0002c0003t0004g0121 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1662+1035C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289072 | ||||||
| chr1:1289073
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+1040_1662+104 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCCCGTGT others(67): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1662+1040_1662+104 others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCCCGTGT others(105): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1662+1040_1662+104 others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCCCGTGT others(177): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1662+1040_1662+104 others(188): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCCCGTGT others(193): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1662+1040_1662+104 others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCC others(9): Show |
1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCC others(47): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCC others(65): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCC others(27): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCC others(139): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(150): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(9): Show |
2 | a0002c0003t0002g0024a0005c0016t0001g0281 | 2 | HG01069.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1662+1037_1662+103 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(83): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(29): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(27): Show |
1 | a0006c0010t0007g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(359): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(370): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(99): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(9): Show |
3 | a0002c0002t0001g0019a0002c0002t0001g0080a0002c0003t0002g0105 | 3 | HG01358.hp2 HG02523.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1662+1037_1662+103 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(329): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(340): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(368): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(379): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(137): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(27): Show |
1 | a0002c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(63): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(81): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(27): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(45): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(135): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
C | CCGTGTCT others(29): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1662+1037_1662+103 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
CCCCGAGT others(31): Show |
C | 2 | a0002c0002t0001g0089a0003c0004t0003g0146 | 2 | NA18969.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1662+1041_1662+107 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
CCCCGAGT others(125): Show |
C | 1 | a0002c0002t0001g0010 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1662+1041_1663-106 others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289073
|
CCCCGAGT others(201): Show |
C | 1 | a0002c0002t0001g0067 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1662+1041_1663-986 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289073 | |||||
| chr1:1289077
|
G | C | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+1040G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289077 | ||||||
| chr1:1289078
|
A | AGTCTCTG others(309): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1662+1049_1662+105 others(320): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289078 | |||||
| chr1:1289078
|
A | C | 1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1662+1041A>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289078 | ||||||
| chr1:1289078
|
A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1662+1041A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289078 | ||||||
| chr1:1289081
|
C | G | 2 | a0001c0018t0001g0251a0002c0003t0001g0018 | 2 | HG02071.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1662+1044C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289081 | ||||||
| chr1:1289082
|
T | C | 17 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0177others(14): Show | 17 | HG00741.hp1 HG01106.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1662+1045T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289082 | ||||||
| chr1:1289082
|
T | TGCTCCGT others(9): Show |
2 | a0001c0001t0001g0243a0002c0002t0001g0045 | 2 | HG02451.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1662+1045_1662+104 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289082 | ||||||
| chr1:1289087
|
T | C | 52 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0178others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+1050T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289087 | ||||||
| chr1:1289087
|
T | TCCGTCCC others(11): Show |
1 | a0002c0002t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289087 | |||||
| chr1:1289087
|
T | TCCGTCCC others(49): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289087 | |||||
| chr1:1289091
|
TCC | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0165a0001c0001t0001g0167others(82): Show | 86 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1662+1058_1662+105 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289091 | |||||
| chr1:1289091
|
TCCCCCGT others(297): Show |
T | 1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1662+1058_1663-873 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289091 | |||||
| chr1:1289093
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1662+1064_1662+106 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCCCGTGT others(65): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1662+1064_1662+106 others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCCCGTGT others(9): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662+1064_1662+106 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCCCGTGT others(81): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1662+1064_1662+106 others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCC others(9): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(9): Show |
5 | a0002c0003t0004g0114a0002c0003t0004g0120a0002c0003t0004g0121others(2): Show | 5 | HG02109.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+1057_1662+105 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(29): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(85): Show |
1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(63): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(9): Show |
2 | a0001c0001t0001g0179a0001c0001t0011g0267 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1662+1057_1662+105 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(1169): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(1180): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(423): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(434): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(123): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(27): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(85): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(153): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
C | CCGTGTCT others(83): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1662+1057_1662+105 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
CCCCGTGT others(11): Show |
C | 1 | a0003c0004t0003g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1662+1083_1662+110 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
CCCCGTGT others(29): Show |
C | 1 | a0001c0001t0002g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1662+1065_1662+110 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289093
|
CCCCGTGT others(47): Show |
C | 1 | a0008c0007t0004g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1662+1078_1663-110 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289093 | |||||
| chr1:1289098
|
T | A | 2 | a0001c0001t0001g0192a0003c0004t0003g0143 | 2 | HG01109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1662+1061T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289098 | ||||||
| chr1:1289100
|
TCC | T | 8 | a0001c0001t0001g0246a0002c0002t0001g0046a0002c0003t0001g0097others(5): Show | 8 | HG02015.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1662+1065_1662+106 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289100 | |||||
| chr1:1289100
|
TCCCTGCT others(49): Show |
T | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1662+1065_1663-111 others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289100 | |||||
| chr1:1289102
|
C | T | 162 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0175others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1662+1065C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289102 | ||||||
| chr1:1289107
|
T | C | 49 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0214others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1662+1070T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289107 | ||||||
| chr1:1289110
|
G | A | 1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1662+1073G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289110 | ||||||
| chr1:1289111
|
T | TCC | 42 | a0001c0001t0001g0177a0001c0001t0001g0196a0001c0001t0001g0197others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1662+1076_1662+107 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289111 | |||||
| chr1:1289111
|
T | TCCCCCGT others(51): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1662+1077_1662+107 others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289111 | |||||
| chr1:1289111
|
T | TCCCGTGT others(351): Show |
1 | a0020c0030t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1662+1082_1662+108 others(362): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289111 | |||||
| chr1:1289111
|
T | TCCCGTGT others(350): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1662+1082_1662+108 others(361): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289111 | |||||
| chr1:1289113
|
CCGTGTCC others(9): Show |
C | 3 | a0003c0004t0003g0133a0003c0004t0003g0143a0004c0005t0006g0128 | 3 | HG01109.hp2 HG02895.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1662+1078_1662+109 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289113 | |||||
| chr1:1289113
|
CCGTGTCC others(27): Show |
C | 1 | a0003c0004t0003g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1662+1078_1662+111 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289113 | |||||
| chr1:1289120
|
C | CCTGCTCC others(47): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1662+1100_1662+110 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289120 | |||||
| chr1:1289120
|
C | CCTGCTCC others(173): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1662+1105_1662+110 others(184): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289120 | |||||
| chr1:1289120
|
C | T | 172 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0166others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1662+1083C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289120 | ||||||
| chr1:1289120
|
CCTGCTCC others(69): Show |
C | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1662+1106_1663-105 others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289120 | |||||
| chr1:1289122
|
T | C | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1662+1085T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289122 | ||||||
| chr1:1289125
|
T | C | 52 | a0001c0001t0001g0177a0001c0001t0001g0200a0001c0001t0001g0201others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+1088T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289125 | ||||||
| chr1:1289125
|
T | TCCGTCCC others(87): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1663-1116_1663-111 others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289125 | |||||
| chr1:1289128
|
G | A | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1662+1091G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289128 | ||||||
| chr1:1289128
|
G | C | 2 | a0002c0002t0001g0076a0002c0002t0001g0088 | 2 | NA18973.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1662+1091G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289128 | ||||||
| chr1:1289129
|
T | TCC | 32 | a0001c0001t0001g0184a0001c0001t0001g0208a0001c0001t0002g0161others(29): Show | 32 | HG00280.hp2 HG01175.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1662+1094_1662+109 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289129 | |||||
| chr1:1289129
|
T | TCCCCCGT others(307): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1662+1095_1662+109 others(318): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289129 | |||||
| chr1:1289129
|
T | TCCCCCGT others(15): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1662+1095_1662+109 others(26): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289129 | |||||
| chr1:1289129
|
TCCCGTGT others(51): Show |
T | 2 | a0001c0001t0001g0242a0002c0002t0001g0016 | 2 | HG02922.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1662+1106_1663-107 others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289129 | |||||
| chr1:1289131
|
CCGTGTCT others(9): Show |
C | 3 | a0001c0001t0001g0191a0002c0002t0001g0037a0002c0002t0001g0053 | 3 | HG00099.hp1 NA18964.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1662+1096_1662+111 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289131 | |||||
| chr1:1289132
|
C | T | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1662+1095C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289132 | ||||||
| chr1:1289133
|
G | A | 1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1662+1096G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289133 | ||||||
| chr1:1289133
|
G | C | 4 | a0001c0001t0002g0227a0001c0018t0001g0251a0002c0002t0001g0055others(1): Show | 4 | HG00280.hp1 HG02071.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+1096G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289133 | ||||||
| chr1:1289134
|
T | A | 2 | a0001c0009t0001g0218a0023c0045t0001g0164 | 2 | HG02300.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1662+1097T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289134 | ||||||
| chr1:1289134
|
T | C | 3 | a0001c0001t0002g0227a0002c0002t0001g0055a0002c0002t0001g0080 | 3 | HG00280.hp1 HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1662+1097T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289134 | ||||||
| chr1:1289137
|
C | G | 3 | a0001c0018t0001g0251a0002c0002t0001g0055a0002c0002t0001g0080 | 3 | HG02071.hp1 HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1662+1100C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289137 | ||||||
| chr1:1289138
|
T | C | 21 | a0001c0001t0001g0168a0001c0001t0001g0179a0001c0001t0001g0192others(18): Show | 21 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1662+1101T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289138 | ||||||
| chr1:1289138
|
TCTGCCCC others(11): Show |
T | 4 | a0001c0001t0001g0185a0003c0004t0003g0004a0003c0004t0003g0006others(1): Show | 4 | HG01346.hp1 HG02738.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+1106_1663-111 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289138 | |||||
| chr1:1289140
|
T | C | 1 | a0002c0002t0001g0042 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1662+1103T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289140 | ||||||
| chr1:1289143
|
C | CCCGTCCC others(271): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1662+1113_1662+111 others(282): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289143 | |||||
| chr1:1289143
|
C | CCCGTCCC others(565): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662+1113_1662+111 others(576): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289143 | |||||
| chr1:1289143
|
C | CCCGTCCC others(139): Show |
1 | a0002c0003t0004g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663-1116_1663-111 others(150): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289143 | |||||
| chr1:1289143
|
C | T | 133 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(130): Show | 133 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.1662+1106C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289143 | ||||||
| chr1:1289143
|
CCCGTCCC others(11): Show |
C | 1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1662+1114_1663-110 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289143 | |||||
| chr1:1289143
|
CCCGTCCC others(31): Show |
C | 1 | a0003c0004t0003g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1662+1114_1663-108 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289143 | |||||
| chr1:1289146
|
G | A | 2 | a0002c0002t0001g0042a0004c0005t0010g0124 | 2 | HG03209.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1662+1109G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289146 | ||||||
| chr1:1289147
|
T | TCC | 25 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0001g0204others(22): Show | 25 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1662+1112_1662+111 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289147 | |||||
| chr1:1289147
|
T | TCCCCCGT others(33): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1662+1113_1662+111 others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289147 | |||||
| chr1:1289147
|
T | TCCCCCGT others(31): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1662+1113_1662+111 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289147 | |||||
| chr1:1289147
|
T | TCCCGTGT others(185): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1663-1116_1663-111 others(196): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289147 | |||||
| chr1:1289147
|
TCCCGTGT others(183): Show |
T | 1 | a0003c0004t0003g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1663-1115_1663-926 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289147 | |||||
| chr1:1289149
|
CCGTGTCC others(49): Show |
C | 1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1662+1114_1663-106 others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289149 | |||||
| chr1:1289149
|
CCGTGTCC others(125): Show |
C | 1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1662+1114_1663-989 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289149 | |||||
| chr1:1289150
|
C | T | 2 | a0002c0002t0001g0042a0004c0005t0010g0124 | 2 | HG03209.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1662+1113C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289150 | ||||||
| chr1:1289151
|
G | A | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1662+1114G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289151 | ||||||
| chr1:1289152
|
T | A | 1 | a0003c0004t0003g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1662+1115T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289152 | ||||||
| chr1:1289155
|
C | CTCTGCTC others(255): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-1116_1663-111 others(266): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289155 | ||||||
| chr1:1289156
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(173): Show | 177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1663-1115C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289156 | ||||||
| chr1:1289161
|
T | C | 56 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0186others(53): Show | 56 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1663-1110T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289161 | ||||||
| chr1:1289161
|
T | TCCGTCCC others(11): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289161 | |||||
| chr1:1289161
|
TCCGTCCC others(127): Show |
T | 1 | a0003c0004t0003g0146 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1663-1102_1663-969 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289161 | |||||
| chr1:1289163
|
C | T | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663-1108C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289163 | ||||||
| chr1:1289164
|
G | A | 2 | a0002c0002t0001g0041a0002c0002t0001g0043 | 2 | HG04204.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1663-1107G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289164 | ||||||
| chr1:1289165
|
TCC | T | 78 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0168others(75): Show | 78 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1663-1102_1663-110 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289165 | |||||
| chr1:1289165
|
TCCCCCGT others(15): Show |
T | 1 | a0001c0001t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1663-1102_1663-108 others(26): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289165 | |||||
| chr1:1289165
|
TCCCCCGT others(53): Show |
T | 1 | a0019c0026t0001g0014 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1663-1102_1663-104 others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289165 | |||||
| chr1:1289165
|
TCCCCCGT others(91): Show |
T | 1 | a0003c0004t0003g0133 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1663-1102_1663-100 others(102): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289165 | |||||
| chr1:1289166
|
C | T | 2 | a0002c0002t0001g0041a0002c0002t0001g0043 | 2 | HG04204.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1663-1105C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289166 | ||||||
| chr1:1289167
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1663-1096_1663-109 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCCCGTGT others(249): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(260): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCCCGTGT others(27): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-1095_1663-109 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(9): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(229): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(240): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(9): Show |
1 | a0003c0004t0003g0145 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(335): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(346): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(27): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(139): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(150): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCC others(227): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(238): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(9): Show |
2 | a0001c0009t0001g0205a0002c0002t0001g0033 | 2 | HG01257.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1663-1103_1663-110 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(67): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(63): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(196): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(207): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(121): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(9): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(209): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(220): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(27): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(283): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(294): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289167
|
C | CCGTGTCT others(117): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-1103_1663-110 others(128): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289167 | |||||
| chr1:1289170
|
C | T | 2 | a0001c0001t0002g0225a0004c0005t0010g0124 | 2 | HG01516.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1663-1101C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289170 | ||||||
| chr1:1289172
|
T | A | 10 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0198others(7): Show | 10 | HG00099.hp1 HG00544.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-1099T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289172 | ||||||
| chr1:1289175
|
C | CTCTGCTC others(11): Show |
1 | a0001c0001t0001g0178 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1663-1092_1663-107 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289175 | |||||
| chr1:1289176
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0187a0001c0001t0001g0197others(10): Show | 14 | HG01256.hp2 HG01258.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-1095T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289176 | ||||||
| chr1:1289176
|
T | TCTGCTCC others(281): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(292): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289176 | |||||
| chr1:1289176
|
T | TCTGCTCC others(345): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(356): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289176 | |||||
| chr1:1289181
|
T | C | 56 | a0001c0001t0001g0188a0001c0001t0001g0200a0001c0001t0001g0208others(53): Show | 56 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1663-1090T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289181 | ||||||
| chr1:1289181
|
T | TCCGTCCC others(103): Show |
1 | a0001c0001t0005g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289181 | |||||
| chr1:1289181
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0002g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289181 | |||||
| chr1:1289181
|
T | TCCGTCCC others(191): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(202): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289181 | |||||
| chr1:1289181
|
T | TCCGTCCC others(397): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(408): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289181 | |||||
| chr1:1289183
|
C | T | 3 | a0003c0004t0003g0004a0003c0004t0003g0006a0003c0004t0003g0007 | 3 | HG01346.hp1 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1663-1088C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289183 | ||||||
| chr1:1289184
|
G | A | 1 | a0004c0008t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1663-1087G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289184 | ||||||
| chr1:1289185
|
TCC | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0166others(90): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1663-1082_1663-108 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289185 | |||||
| chr1:1289187
|
C | CCCCGTGT others(371): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1663-1063_1663-106 others(382): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCCCGTGT others(159): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-1063_1663-106 others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCCCGTGT others(29): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1663-1063_1663-106 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCCCGTGT others(9): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-1075_1663-107 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCC others(9): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(9): Show |
1 | a0023c0045t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(47): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(63): Show |
1 | a0003c0004t0003g0152 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(9): Show |
5 | a0001c0001t0001g0215a0001c0001t0002g0140a0001c0009t0001g0210others(2): Show | 5 | HG01256.hp1 HG04184.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-1083_1663-108 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(175): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(186): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(193): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(83): Show |
1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(217): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(228): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289187
|
C | CCGTGTCT others(7): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1663-1083_1663-108 others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289187 | |||||
| chr1:1289192
|
T | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0002g0232 | 3 | HG01106.hp1 HG02132.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1663-1079T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289192 | ||||||
| chr1:1289196
|
T | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0197a0001c0001t0001g0243others(9): Show | 12 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1663-1075T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289196 | ||||||
| chr1:1289201
|
T | C | 51 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0175others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.1663-1070T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289201 | ||||||
| chr1:1289201
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-1053_1663-105 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289201 | |||||
| chr1:1289203
|
C | T | 1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-1068C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289203 | ||||||
| chr1:1289204
|
G | A | 1 | a0002c0002t0001g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1663-1067G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289204 | ||||||
| chr1:1289205
|
T | TCC | 16 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0212others(13): Show | 16 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-1064_1663-106 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289205 | |||||
| chr1:1289205
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1663-1063_1663-106 others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289205 | |||||
| chr1:1289205
|
T | TCCCCCGT others(13): Show |
1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1663-1063_1663-106 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289205 | |||||
| chr1:1289205
|
T | TCCCGTGT others(13): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663-1053_1663-105 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289205 | |||||
| chr1:1289205
|
T | TCCCGTGT others(31): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289205 | |||||
| chr1:1289207
|
C | T | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1663-1064C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289207 | ||||||
| chr1:1289207
|
CCGTGTCT others(67): Show |
C | 1 | a0002c0002t0001g0077 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1663-1062_1663-989 others(77): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289207 | |||||
| chr1:1289207
|
CCGTGTCT others(161): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1663-1062_1663-895 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289207 | |||||
| chr1:1289210
|
T | A | 1 | a0003c0004t0003g0151 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1663-1061T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289210 | ||||||
| chr1:1289213
|
C | CTCTGCCC others(47): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1663-1053_1663-105 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289213 | |||||
| chr1:1289214
|
T | C | 11 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0191others(8): Show | 11 | HG00099.hp1 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1663-1057T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289214 | ||||||
| chr1:1289214
|
TCTGCTCC others(313): Show |
T | 1 | a0002c0002t0001g0076 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1663-1044_1663-725 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289214 | |||||
| chr1:1289219
|
T | C | 64 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0178others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1663-1052T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289219 | ||||||
| chr1:1289219
|
T | TCCGTCCC others(509): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(520): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289219 | |||||
| chr1:1289219
|
T | TCCGTCCC others(351): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(362): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289219 | |||||
| chr1:1289219
|
TCCGTCCC others(69): Show |
T | 1 | a0002c0002t0001g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1663-1044_1663-969 others(79): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289219 | |||||
| chr1:1289221
|
C | T | 1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1663-1050C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289221 | ||||||
| chr1:1289222
|
G | A | 3 | a0002c0002t0001g0035a0002c0002t0001g0047a0002c0002t0001g0108 | 3 | HG01952.hp1 HG03704.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1663-1049G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289222 | ||||||
| chr1:1289223
|
TCC | T | 83 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0177others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1663-1044_1663-104 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289223 | |||||
| chr1:1289223
|
TCCCCCGT others(127): Show |
T | 1 | a0003c0004t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1663-1044_1663-911 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289223 | |||||
| chr1:1289224
|
C | CCCGTGTC others(47): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289224 | |||||
| chr1:1289224
|
C | T | 3 | a0002c0002t0001g0035a0002c0002t0001g0047a0002c0002t0001g0108 | 3 | HG01952.hp1 HG03704.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1663-1047C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289224 | ||||||
| chr1:1289225
|
C | CCCCGTGT others(29): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1663-1037_1663-103 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCCCGTGT others(45): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-1037_1663-103 others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCC others(63): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(69): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(47): Show |
1 | a0004c0005t0010g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(67): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(1323): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(1334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(123): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0001g0202 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(9): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(83): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(143): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(154): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(29): Show |
2 | a0001c0001t0001g0245a0001c0001t0011g0267 | 2 | HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1663-1045_1663-104 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(27): Show |
1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(47): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(83): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289225
|
C | CCGTGTCT others(291): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-1045_1663-104 others(302): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289225 | |||||
| chr1:1289229
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1663-1042G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289229 | ||||||
| chr1:1289230
|
T | A | 3 | a0001c0001t0001g0192a0003c0004t0003g0141a0006c0010t0007g0275 | 3 | HG03540.hp1 NA19067.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1663-1041T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289230 | ||||||
| chr1:1289231
|
GTC | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0168a0002c0002t0001g0102 | 3 | HG01106.hp1 NA18947.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1663-1036_1663-103 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289231 | |||||
| chr1:1289234
|
T | C | 16 | a0001c0001t0001g0166a0001c0001t0001g0178a0001c0001t0001g0189others(13): Show | 16 | HG00099.hp1 HG00738.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-1037T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289234 | ||||||
| chr1:1289234
|
T | TCTGCCCC others(127): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1663-1033_1663-103 others(138): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289234 | |||||
| chr1:1289234
|
T | TCTGCTCC others(123): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-1025_1663-102 others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289234 | |||||
| chr1:1289234
|
TCTGCTCC others(49): Show |
T | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1663-1032_1663-977 others(59): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289234 | |||||
| chr1:1289234
|
TCTGCTCC others(85): Show |
T | 1 | a0003c0004t0003g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1663-1024_1663-933 others(95): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289234 | |||||
| chr1:1289239
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0180others(44): Show | 48 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1663-1032T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289239 | ||||||
| chr1:1289239
|
TCCGTCCC others(49): Show |
T | 1 | a0002c0002t0013g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1663-1014_1663-959 others(59): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289239 | |||||
| chr1:1289241
|
C | T | 1 | a0003c0004t0003g0005 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1663-1030C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289241 | ||||||
| chr1:1289242
|
G | A | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1663-1029G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289242 | ||||||
| chr1:1289243
|
T | TCC | 25 | a0001c0001t0001g0179a0001c0001t0001g0184a0001c0001t0002g0233others(22): Show | 25 | HG00639.hp1 HG00673.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.1663-1026_1663-102 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
T | TCCCCCGT others(87): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1663-1025_1663-102 others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
T | TCCCCCGT others(375): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-1025_1663-102 others(386): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
T | TCCCGTGT others(31): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1663-1015_1663-101 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
T | TCCCGTGT others(13): Show |
1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1663-1019_1663-100 others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
T | TCCCGTGT others(89): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
T | TCCCGTGT others(31): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289243
|
TCCCGTGT others(87): Show |
T | 1 | a0002c0002t0001g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1663-999_1663-906d others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289243 | |||||
| chr1:1289245
|
CCGTGTCT others(29): Show |
C | 1 | a0002c0002t0001g0058 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1663-1024_1663-989 others(39): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289245 | |||||
| chr1:1289245
|
CCGTGTCT others(65): Show |
C | 2 | a0001c0001t0002g0228a0002c0002t0001g0017 | 2 | NA18612.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1663-1024_1663-953 others(75): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289245 | |||||
| chr1:1289249
|
GTC | G | 3 | a0001c0001t0001g0162a0001c0018t0001g0251a0002c0003t0001g0091 | 3 | HG00735.hp1 HG02071.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1663-1018_1663-101 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289249 | |||||
| chr1:1289251
|
CTCTGCTC others(257): Show |
C | 1 | a0002c0002t0001g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1663-1006_1663-743 others(3): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289251 | |||||
| chr1:1289252
|
T | C | 9 | a0001c0001t0001g0160a0001c0001t0001g0192a0001c0001t0001g0196others(6): Show | 9 | HG01069.hp1 HG01496.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1663-1019T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289252 | ||||||
| chr1:1289252
|
TCTGCTCC others(31): Show |
T | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1663-1014_1663-977 others(41): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289252 | |||||
| chr1:1289257
|
T | C | 55 | a0001c0001t0001g0179a0001c0001t0001g0193a0001c0001t0001g0196others(52): Show | 55 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1663-1014T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289257 | ||||||
| chr1:1289257
|
T | TCCGTCCC others(165): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-1000_1663-999 others(175): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289257 | |||||
| chr1:1289257
|
TCCGTCCC others(31): Show |
T | 2 | a0001c0001t0001g0175a0003c0004t0003g0005 | 2 | HG01361.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1663-1006_1663-969 others(41): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289257 | |||||
| chr1:1289257
|
TCCGTCCC others(49): Show |
T | 4 | a0003c0004t0003g0004a0003c0004t0003g0006a0003c0004t0003g0007others(1): Show | 4 | HG01346.hp1 NA18961.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-1006_1663-951 others(59): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289257 | |||||
| chr1:1289260
|
G | A | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1663-1011G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289260 | ||||||
| chr1:1289261
|
TCC | T | 75 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0168others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1663-1006_1663-100 others(6): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289261 | |||||
| chr1:1289261
|
TCCCCCGT others(69): Show |
T | 4 | a0001c0001t0002g0229a0004c0008t0001g0239a0005c0011t0001g0156others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-1006_1663-931 others(79): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289261 | |||||
| chr1:1289261
|
TCCCCCGT others(89): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1663-1006_1663-911 others(99): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289261 | |||||
| chr1:1289262
|
C | T | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1663-1009C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289262 | ||||||
| chr1:1289262
|
CCCCCGTG others(48): Show |
C | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1663-1005_1663-951 others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289262 | |||||
| chr1:1289263
|
C | CCCCGAGT others(107): Show |
1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1663-1004_1663-100 others(118): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCCCGAGT others(11): Show |
1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-1004_1663-100 others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCCCGAGT others(83): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1663-1004_1663-100 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCCCGTGT others(321): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663-1000_1663-999 others(331): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCCCGTGT others(351): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1663-1000_1663-999 others(361): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(9): Show |
1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(9): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(1171): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(1182): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(45): Show |
1 | a0006c0010t0007g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(281): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(292): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(103): Show |
1 | a0003c0004t0003g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCC others(63): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(9): Show |
1 | a0010c0019t0003g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(89): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(63): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(153): Show |
1 | a0002c0003t0004g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(121): Show |
1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0252a0002c0002t0001g0029a0002c0003t0001g0063 | 3 | HG00423.hp1 NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1663-1007_1663-100 others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(29): Show |
1 | a0002c0003t0004g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(49): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(199): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(210): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(85): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(45): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(141): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(27): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(83): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(27): Show |
2 | a0001c0009t0001g0211a0010c0019t0003g0170 | 2 | HG00639.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1663-1007_1663-100 others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
C | CCGTGTCT others(99): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1663-1007_1663-100 others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289263
|
CCCCGTGT others(11): Show |
C | 1 | a0003c0004t0003g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1663-994_1663-977d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289263 | |||||
| chr1:1289266
|
C | T | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1663-1005C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289266 | ||||||
| chr1:1289267
|
G | A | 2 | a0001c0001t0002g0140a0004c0005t0006g0126 | 2 | HG02258.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1663-1004G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289267 | ||||||
| chr1:1289268
|
T | A | 2 | a0001c0001t0002g0254a0007c0006t0001g0071 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1663-1003T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289268 | ||||||
| chr1:1289270
|
TCC | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0243a0001c0046t0001g0259others(2): Show | 5 | HG02165.hp1 HG02451.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-999_1663-998d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289270 | |||||
| chr1:1289272
|
C | CCTGCTCC others(13): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-987_1663-986i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289272 | |||||
| chr1:1289272
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0165a0001c0001t0001g0166others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1663-999C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289272 | ||||||
| chr1:1289276
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1663-995C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289276 | ||||||
| chr1:1289277
|
T | C | 51 | a0001c0001t0001g0166a0001c0001t0001g0178a0001c0001t0001g0184others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1663-994T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289277 | ||||||
| chr1:1289277
|
TCCGTCCC others(11): Show |
T | 1 | a0002c0002t0001g0037 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1663-981_1663-964d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289277 | |||||
| chr1:1289278
|
C | G | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1663-993C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289278 | ||||||
| chr1:1289279
|
C | T | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1663-992C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289279 | ||||||
| chr1:1289281
|
T | TCC | 35 | a0001c0001t0001g0165a0001c0001t0001g0189a0001c0001t0001g0190others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1663-988_1663-987d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289281 | |||||
| chr1:1289281
|
T | TCCCCCGT others(49): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-987_1663-986i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289281 | |||||
| chr1:1289281
|
T | TCCCCCGT others(69): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1663-987_1663-986i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289281 | |||||
| chr1:1289281
|
T | TCCCGTGT others(177): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1663-982_1663-981i others(186): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289281 | |||||
| chr1:1289281
|
TCCCGTGT others(69): Show |
T | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1663-981_1663-906d others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289281 | |||||
| chr1:1289283
|
CCGTGTCC others(9): Show |
C | 2 | a0002c0003t0002g0107a0003c0004t0003g0152 | 2 | HG01361.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1663-986_1663-971d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289283 | |||||
| chr1:1289283
|
CCGTGTCC others(325): Show |
C | 1 | a0002c0002t0001g0010 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1663-986_1663-655d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289283 | |||||
| chr1:1289286
|
T | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0198a0001c0001t0001g0208 | 3 | HG00280.hp2 HG01433.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1663-985T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289286 | ||||||
| chr1:1289289
|
C | CTCTGCTC others(11): Show |
2 | a0001c0001t0001g0250a0002c0002t0001g0046 | 2 | HG02015.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1663-982_1663-981i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289289 | ||||||
| chr1:1289290
|
C | CCTGCTCC others(925): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1663-977_1663-976i others(934): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289290 | |||||
| chr1:1289290
|
C | T | 187 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0166others(184): Show | 187 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1663-981C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289290 | ||||||
| chr1:1289295
|
C | CCCGTCCC others(89): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-969_1663-968i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289295 | |||||
| chr1:1289295
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1663-976C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289295 | ||||||
| chr1:1289298
|
G | A | 2 | a0002c0002t0001g0108a0026c0041t0001g0261 | 2 | HG03704.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1663-973G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289298 | ||||||
| chr1:1289299
|
T | TCC | 32 | a0001c0001t0001g0165a0001c0001t0001g0196a0001c0001t0001g0245others(29): Show | 32 | HG00408.hp1 HG00558.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1663-970_1663-969d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCCCGT others(185): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1663-969_1663-968i others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCCCGT others(65): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-969_1663-968i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCGTGT others(13): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1663-964_1663-963i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCGTGT others(13): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-959_1663-958i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCGTGT others(659): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1663-959_1663-958i others(668): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCGTGT others(69): Show |
1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1663-959_1663-958i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCGTGT others(161): Show |
1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1663-959_1663-958i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
T | TCCCGTGT others(31): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1663-959_1663-958i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289299
|
TCCCGTGT others(31): Show |
T | 1 | a0002c0002t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1663-958_1663-921d others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289299 | |||||
| chr1:1289301
|
CCGTGTCT others(9): Show |
C | 2 | a0003c0004t0003g0148a0014c0021t0008g0271 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1663-968_1663-953d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289301 | |||||
| chr1:1289303
|
G | C | 1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-968G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289303 | ||||||
| chr1:1289304
|
T | A | 2 | a0001c0001t0002g0254a0003c0004t0003g0152 | 2 | HG03195.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1663-967T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289304 | ||||||
| chr1:1289304
|
T | C | 1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-967T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289304 | ||||||
| chr1:1289307
|
C | G | 1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-964C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289307 | ||||||
| chr1:1289308
|
T | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0179a0001c0001t0001g0180others(16): Show | 20 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-963T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289308 | ||||||
| chr1:1289313
|
C | CCCGTCCC others(13): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1663-951_1663-950i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289313 | |||||
| chr1:1289313
|
C | CCCGTCCC others(29): Show |
1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1663-946_1663-945i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289313 | |||||
| chr1:1289313
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0167others(126): Show | 130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1663-958C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289313 | ||||||
| chr1:1289313
|
CCCGTCCC others(11): Show |
C | 5 | a0002c0002t0001g0013a0002c0002t0001g0016a0002c0002t0001g0025others(2): Show | 5 | HG01943.hp1 NA18960.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-950_1663-933d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289313 | |||||
| chr1:1289313
|
CCCGTCCC others(802): Show |
C | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1663-950_1663-142d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289313 | |||||
| chr1:1289315
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-956C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289315 | ||||||
| chr1:1289316
|
G | A | 2 | a0002c0003t0002g0083a0004c0008t0001g0241 | 2 | HG01109.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1663-955G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289316 | ||||||
| chr1:1289316
|
G | C | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1663-955G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289316 | ||||||
| chr1:1289317
|
T | TCC | 32 | a0001c0001t0001g0208a0001c0001t0001g0214a0001c0001t0002g0163others(29): Show | 32 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1663-952_1663-951d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289317 | |||||
| chr1:1289317
|
T | TCCCCCGT others(93): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1663-951_1663-950i others(102): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289317 | |||||
| chr1:1289317
|
T | TCCCCCGT others(381): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-951_1663-950i others(390): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289317 | |||||
| chr1:1289317
|
TCCCGTGT others(12): Show |
T | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1663-950_1663-932d others(21): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289317 | |||||
| chr1:1289317
|
TCCCGTGT others(33): Show |
T | 1 | a0001c0001t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1663-945_1663-906d others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289317 | |||||
| chr1:1289321
|
G | C | 1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-950G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289321 | ||||||
| chr1:1289322
|
T | A | 3 | a0001c0012t0001g0130a0002c0003t0002g0122a0003c0004t0003g0155 | 3 | HG02135.hp1 HG04184.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1663-949T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289322 | ||||||
| chr1:1289322
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-949T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289322 | ||||||
| chr1:1289325
|
C | G | 1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-946C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289325 | ||||||
| chr1:1289326
|
C | CCTGCTCC others(69): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289326 | |||||
| chr1:1289326
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1663-945C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289326 | ||||||
| chr1:1289330
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1663-941C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289330 | ||||||
| chr1:1289331
|
T | C | 67 | a0001c0001t0001g0160a0001c0001t0001g0196a0001c0001t0001g0197others(64): Show | 67 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1663-940T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289331 | ||||||
| chr1:1289333
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-938C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289333 | ||||||
| chr1:1289334
|
G | A | 5 | a0002c0002t0001g0029a0002c0002t0001g0053a0003c0004t0003g0220others(2): Show | 5 | HG00423.hp1 HG02132.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-937G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289334 | ||||||
| chr1:1289335
|
TCC | T | 74 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0168others(71): Show | 74 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1663-932_1663-931d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289335 | |||||
| chr1:1289335
|
TCCCCCGT others(15): Show |
T | 2 | a0001c0001t0001g0189a0002c0002t0001g0086 | 2 | HG02004.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1663-932_1663-911d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289335 | |||||
| chr1:1289336
|
C | T | 4 | a0002c0002t0001g0029a0002c0002t0001g0053a0004c0008t0001g0247others(1): Show | 4 | HG00423.hp1 HG03139.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-935C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289336 | ||||||
| chr1:1289337
|
C | CCCCGTGT others(185): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-921_1663-920i others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCCCGTGT others(547): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(556): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCCCGTGT others(47): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCC others(9): Show |
2 | a0001c0001t0001g0198a0002c0002t0001g0102 | 2 | HG01433.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1663-933_1663-932i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCC others(49): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCC others(65): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCC others(63): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(9): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(455): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(464): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(1098): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(1107): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(289): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(298): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(121): Show |
2 | a0002c0003t0002g0099a0020c0030t0002g0103 | 2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1663-933_1663-932i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(120): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(129): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(217): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(226): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(9): Show |
2 | a0001c0001t0001g0213a0001c0001t0002g0232 | 2 | HG02132.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1663-933_1663-932i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(119): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(128): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(87): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(615): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(624): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(83): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(63): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(101): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(173): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(182): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(1342): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(1351): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(102): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1663-933_1663-932i others(111): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289337
|
C | CCGTGTCT others(285): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-933_1663-932i others(294): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289337 | |||||
| chr1:1289342
|
T | A | 12 | a0001c0001t0001g0192a0001c0001t0001g0208a0003c0004t0003g0106others(9): Show | 12 | HG00280.hp2 HG00558.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.1663-929T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289342 | ||||||
| chr1:1289345
|
C | G | 1 | a0024c0033t0009g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1663-926C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289345 | ||||||
| chr1:1289346
|
T | C | 10 | a0001c0001t0001g0178a0001c0001t0001g0196a0001c0001t0001g0201others(7): Show | 10 | HG01069.hp2 HG01081.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1663-925T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289346 | ||||||
| chr1:1289351
|
T | C | 62 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0186others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1663-920T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289351 | ||||||
| chr1:1289351
|
T | TCCGTCCC others(49): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289351 | |||||
| chr1:1289353
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1663-918C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289353 | ||||||
| chr1:1289354
|
G | A | 2 | a0002c0002t0001g0037a0002c0002t0001g0041 | 2 | NA18947.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1663-917G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289354 | ||||||
| chr1:1289355
|
TCC | T | 78 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0166others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1663-912_1663-911d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289355 | |||||
| chr1:1289356
|
C | T | 2 | a0002c0002t0001g0037a0002c0002t0001g0041 | 2 | NA18947.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1663-915C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289356 | ||||||
| chr1:1289357
|
C | CCCCGTGT others(87): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1663-901_1663-900i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCCCGTGT others(951): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1663-901_1663-900i others(960): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCCCGTGT others(11): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1663-892_1663-875d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCCCGTGT others(103): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1663-875_1663-874i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCCCGTGT others(137): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-905_1663-904i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCC others(9): Show |
1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(9): Show |
4 | a0001c0001t0001g0165a0001c0001t0001g0193a0002c0003t0004g0120others(1): Show | 4 | HG02109.hp2 HG02293.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-913_1663-912i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(85): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(227): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(236): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(171): Show |
1 | a0002c0003t0004g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(180): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(9): Show |
3 | a0005c0016t0001g0289a0009c0014t0001g0009a0030c0024t0001g0051 | 3 | NA18946.hp2 NA18983.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1663-913_1663-912i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(29): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(103): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(453): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(462): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(287): Show |
1 | a0003c0004t0003g0171 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(296): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(155): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(281): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(290): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(27): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1663-913_1663-912i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(47): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(65): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(409): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(418): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(63): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289357
|
C | CCGTGTCT others(7): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-913_1663-912i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289357 | |||||
| chr1:1289361
|
G | A | 1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1663-910G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289361 | ||||||
| chr1:1289362
|
T | A | 5 | a0001c0001t0001g0178a0003c0004t0003g0004a0003c0004t0003g0006others(2): Show | 5 | HG01081.hp1 HG01346.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-909T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289362 | ||||||
| chr1:1289365
|
C | G | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1663-906C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289365 | ||||||
| chr1:1289366
|
T | C | 10 | a0001c0001t0001g0179a0001c0001t0001g0189a0001c0001t0001g0192others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-905T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289366 | ||||||
| chr1:1289366
|
T | TCTGCCCC others(51): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-901_1663-900i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289366 | |||||
| chr1:1289366
|
T | TCTGCTCC others(199): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1663-855_1663-854i others(208): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289366 | |||||
| chr1:1289371
|
T | C | 46 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0184others(43): Show | 46 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1663-900T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289371 | ||||||
| chr1:1289374
|
G | A | 1 | a0001c0012t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1663-897G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289374 | ||||||
| chr1:1289375
|
T | TCC | 24 | a0001c0001t0001g0162a0001c0001t0001g0190a0001c0001t0001g0213others(21): Show | 24 | HG00408.hp1 HG00544.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1663-894_1663-893d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289375 | |||||
| chr1:1289375
|
T | TCCCCCGT others(285): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-893_1663-892i others(294): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289375 | |||||
| chr1:1289375
|
T | TCCCCCGT others(51): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1663-893_1663-892i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289375 | |||||
| chr1:1289375
|
TCCCGTGT others(13): Show |
T | 2 | a0002c0002t0001g0059a0004c0008t0001g0239 | 2 | HG02258.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1663-874_1663-855d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289375 | |||||
| chr1:1289375
|
TCCCGTGT others(89): Show |
T | 1 | a0006c0010t0007g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1663-874_1663-779d others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289375 | |||||
| chr1:1289377
|
CCGTGTCT others(141): Show |
C | 1 | a0004c0005t0006g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1663-892_1663-745d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289377 | |||||
| chr1:1289379
|
G | A | 1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1663-892G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289379 | ||||||
| chr1:1289379
|
G | C | 2 | a0001c0001t0002g0260a0009c0014t0001g0050 | 2 | HG02523.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1663-892G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289379 | ||||||
| chr1:1289380
|
T | A | 1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1663-891T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289380 | ||||||
| chr1:1289380
|
T | C | 2 | a0001c0001t0002g0260a0009c0014t0001g0050 | 2 | HG02523.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1663-891T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289380 | ||||||
| chr1:1289383
|
C | G | 2 | a0001c0001t0002g0260a0009c0014t0001g0050 | 2 | HG02523.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1663-888C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289383 | ||||||
| chr1:1289384
|
T | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0192a0002c0002t0001g0017others(2): Show | 5 | HG01361.hp2 HG03239.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-887T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289384 | ||||||
| chr1:1289384
|
T | TCTGCTCC others(51): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1663-875_1663-874i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289384 | |||||
| chr1:1289389
|
T | C | 61 | a0001c0001t0001g0162a0001c0001t0001g0177a0001c0001t0001g0185others(58): Show | 61 | HG00558.hp1 HG00558.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1663-882T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289389 | ||||||
| chr1:1289391
|
C | T | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663-880C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289391 | ||||||
| chr1:1289392
|
G | A | 2 | a0002c0002t0001g0013a0002c0002t0001g0089 | 2 | HG01943.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1663-879G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289392 | ||||||
| chr1:1289393
|
TCC | T | 98 | a0001c0001t0001g0160a0001c0001t0001g0168a0001c0001t0001g0178others(95): Show | 98 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1663-874_1663-873d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289393 | |||||
| chr1:1289394
|
C | T | 2 | a0002c0002t0001g0013a0002c0002t0001g0089 | 2 | HG01943.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1663-877C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289394 | ||||||
| chr1:1289395
|
C | CCCCGTGT others(314): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-863_1663-862i others(323): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1663-854_1663-837d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCCCGTGT others(49): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1663-845_1663-844i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCCCGTGT others(65): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCC others(67): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCC others(45): Show |
1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0002g0249a0002c0003t0001g0110a0002c0003t0004g0121 | 3 | HG00597.hp1 HG02809.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1663-875_1663-874i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(29): Show |
1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1663-875_1663-874i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(793): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(802): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(47): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(101): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0180a0003c0004t0003g0172a0028c0038t0003g0283 | 3 | HG00639.hp2 HG01891.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1663-875_1663-874i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(29): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(201): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(210): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(81): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
C | CCGTGTCT others(27): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-875_1663-874i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289395
|
CCCCGTGT others(87): Show |
C | 1 | a0016c0031t0001g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1663-854_1663-761d others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289395 | |||||
| chr1:1289398
|
C | T | 1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1663-873C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289398 | ||||||
| chr1:1289400
|
T | A | 6 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0193others(3): Show | 6 | HG01192.hp2 HG01361.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-871T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289400 | ||||||
| chr1:1289400
|
T | TGTCTCTG others(49): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1663-845_1663-844i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289400 | |||||
| chr1:1289403
|
C | G | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1663-868C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289403 | ||||||
| chr1:1289404
|
T | C | 9 | a0001c0001t0001g0192a0001c0001t0001g0201a0002c0002t0001g0056others(6): Show | 9 | HG00673.hp1 HG01069.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663-867T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289404 | ||||||
| chr1:1289404
|
T | TCTGCCCC others(159): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-863_1663-862i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289404 | |||||
| chr1:1289404
|
T | TCTGCCCC others(65): Show |
1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1663-863_1663-862i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289404 | |||||
| chr1:1289404
|
T | TCTGCTCC others(11): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-850_1663-849i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289404 | |||||
| chr1:1289409
|
T | C | 62 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0188others(59): Show | 62 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1663-862T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289409 | ||||||
| chr1:1289409
|
T | TCCGTCCC others(11): Show |
5 | a0002c0003t0001g0069a0002c0003t0002g0012a0002c0003t0002g0024others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-845_1663-844i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289409 | |||||
| chr1:1289413
|
T | TCC | 21 | a0001c0001t0001g0165a0001c0001t0001g0190a0001c0001t0001g0217others(18): Show | 21 | HG00408.hp2 HG01243.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.1663-856_1663-855d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289413
|
T | TCCCCCGT others(67): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-855_1663-854i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289413
|
T | TCCCGTGT others(69): Show |
1 | a0001c0001t0005g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1663-850_1663-849i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289413
|
T | TCCCGTGT others(105): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1663-845_1663-844i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289413
|
T | TCCCGTGT others(142): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1663-845_1663-844i others(151): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289413
|
T | TCCCGTGT others(13): Show |
1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1663-836_1663-817d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289413
|
TCCCGTGT others(13): Show |
T | 1 | a0004c0008t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1663-836_1663-817d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289413 | |||||
| chr1:1289415
|
CCGTGTCT others(121): Show |
C | 1 | a0005c0011t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1663-854_1663-727d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289415 | |||||
| chr1:1289417
|
G | C | 2 | a0001c0001t0002g0260a0002c0002t0001g0045 | 2 | HG02523.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1663-854G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289417 | ||||||
| chr1:1289418
|
T | C | 2 | a0001c0001t0002g0260a0002c0002t0001g0045 | 2 | HG02523.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1663-853T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289418 | ||||||
| chr1:1289418
|
T | TGTCTCTG others(169): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-845_1663-844i others(178): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289418 | |||||
| chr1:1289421
|
C | G | 2 | a0001c0001t0002g0260a0002c0002t0001g0045 | 2 | HG02523.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1663-850C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289421 | ||||||
| chr1:1289422
|
T | C | 15 | a0001c0001t0001g0175a0001c0001t0001g0191a0001c0001t0001g0215others(12): Show | 15 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663-849T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289422 | ||||||
| chr1:1289422
|
TCTGCTCC others(123): Show |
T | 1 | a0002c0002t0001g0079 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1663-836_1663-707d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289422 | |||||
| chr1:1289423
|
C | A | 1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1663-848C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289423 | ||||||
| chr1:1289427
|
T | C | 59 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0179others(56): Show | 59 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1663-844T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289427 | ||||||
| chr1:1289427
|
T | TCCGTCCC others(51): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289427 | |||||
| chr1:1289427
|
T | TCCGTCCC others(529): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(538): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289427 | |||||
| chr1:1289427
|
T | TCCGTCCC others(1367): Show |
1 | a0001c0001t0002g0230 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(1376): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289427 | |||||
| chr1:1289429
|
C | T | 1 | a0002c0002t0001g0037 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1663-842C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289429 | ||||||
| chr1:1289430
|
G | A | 7 | a0002c0002t0001g0013a0002c0002t0001g0029a0002c0002t0001g0036others(4): Show | 7 | HG00408.hp2 HG00423.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-841G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289430 | ||||||
| chr1:1289431
|
TCC | T | 89 | a0001c0001t0001g0160a0001c0001t0001g0168a0001c0001t0001g0175others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1663-836_1663-835d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289431 | |||||
| chr1:1289432
|
C | T | 6 | a0002c0002t0001g0029a0002c0002t0001g0036a0002c0002t0001g0042others(3): Show | 6 | HG00408.hp2 HG00423.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-839C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289432 | ||||||
| chr1:1289433
|
C | CCCCGTGT others(11): Show |
2 | a0001c0001t0002g0173a0007c0006t0001g0072 | 2 | HG01993.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1663-825_1663-824i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCCCGTGT others(49): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-825_1663-824i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCCCGTGT others(11): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1663-825_1663-824i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCCCGTGT others(49): Show |
1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1663-807_1663-806i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCCCGTGT others(485): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1663-807_1663-806i others(494): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(9): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(9): Show |
2 | a0001c0020t0001g0263a0002c0002t0001g0049 | 2 | HG01952.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1663-837_1663-836i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(29): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(69): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(161): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(369): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(378): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(85): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(121): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(65): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(83): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(81): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(155): Show |
1 | a0008c0007t0004g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(65): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289433
|
C | CCGTGTCT others(191): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663-837_1663-836i others(200): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289433 | |||||
| chr1:1289434
|
C | CGTGTCTC others(4): Show |
1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1663-837_1663-836i others(13): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289434 | ||||||
| chr1:1289437
|
G | A | 1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1663-834G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289437 | ||||||
| chr1:1289438
|
T | A | 3 | a0001c0001t0001g0222a0001c0001t0011g0268a0001c0012t0001g0130 | 3 | HG01106.hp2 HG03225.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1663-833T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289438 | ||||||
| chr1:1289439
|
GTC | G | 3 | a0001c0001t0001g0207a0003c0004t0003g0139a0018c0027t0001g0020 | 3 | HG03579.hp1 NA18980.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1663-828_1663-827d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289439 | |||||
| chr1:1289441
|
C | G | 2 | a0004c0005t0010g0125a0025c0044t0003g0257 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-830C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289441 | ||||||
| chr1:1289442
|
T | C | 21 | a0001c0001t0001g0188a0001c0001t0001g0191a0001c0001t0001g0195others(18): Show | 21 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1663-829T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289442 | ||||||
| chr1:1289447
|
T | C | 49 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0189others(46): Show | 49 | HG00741.hp1 HG01069.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1663-824T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289447 | ||||||
| chr1:1289447
|
T | CCCGTCCC others(1865): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1663-825_1663-824i others(1874): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289447 | ||||||
| chr1:1289450
|
G | A | 4 | a0001c0001t0001g0175a0002c0002t0001g0035a0002c0003t0002g0083others(1): Show | 4 | HG00597.hp2 HG01361.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-821G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289450 | ||||||
| chr1:1289451
|
T | TCC | 20 | a0001c0001t0001g0217a0001c0001t0002g0225a0001c0001t0002g0228others(17): Show | 20 | HG00639.hp1 HG01069.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-818_1663-817d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289451
|
T | TCCCCCGT others(653): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1663-817_1663-816i others(662): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289451
|
T | TCCCGTGT others(331): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(340): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289451
|
T | TCCCGTGT others(31): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1663-807_1663-806i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289451
|
T | TCCCGTGT others(127): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1663-807_1663-806i others(136): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289451
|
T | TCCCGTGT others(67): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1663-807_1663-806i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289451
|
T | TCCCGTGT others(29): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-807_1663-806i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289451 | |||||
| chr1:1289452
|
C | T | 1 | a0002c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1663-819C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289452 | ||||||
| chr1:1289453
|
CCGTGTCT others(65): Show |
C | 1 | a0002c0002t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1663-816_1663-745d others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289453 | |||||
| chr1:1289453
|
CCGTGTCT others(83): Show |
C | 1 | a0002c0002t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1663-816_1663-727d others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289453 | |||||
| chr1:1289453
|
CCGTGTCT others(119): Show |
C | 2 | a0002c0002t0001g0037a0019c0026t0001g0014 | 2 | HG03490.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1663-816_1663-691d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289453 | |||||
| chr1:1289453
|
CCGTGTCT others(137): Show |
C | 1 | a0001c0001t0002g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1663-816_1663-673d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289453 | |||||
| chr1:1289453
|
CCGTGTCT others(155): Show |
C | 1 | a0002c0002t0001g0065 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1663-816_1663-655d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289453 | |||||
| chr1:1289453
|
CCGTGTCT others(229): Show |
C | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1663-816_1663-581d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289453 | |||||
| chr1:1289458
|
TCTCTGCC others(87): Show |
T | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1663-810_1663-717d others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289458 | |||||
| chr1:1289458
|
TCTCTGCC others(526): Show |
T | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1663-810_1663-278d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289458 | |||||
| chr1:1289459
|
CTCTGCCC others(506): Show |
C | 1 | a0018c0027t0001g0020 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1663-806_1663-294d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289459 | |||||
| chr1:1289460
|
T | C | 11 | a0001c0001t0001g0178a0001c0001t0001g0192a0001c0001t0001g0196others(8): Show | 11 | HG00438.hp1 HG01081.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1663-811T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289460 | ||||||
| chr1:1289460
|
TCTGCCCC others(67): Show |
T | 1 | a0002c0002t0001g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1663-806_1663-733d others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289460 | |||||
| chr1:1289460
|
TCTGCCCC others(85): Show |
T | 4 | a0001c0001t0001g0168a0003c0004t0003g0004a0003c0004t0003g0006others(1): Show | 4 | HG01106.hp1 HG01346.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-806_1663-715d others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289460 | |||||
| chr1:1289465
|
C | CCCGTCCC others(29): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289465 | |||||
| chr1:1289465
|
C | T | 122 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(119): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1663-806C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289465 | ||||||
| chr1:1289468
|
G | A | 11 | a0002c0002t0001g0011a0002c0002t0001g0013a0002c0002t0001g0025others(8): Show | 11 | HG00423.hp2 HG01243.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1663-803G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289468 | ||||||
| chr1:1289469
|
TCC | T | 65 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0177others(62): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1663-798_1663-797d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289469 | |||||
| chr1:1289469
|
TCCCCCGT others(378): Show |
T | 1 | a0004c0005t0010g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1663-798_1663-414d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289469 | |||||
| chr1:1289470
|
C | T | 11 | a0002c0002t0001g0011a0002c0002t0001g0013a0002c0002t0001g0025others(8): Show | 11 | HG00423.hp2 HG01243.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1663-801C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289470 | ||||||
| chr1:1289471
|
C | CCCCGTGT others(31): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1663-787_1663-786i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCCCGTGT others(415): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-787_1663-786i others(424): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCCCGTGT others(559): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-787_1663-786i others(568): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCCCGTGT others(171): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-791_1663-790i others(180): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCC others(9): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCC others(65): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(9): Show |
1 | a0002c0003t0004g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-799_1663-798i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(195): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-799_1663-798i others(204): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(265): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(274): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(27): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-799_1663-798i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(137): Show |
1 | a0001c0001t0001g0202 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(9): Show |
2 | a0001c0001t0001g0238a0002c0002t0001g0056 | 2 | HG02717.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1663-799_1663-798i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(364): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(373): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
C | CCGTGTCT others(427): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-799_1663-798i others(436): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
CCCCGTGT others(101): Show |
C | 2 | a0002c0002t0001g0013a0002c0002t0001g0089 | 2 | HG01943.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1663-760_1663-653d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289471
|
CCCCGTGT others(119): Show |
C | 1 | a0002c0002t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1663-760_1663-635d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289471 | |||||
| chr1:1289472
|
C | CCCGTGTC others(46): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1663-769_1663-768i others(55): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289472 | |||||
| chr1:1289475
|
G | A | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1663-796G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289475 | ||||||
| chr1:1289476
|
T | A | 5 | a0001c0001t0001g0245a0001c0001t0002g0254a0001c0012t0001g0131others(2): Show | 5 | HG01517.hp2 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-795T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289476 | ||||||
| chr1:1289479
|
C | CTCTGCTC others(67): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-761_1663-760i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289479 | |||||
| chr1:1289480
|
T | C | 14 | a0001c0001t0001g0166a0001c0001t0001g0178a0001c0001t0001g0179others(11): Show | 14 | HG00621.hp2 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-791T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289480 | ||||||
| chr1:1289480
|
T | TGCTCCGT others(27): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-791_1663-790i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289480 | ||||||
| chr1:1289480
|
TCTGCTCC others(83): Show |
T | 3 | a0001c0001t0002g0228a0002c0002t0001g0059a0009c0014t0001g0050 | 3 | HG03688.hp1 NA18969.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1663-760_1663-671d others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289480 | |||||
| chr1:1289484
|
CTCCGTCC others(356): Show |
C | 1 | a0002c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1663-778_1663-416d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289484 | |||||
| chr1:1289485
|
T | C | 51 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0195others(48): Show | 51 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1663-786T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289485 | ||||||
| chr1:1289485
|
T | TCCGTCCC others(109): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1663-779_1663-778i others(118): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289485 | |||||
| chr1:1289485
|
T | TCCGTCCC others(11): Show |
1 | a0002c0003t0002g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1663-769_1663-768i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289485 | |||||
| chr1:1289487
|
C | T | 1 | a0006c0010t0007g0270 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1663-784C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289487 | ||||||
| chr1:1289488
|
G | A | 1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-783G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289488 | ||||||
| chr1:1289489
|
T | TCC | 33 | a0001c0001t0001g0190a0001c0001t0001g0204a0001c0001t0001g0208others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.1663-780_1663-779d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289489 | |||||
| chr1:1289489
|
T | TCCCCCGT others(33): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-779_1663-778i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289489 | |||||
| chr1:1289489
|
T | TCCCCCGT others(51): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1663-779_1663-778i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289489 | |||||
| chr1:1289489
|
T | TCCCGTGT others(323): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-761_1663-760i others(332): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289489 | |||||
| chr1:1289491
|
CCGTGTCT others(81): Show |
C | 1 | a0003c0004t0003g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1663-778_1663-691d others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289491 | |||||
| chr1:1289491
|
CCGTGTCT others(99): Show |
C | 1 | a0002c0002t0001g0003 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1663-778_1663-673d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289491 | |||||
| chr1:1289491
|
CCGTGTCT others(135): Show |
C | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1663-778_1663-637d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289491 | |||||
| chr1:1289493
|
G | C | 1 | a0023c0045t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1663-778G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289493 | ||||||
| chr1:1289494
|
T | A | 2 | a0001c0012t0001g0127a0013c0042t0001g0129 | 2 | HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1663-777T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289494 | ||||||
| chr1:1289494
|
T | C | 1 | a0023c0045t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1663-777T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289494 | ||||||
| chr1:1289494
|
T | TGTCTCTG others(47): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-769_1663-768i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289494 | |||||
| chr1:1289494
|
T | TGTCTCTG others(31): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-761_1663-760i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289494 | |||||
| chr1:1289494
|
TGTCTCTG others(175): Show |
T | 1 | a0001c0001t0001g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1663-760_1663-579d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289494 | |||||
| chr1:1289497
|
C | G | 1 | a0023c0045t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1663-774C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289497 | ||||||
| chr1:1289498
|
T | C | 9 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0011g0267others(6): Show | 9 | HG01175.hp2 HG01433.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663-773T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289498 | ||||||
| chr1:1289498
|
TCTGCTCC others(29): Show |
T | 1 | a0002c0028t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1663-760_1663-725d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289498 | |||||
| chr1:1289498
|
TCTGCTCC others(47): Show |
T | 1 | a0006c0010t0007g0273 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1663-760_1663-707d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289498 | |||||
| chr1:1289498
|
TCTGCTCC others(65): Show |
T | 3 | a0002c0003t0005g0002a0004c0008t0001g0239a0005c0011t0001g0157 | 3 | HG02258.hp1 HG02622.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1663-760_1663-689d others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289498 | |||||
| chr1:1289503
|
T | C | 43 | a0001c0001t0001g0167a0001c0001t0001g0208a0001c0001t0001g0219others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1663-768T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289503 | ||||||
| chr1:1289503
|
T | TCCGTCCC others(65): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-761_1663-760i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289503 | |||||
| chr1:1289506
|
G | A | 4 | a0002c0002t0001g0036a0002c0002t0001g0042a0002c0002t0001g0077others(1): Show | 4 | HG00408.hp2 NA18954.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-765G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289506 | ||||||
| chr1:1289508
|
C | T | 4 | a0002c0002t0001g0036a0002c0002t0001g0042a0002c0002t0001g0077others(1): Show | 4 | HG00408.hp2 NA18954.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-763C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289508 | ||||||
| chr1:1289509
|
C | CCGTGTCT others(9): Show |
1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1663-761_1663-760i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
C | CCGTGTCT others(227): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1663-761_1663-760i others(236): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
C | CCGTGTCT others(807): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1663-761_1663-760i others(816): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
C | CCGTGTCT others(9): Show |
2 | a0002c0003t0001g0069a0013c0043t0001g0147 | 2 | HG02040.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1663-761_1663-760i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
C | CCGTGTCT others(121): Show |
1 | a0002c0002t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1663-761_1663-760i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
C | CCGTGTCT others(121): Show |
1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1663-761_1663-760i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
CCCCGTGT others(63): Show |
C | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1663-752_1663-683d others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289509
|
CCCCGTGT others(81): Show |
C | 1 | a0003c0004t0003g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1663-752_1663-665d others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289509 | |||||
| chr1:1289511
|
C | A | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1663-760C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289511 | ||||||
| chr1:1289511
|
C | G | 92 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0001g0178others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1663-760C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289511 | ||||||
| chr1:1289512
|
C | CGA | 4 | a0002c0003t0001g0091a0006c0010t0007g0274a0014c0021t0008g0271others(1): Show | 4 | HG01496.hp1 NA18906.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-758_1663-757i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289512 | |||||
| chr1:1289512
|
C | T | 93 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0001g0178others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1663-759C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289512 | ||||||
| chr1:1289515
|
G | C | 97 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0001g0178others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1663-756G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289515 | ||||||
| chr1:1289515
|
G | GTC | 74 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0179others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1663-754_1663-753d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCCCTGC others(13): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1663-754_1663-753i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(49): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1663-753_1663-752i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(15): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1663-753_1663-752i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(1879): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1663-753_1663-752i others(1888): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(149): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1663-753_1663-752i others(158): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(69): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-753_1663-752i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(13): Show |
2 | a0001c0001t0001g0198a0001c0001t0005g0234 | 2 | HG01433.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1663-753_1663-752i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(505): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-753_1663-752i others(514): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289515
|
G | GTCTCTGC others(181): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1663-753_1663-752i others(190): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289515 | |||||
| chr1:1289516
|
T | C | 9 | a0001c0001t0001g0178a0001c0001t0001g0194a0001c0001t0001g0200others(6): Show | 9 | HG01081.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1663-755T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289516 | ||||||
| chr1:1289516
|
T | TCC | 9 | a0001c0001t0001g0162a0001c0001t0001g0202a0001c0001t0001g0212others(6): Show | 9 | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1663-754_1663-753i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289516 | |||||
| chr1:1289516
|
T | TCCCTGCT others(31): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1663-754_1663-753i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289516 | |||||
| chr1:1289516
|
T | TCTCTGCC others(1733): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1663-753_1663-752i others(1742): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289516 | |||||
| chr1:1289516
|
T | TCTCTGCT others(89): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663-753_1663-752i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289516 | |||||
| chr1:1289518
|
TGCTCCGT others(27): Show |
T | 2 | a0001c0001t0001g0201a0001c0001t0002g0221 | 2 | HG01069.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1663-752_1663-719d others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289518 | ||||||
| chr1:1289518
|
TGCTCCGT others(45): Show |
T | 4 | a0002c0002t0001g0085a0003c0004t0003g0137a0003c0004t0003g0148others(1): Show | 4 | HG02896.hp2 HG03195.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-752_1663-701d others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289518 | ||||||
| chr1:1289521
|
T | C | 40 | a0001c0001t0001g0193a0001c0001t0001g0202a0001c0001t0002g0255others(37): Show | 40 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1663-750T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289521 | ||||||
| chr1:1289523
|
C | T | 1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1663-748C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289523 | ||||||
| chr1:1289524
|
G | A | 1 | a0002c0002t0001g0016 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1663-747G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289524 | ||||||
| chr1:1289525
|
T | TCC | 25 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0212others(22): Show | 25 | HG00423.hp1 HG00642.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1663-744_1663-743d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289525 | |||||
| chr1:1289525
|
T | TCCCGTGT others(13): Show |
1 | a0006c0010t0007g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1663-738_1663-737i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289525 | |||||
| chr1:1289527
|
CCGTGTCC others(27): Show |
C | 1 | a0001c0001t0001g0196 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1663-742_1663-709d others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289527 | |||||
| chr1:1289527
|
CCGTGTCC others(45): Show |
C | 1 | a0006c0010t0007g0270 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1663-742_1663-691d others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289527 | |||||
| chr1:1289529
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0187 | 2 | HG02486.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1663-742G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289529 | ||||||
| chr1:1289529
|
G | C | 1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-742G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289529 | ||||||
| chr1:1289530
|
T | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0212a0001c0001t0001g0242 | 3 | HG00642.hp2 HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1663-741T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289530 | ||||||
| chr1:1289530
|
T | C | 1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-741T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289530 | ||||||
| chr1:1289532
|
TCC | T | 3 | a0001c0001t0002g0169a0014c0021t0008g0271a0025c0044t0003g0257 | 3 | HG00408.hp1 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1663-737_1663-736d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289532 | |||||
| chr1:1289533
|
C | CTCTGCCC others(183): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-738_1663-737i others(192): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289533 | ||||||
| chr1:1289533
|
C | CTCTGCTC others(11): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1663-738_1663-737i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289533 | ||||||
| chr1:1289533
|
C | CTCTGCTC others(139): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-738_1663-737i others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289533 | ||||||
| chr1:1289533
|
C | G | 1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-738C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289533 | ||||||
| chr1:1289534
|
C | CCTGCCCC others(47): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-733_1663-732i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289534 | |||||
| chr1:1289534
|
C | CCTGCTCC others(167): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1663-725_1663-724i others(176): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289534 | |||||
| chr1:1289534
|
C | CCTGCTCC others(49): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-725_1663-724i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289534 | |||||
| chr1:1289534
|
C | T | 167 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0175others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1663-737C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289534 | ||||||
| chr1:1289539
|
T | C | 60 | a0001c0001t0001g0165a0001c0001t0001g0179a0001c0001t0001g0200others(57): Show | 60 | HG00280.hp1 HG00558.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1663-732T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289539 | ||||||
| chr1:1289539
|
T | TCCGTCCC others(49): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1663-720_1663-719i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289539 | |||||
| chr1:1289539
|
T | TCCGTCCC others(137): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1663-720_1663-719i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289539 | |||||
| chr1:1289542
|
G | A | 5 | a0002c0002t0001g0025a0002c0002t0001g0029a0002c0002t0001g0066others(2): Show | 5 | HG00423.hp1 HG00423.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-729G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289542 | ||||||
| chr1:1289543
|
T | TCC | 47 | a0001c0001t0001g0177a0001c0001t0001g0181a0001c0001t0001g0191others(44): Show | 47 | HG00099.hp1 HG00558.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1663-726_1663-725d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TCCCCCGT others(67): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-725_1663-724i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TCCCCCGT others(15): Show |
1 | a0003c0004t0003g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1663-725_1663-724i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TCCCGTGT others(13): Show |
2 | a0002c0003t0002g0101a0026c0041t0001g0261 | 2 | NA18747.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1663-720_1663-719i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TCCCGTGT others(145): Show |
1 | a0002c0003t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1663-720_1663-719i others(154): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TCCCGTGT others(89): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-720_1663-719i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TCCCGTGT others(147): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1663-720_1663-719i others(156): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289543 | |||||
| chr1:1289543
|
T | TTC | 5 | a0002c0002t0001g0025a0002c0002t0001g0029a0002c0002t0001g0066others(2): Show | 5 | HG00423.hp1 HG00423.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-728_1663-727i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289543 | ||||||
| chr1:1289545
|
CCGTGTCC others(9): Show |
C | 1 | a0003c0004t0003g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1663-724_1663-709d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289545 | |||||
| chr1:1289547
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1663-724G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289547 | ||||||
| chr1:1289548
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1663-723T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289548 | ||||||
| chr1:1289548
|
T | TGTCTCTG others(13): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1663-720_1663-719i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289548 | |||||
| chr1:1289551
|
C | CTCTGCTC others(11): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-720_1663-719i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289551 | ||||||
| chr1:1289551
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1663-720C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289551 | ||||||
| chr1:1289552
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0175others(171): Show | 175 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1663-719C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289552 | ||||||
| chr1:1289552
|
CCTGCTCC others(65): Show |
C | 2 | a0001c0001t0001g0185a0001c0001t0001g0188 | 2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1663-701_1663-630d others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289552 | |||||
| chr1:1289557
|
T | C | 49 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0181others(46): Show | 49 | HG00280.hp1 HG00621.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1663-714T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289557 | ||||||
| chr1:1289557
|
T | TCCGTCCC others(51): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1663-707_1663-706i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289557 | |||||
| chr1:1289560
|
G | A | 2 | a0007c0006t0001g0070a0009c0013t0001g0040 | 2 | HG00438.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1663-711G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289560 | ||||||
| chr1:1289560
|
G | C | 1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-711G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289560 | ||||||
| chr1:1289561
|
T | TCC | 32 | a0001c0001t0001g0200a0001c0001t0001g0208a0001c0001t0001g0217others(29): Show | 32 | HG00280.hp2 HG00621.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1663-708_1663-707d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289561
|
T | TCCCCCGT others(35): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-707_1663-706i others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289561
|
T | TCCCCCGT others(54): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1663-707_1663-706i others(63): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289561
|
T | TCCCCCGT others(53): Show |
1 | a0020c0030t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1663-707_1663-706i others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289561
|
T | TCCCGTGT others(13): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1663-702_1663-701i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289561
|
T | TCCCGTGT others(87): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1663-702_1663-701i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289561
|
T | TCCCGTGT others(51): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1663-702_1663-701i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289561 | |||||
| chr1:1289563
|
CCGTGTCC others(9): Show |
C | 4 | a0001c0012t0001g0131a0002c0002t0001g0058a0002c0003t0004g0118others(1): Show | 4 | HG01517.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-706_1663-691d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289563 | |||||
| chr1:1289565
|
G | C | 2 | a0002c0002t0001g0109a0004c0008t0001g0240 | 2 | HG02976.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1663-706G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289565 | ||||||
| chr1:1289566
|
T | A | 2 | a0001c0001t0001g0208a0001c0018t0005g0224 | 2 | HG00280.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1663-705T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289566 | ||||||
| chr1:1289566
|
T | C | 2 | a0002c0002t0001g0109a0004c0008t0001g0240 | 2 | HG02976.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1663-705T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289566 | ||||||
| chr1:1289566
|
T | TGTCTCTG others(31): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1663-702_1663-701i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289566 | |||||
| chr1:1289569
|
C | CTGCTCCG others(47): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1663-702_1663-701i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289569 | ||||||
| chr1:1289569
|
C | G | 2 | a0002c0002t0001g0109a0004c0008t0001g0240 | 2 | HG02976.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1663-702C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289569 | ||||||
| chr1:1289570
|
C | CCTGCTCC others(67): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-689_1663-688i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289570 | |||||
| chr1:1289570
|
C | CCTGCTCC others(325): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1663-679_1663-678i others(334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289570 | |||||
| chr1:1289570
|
C | CCTGCTCC others(31): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1663-671_1663-670i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289570 | |||||
| chr1:1289570
|
C | T | 184 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0165others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1663-701C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289570 | ||||||
| chr1:1289575
|
T | C | 55 | a0001c0001t0001g0162a0001c0001t0001g0195a0001c0001t0001g0197others(52): Show | 55 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1663-696T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289575 | ||||||
| chr1:1289575
|
T | TCCGTCCC others(51): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1663-689_1663-688i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289575 | |||||
| chr1:1289575
|
T | TCCGTCCC others(395): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-689_1663-688i others(404): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289575 | |||||
| chr1:1289577
|
C | T | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663-694C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289577 | ||||||
| chr1:1289578
|
G | A | 4 | a0002c0002t0001g0034a0002c0002t0001g0047a0002c0002t0001g0077others(1): Show | 4 | HG01081.hp2 HG01952.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-693G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289578 | ||||||
| chr1:1289579
|
T | TCC | 38 | a0001c0001t0001g0175a0001c0001t0001g0186a0001c0001t0001g0194others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1663-690_1663-689d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCCCGT others(185): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1663-689_1663-688i others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCCCGT others(187): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1663-689_1663-688i others(196): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCGTGT others(165): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1663-684_1663-683i others(174): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCGTGT others(93): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1663-679_1663-678i others(102): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCGTGT others(271): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1663-679_1663-678i others(280): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCGTGT others(445): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663-671_1663-670i others(454): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TCCCGTGT others(209): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-683_1663-682i others(218): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289579 | |||||
| chr1:1289579
|
T | TTC | 3 | a0002c0002t0001g0047a0002c0002t0001g0077a0009c0013t0001g0078 | 3 | HG01952.hp1 NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1663-692_1663-691i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289579 | ||||||
| chr1:1289583
|
G | C | 4 | a0001c0001t0001g0207a0001c0001t0002g0260a0002c0002t0001g0045others(1): Show | 4 | HG02523.hp1 HG02523.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-688G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289583 | ||||||
| chr1:1289584
|
T | A | 7 | a0001c0001t0001g0194a0001c0012t0001g0127a0001c0012t0001g0131others(4): Show | 7 | HG01261.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-687T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289584 | ||||||
| chr1:1289584
|
T | C | 4 | a0001c0001t0001g0207a0001c0001t0002g0260a0002c0002t0001g0045others(1): Show | 4 | HG02523.hp1 HG02523.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-687T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289584 | ||||||
| chr1:1289584
|
T | TGTCTCTG others(65): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-679_1663-678i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289584 | |||||
| chr1:1289587
|
C | G | 4 | a0001c0001t0001g0207a0001c0001t0002g0260a0002c0002t0001g0045others(1): Show | 4 | HG02523.hp1 HG02523.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-684C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289587 | ||||||
| chr1:1289588
|
T | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0198others(11): Show | 14 | HG00099.hp2 HG01256.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1663-683T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289588 | ||||||
| chr1:1289593
|
T | C | 45 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0200others(42): Show | 45 | HG00558.hp1 HG00621.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1663-678T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289593 | ||||||
| chr1:1289593
|
T | TCCGTCCC others(103): Show |
1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-671_1663-670i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289593 | |||||
| chr1:1289593
|
T | TCCGTCCC others(67): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-658_1663-657i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289593 | |||||
| chr1:1289596
|
G | A | 2 | a0002c0002t0001g0053a0002c0002t0001g0085 | 2 | NA18747.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1663-675G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289596 | ||||||
| chr1:1289597
|
T | TCC | 34 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0193others(31): Show | 34 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1663-672_1663-671d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289597
|
T | TCCCCCGA others(51): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1663-671_1663-670i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289597
|
T | TCCCCCGT others(55): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-671_1663-670i others(64): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289597
|
T | TCCCCCGT others(149): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1663-671_1663-670i others(158): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289597
|
T | TCCCCCGT others(53): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-671_1663-670i others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289597
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-671_1663-670i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289597
|
T | TCCCGTGT others(123): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1663-635_1663-634i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289597 | |||||
| chr1:1289599
|
CCGTGTCT others(27): Show |
C | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1663-670_1663-637d others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289599 | |||||
| chr1:1289601
|
G | C | 2 | a0001c0001t0001g0242a0030c0024t0001g0051 | 2 | HG02922.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1663-670G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289601 | ||||||
| chr1:1289602
|
T | A | 3 | a0001c0009t0001g0218a0001c0047t0001g0183a0004c0008t0001g0262 | 3 | HG00099.hp2 HG02300.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1663-669T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289602 | ||||||
| chr1:1289602
|
T | C | 2 | a0001c0001t0001g0242a0030c0024t0001g0051 | 2 | HG02922.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1663-669T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289602 | ||||||
| chr1:1289605
|
C | G | 2 | a0001c0001t0001g0242a0030c0024t0001g0051 | 2 | HG02922.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1663-666C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289605 | ||||||
| chr1:1289606
|
T | C | 16 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0186others(13): Show | 16 | HG00639.hp2 HG00741.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-665T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289606 | ||||||
| chr1:1289606
|
T | TCTGCCCC others(197): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-661_1663-660i others(206): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289606 | |||||
| chr1:1289606
|
T | TCTGCTCC others(878): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1663-653_1663-652i others(887): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289606 | |||||
| chr1:1289607
|
C | G | 1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1663-664C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289607 | ||||||
| chr1:1289611
|
T | C | 51 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0197others(48): Show | 51 | HG00280.hp2 HG00621.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1663-660T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289611 | ||||||
| chr1:1289611
|
T | TCCGTCCC others(147): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1663-653_1663-652i others(156): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289611 | |||||
| chr1:1289611
|
T | TCCGTCCC others(425): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-643_1663-642i others(434): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289611 | |||||
| chr1:1289614
|
G | A | 5 | a0002c0002t0001g0035a0002c0002t0001g0076a0002c0003t0001g0026others(2): Show | 5 | HG01243.hp1 HG02145.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-657G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289614 | ||||||
| chr1:1289615
|
T | TCC | 34 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0168others(31): Show | 34 | HG00597.hp1 HG00741.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1663-654_1663-653d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(831): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1663-653_1663-652i others(840): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(399): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1663-653_1663-652i others(408): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(33): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1663-653_1663-652i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(219): Show |
1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1663-653_1663-652i others(228): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(35): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1663-653_1663-652i others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(147): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1663-653_1663-652i others(156): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1663-653_1663-652i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCGTGT others(13): Show |
1 | a0027c0039t0002g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1663-643_1663-642i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCGTGT others(215): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1663-643_1663-642i others(224): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TCCCGTGT others(13): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1663-640_1663-639i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289615
|
T | TTC | 5 | a0002c0002t0001g0035a0002c0002t0001g0076a0002c0003t0001g0026others(2): Show | 5 | HG01243.hp1 HG02145.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-656_1663-655i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289615 | ||||||
| chr1:1289615
|
TCCCGTGT others(105): Show |
T | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1663-634_1663-523d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289615 | |||||
| chr1:1289617
|
CCGTGTCT others(9): Show |
C | 1 | a0003c0004t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1663-652_1663-637d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289617 | |||||
| chr1:1289617
|
CCGTGTCT others(179): Show |
C | 4 | a0003c0004t0003g0133a0003c0004t0003g0135a0003c0004t0003g0153others(1): Show | 4 | NA18964.hp2 NA18998.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-652_1663-467d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289617 | |||||
| chr1:1289617
|
CCGTGTCT others(412): Show |
C | 1 | a0024c0033t0009g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1663-652_1663-234d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289617 | |||||
| chr1:1289619
|
G | C | 3 | a0001c0001t0001g0177a0004c0008t0001g0239a0004c0008t0001g0241 | 3 | HG01109.hp1 HG02258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1663-652G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289619 | ||||||
| chr1:1289620
|
T | A | 2 | a0001c0001t0001g0166a0001c0001t0005g0234 | 2 | HG00741.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1663-651T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289620 | ||||||
| chr1:1289620
|
T | C | 3 | a0001c0001t0001g0177a0004c0008t0001g0239a0004c0008t0001g0241 | 3 | HG01109.hp1 HG02258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1663-651T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289620 | ||||||
| chr1:1289620
|
TGTCTCTG others(232): Show |
T | 1 | a0003c0004t0003g0005 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1663-611_1663-373d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289620 | |||||
| chr1:1289623
|
C | G | 3 | a0001c0001t0001g0177a0004c0008t0001g0239a0004c0008t0001g0241 | 3 | HG01109.hp1 HG02258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1663-648C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289623 | ||||||
| chr1:1289624
|
T | C | 15 | a0001c0001t0001g0162a0001c0001t0001g0180a0001c0001t0001g0186others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663-647T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289624 | ||||||
| chr1:1289629
|
T | C | 51 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0192others(48): Show | 51 | HG00558.hp1 HG00621.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1663-642T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289629 | ||||||
| chr1:1289629
|
T | TCCGTCCC others(71): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1663-635_1663-634i others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289629 | |||||
| chr1:1289629
|
T | TCCGTCCC others(771): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1663-612_1663-611i others(780): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289629 | |||||
| chr1:1289632
|
G | A | 1 | a0002c0002t0001g0059 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1663-639G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289632 | ||||||
| chr1:1289633
|
T | TCC | 29 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0181others(26): Show | 29 | HG00544.hp1 HG00741.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1663-636_1663-635d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCCCGT others(109): Show |
1 | a0001c0001t0002g0140 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1663-635_1663-634i others(118): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCCCGT others(245): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-635_1663-634i others(254): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCCCGT others(165): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1663-635_1663-634i others(174): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCCCGT others(87): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1663-635_1663-634i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCCCGT others(13): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-635_1663-634i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCGTGT others(1220): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-625_1663-624i others(1229): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289633
|
T | TCCCGTGT others(33): Show |
1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1663-617_1663-616i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289633 | |||||
| chr1:1289635
|
CCGTGTCT others(47): Show |
C | 1 | a0006c0010t0007g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1663-634_1663-581d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289635 | |||||
| chr1:1289635
|
CCGTGTCT others(230): Show |
C | 1 | a0021c0032t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1663-634_1663-398d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289635 | |||||
| chr1:1289638
|
TGTCTCTG others(31): Show |
T | 1 | a0004c0008t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1663-611_1663-574d others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289638 | |||||
| chr1:1289638
|
TGTCTCTG others(214): Show |
T | 1 | a0001c0001t0011g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1663-611_1663-391d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289638 | |||||
| chr1:1289641
|
C | CTCTGCTC others(51): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-617_1663-616i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289641 | |||||
| chr1:1289641
|
CTCTGCTC others(324): Show |
C | 1 | a0002c0002t0001g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1663-598_1663-268d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289641 | |||||
| chr1:1289642
|
T | C | 18 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0177others(15): Show | 18 | HG00099.hp1 HG00544.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-629T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289642 | ||||||
| chr1:1289642
|
TCTGCTCC others(11): Show |
T | 2 | a0001c0001t0001g0209a0001c0001t0002g0221 | 2 | HG01192.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1663-616_1663-599d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289642 | |||||
| chr1:1289644
|
T | TGCTCCGT others(105): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663-612_1663-611i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289644 | |||||
| chr1:1289647
|
T | C | 45 | a0001c0001t0001g0167a0001c0001t0001g0192a0001c0001t0001g0193others(42): Show | 45 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1663-624T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289647 | ||||||
| chr1:1289647
|
T | TCCGTCCC others(31): Show |
1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1663-617_1663-616i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289647 | |||||
| chr1:1289647
|
T | TCCGTCCC others(1537): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663-612_1663-611i others(1546): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289647 | |||||
| chr1:1289650
|
G | A | 2 | a0002c0002t0001g0016a0003c0004t0003g0142 | 2 | HG00558.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1663-621G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289650 | ||||||
| chr1:1289651
|
T | TCC | 24 | a0001c0001t0001g0194a0001c0001t0001g0212a0001c0001t0001g0237others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.1663-618_1663-617d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289651 | |||||
| chr1:1289651
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1663-617_1663-616i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289651 | |||||
| chr1:1289651
|
T | TCCCCCGT others(31): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-617_1663-616i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289651 | |||||
| chr1:1289651
|
T | TCCCGTGT others(67): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-612_1663-611i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289651 | |||||
| chr1:1289651
|
T | TCCGTGTC others(185): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1663-618_1663-617i others(194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289651 | |||||
| chr1:1289653
|
CCGTGTCC others(29): Show |
C | 3 | a0002c0002t0001g0025a0006c0010t0007g0270a0008c0007t0004g0287 | 3 | HG00738.hp1 HG03195.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1663-616_1663-581d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289653 | |||||
| chr1:1289653
|
CCGTGTCC others(212): Show |
C | 1 | a0002c0002t0001g0079 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1663-616_1663-398d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289653 | |||||
| chr1:1289655
|
G | C | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1663-616G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289655 | ||||||
| chr1:1289656
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1663-615T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289656 | ||||||
| chr1:1289656
|
TGTCCCTG others(13): Show |
T | 3 | a0002c0002t0001g0035a0002c0003t0005g0002a0005c0011t0001g0157 | 3 | HG02622.hp2 NA19004.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1663-611_1663-592d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289656 | |||||
| chr1:1289659
|
C | G | 2 | a0002c0002t0001g0080a0025c0044t0003g0257 | 2 | HG02523.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1663-612C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289659 | ||||||
| chr1:1289660
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1663-611C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289660 | ||||||
| chr1:1289660
|
CCTGCTCC others(214): Show |
C | 3 | a0003c0004t0003g0146a0003c0004t0003g0151a0003c0004t0003g0154 | 3 | NA18998.hp1 NA19057.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1663-598_1663-378d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289660 | |||||
| chr1:1289665
|
T | C | 53 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0167others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1663-606T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289665 | ||||||
| chr1:1289665
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-599_1663-598i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289665 | |||||
| chr1:1289667
|
C | T | 1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1663-604C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289667 | ||||||
| chr1:1289668
|
G | A | 11 | a0002c0002t0001g0011a0002c0002t0001g0013a0002c0002t0001g0017others(8): Show | 11 | HG00438.hp1 HG01943.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.1663-603G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289668 | ||||||
| chr1:1289669
|
TCC | T | 69 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0168others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1663-598_1663-597d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289669 | |||||
| chr1:1289670
|
C | T | 10 | a0002c0002t0001g0011a0002c0002t0001g0013a0002c0002t0001g0017others(7): Show | 10 | HG00438.hp1 HG01943.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1663-601C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289670 | ||||||
| chr1:1289671
|
C | CCCCGTGT others(49): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1663-596_1663-595i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCC others(9): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1663-599_1663-598i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCC others(81): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1663-599_1663-598i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(9): Show |
2 | a0001c0001t0001g0166a0002c0002t0001g0034 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1663-599_1663-598i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(29): Show |
1 | a0003c0004t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1663-599_1663-598i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(45): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0197 | 2 | HG02109.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1663-599_1663-598i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(45): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1663-599_1663-598i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(121): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1663-599_1663-598i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(9): Show |
7 | a0001c0001t0001g0214a0001c0001t0002g0161a0002c0002t0001g0029others(4): Show | 7 | HG00423.hp1 HG01517.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-599_1663-598i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(49): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1663-599_1663-598i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(29): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1663-599_1663-598i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(123): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-599_1663-598i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
C | CCGTGTCT others(291): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-599_1663-598i others(300): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289671
|
CCCCGAGT others(11): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1663-595_1663-578d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289671 | |||||
| chr1:1289672
|
C | CGTGTCTC others(8): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1663-599_1663-598i others(17): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289672 | ||||||
| chr1:1289674
|
CGA | C | 3 | a0003c0004t0003g0152a0004c0008t0001g0262a0016c0031t0001g0092 | 3 | HG03579.hp2 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1663-595_1663-594d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289674 | |||||
| chr1:1289675
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0003t0001g0060 | 3 | HG01081.hp1 HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1663-596G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289675 | ||||||
| chr1:1289676
|
A | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1663-595A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289676 | ||||||
| chr1:1289679
|
C | CTCTGCTC others(321): Show |
1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1663-566_1663-565i others(330): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289679 | |||||
| chr1:1289679
|
C | CTGCTCCG others(7): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-591_1663-590i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289679 | |||||
| chr1:1289679
|
C | CTGCTCCG others(925): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-591_1663-590i others(934): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289679 | |||||
| chr1:1289679
|
C | CTGCTCCG others(99): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-591_1663-590i others(108): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289679 | |||||
| chr1:1289679
|
C | G | 3 | a0004c0005t0010g0124a0004c0008t0001g0262a0016c0031t0001g0092 | 3 | HG03209.hp2 HG03579.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1663-592C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289679 | ||||||
| chr1:1289680
|
T | C | 15 | a0001c0001t0001g0167a0001c0001t0001g0193a0001c0001t0001g0194others(12): Show | 15 | HG00438.hp1 HG00639.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663-591T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289680 | ||||||
| chr1:1289685
|
T | C | 43 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0178others(40): Show | 43 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1663-586T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289685 | ||||||
| chr1:1289685
|
T | TCCGTCCC others(49): Show |
1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1663-575_1663-574i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289685 | |||||
| chr1:1289685
|
T | TCTGTCCC others(143): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1663-585_1663-584i others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289685 | |||||
| chr1:1289689
|
T | TCC | 27 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0213others(24): Show | 27 | HG00544.hp2 HG00741.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1663-580_1663-579d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCCCGT others(145): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1663-579_1663-578i others(154): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCCCGT others(73): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-579_1663-578i others(82): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCCCGT others(165): Show |
1 | a0002c0003t0004g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1663-579_1663-578i others(174): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCCCGT others(91): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1663-579_1663-578i others(100): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCGTGT others(1185): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1663-569_1663-568i others(1194): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCGTGT others(505): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1663-569_1663-568i others(514): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289689
|
T | TCCCGTGT others(257): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1663-569_1663-568i others(266): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289689 | |||||
| chr1:1289691
|
CCGTGTCT others(9): Show |
C | 1 | a0002c0002t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1663-578_1663-563d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289691 | |||||
| chr1:1289691
|
CCGTGTCT others(174): Show |
C | 4 | a0002c0002t0001g0057a0002c0002t0001g0062a0002c0002t0001g0076others(1): Show | 4 | HG00673.hp1 HG02074.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-578_1663-398d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289691 | |||||
| chr1:1289691
|
CCGTGTCT others(284): Show |
C | 1 | a0014c0021t0008g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1663-578_1663-288d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289691 | |||||
| chr1:1289693
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-578G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289693 | ||||||
| chr1:1289694
|
T | A | 1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-577T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289694 | ||||||
| chr1:1289694
|
TGTCTCTG others(158): Show |
T | 2 | a0003c0004t0003g0144a0009c0013t0001g0078 | 2 | NA18970.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1663-555_1663-391d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289694 | |||||
| chr1:1289696
|
TCTCTGCT others(288): Show |
T | 1 | a0001c0001t0001g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1663-572_1663-278d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289696 | |||||
| chr1:1289698
|
T | C | 19 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0187others(16): Show | 19 | HG00639.hp1 HG00673.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1663-573T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289698 | ||||||
| chr1:1289698
|
TCTGCTCC others(304): Show |
T | 2 | a0001c0020t0001g0176a0002c0002t0001g0047 | 2 | HG01169.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1663-555_1663-245d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289698 | |||||
| chr1:1289703
|
T | C | 46 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0175others(43): Show | 46 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1663-568T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289703 | ||||||
| chr1:1289703
|
T | TCCGTCCC others(49): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-561_1663-560i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289703 | |||||
| chr1:1289706
|
G | A | 1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-565G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289706 | ||||||
| chr1:1289707
|
T | TCC | 25 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0212others(22): Show | 25 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1663-562_1663-561d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
T | TCCCCCGT others(33): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1663-561_1663-560i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
T | TCCCCCGT others(125): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1663-561_1663-560i others(134): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
T | TCCCCGTG others(2679): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1663-561_1663-560i others(2688): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
T | TCCCGTGT others(49): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1663-556_1663-555i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
T | TCCCGTGT others(31): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663-556_1663-555i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
TCCCGTGT others(13): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1663-555_1663-536d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289707
|
TCCCGTGT others(32): Show |
T | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1663-560_1663-522d others(41): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289707 | |||||
| chr1:1289709
|
CCGTGTCC others(49): Show |
C | 1 | a0002c0002t0001g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1663-560_1663-505d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289709 | |||||
| chr1:1289709
|
CCGTGTCC others(466): Show |
C | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1663-560_1663-88de others(1): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289709 | |||||
| chr1:1289711
|
G | C | 2 | a0001c0001t0002g0260a0001c0047t0001g0183 | 2 | HG00099.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1663-560G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289711 | ||||||
| chr1:1289712
|
T | C | 2 | a0001c0001t0002g0260a0001c0047t0001g0183 | 2 | HG00099.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1663-559T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289712 | ||||||
| chr1:1289715
|
C | CTGCTCCG others(7): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-556_1663-555i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289715 | ||||||
| chr1:1289715
|
C | G | 2 | a0001c0001t0002g0260a0001c0047t0001g0183 | 2 | HG00099.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1663-556C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289715 | ||||||
| chr1:1289715
|
CCCTGCTC others(250): Show |
C | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1663-555_1663-299d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289715 | ||||||
| chr1:1289716
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1663-555C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289716 | ||||||
| chr1:1289716
|
CCTGCTCC others(158): Show |
C | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663-542_1663-378d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289716 | |||||
| chr1:1289721
|
T | C | 45 | a0001c0001t0001g0178a0001c0001t0001g0194a0001c0001t0001g0200others(42): Show | 45 | HG00597.hp1 HG00673.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1663-550T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289721 | ||||||
| chr1:1289721
|
T | TCCGTCCC others(49): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289721 | |||||
| chr1:1289721
|
T | TCCGTCCC others(65): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289721 | |||||
| chr1:1289724
|
G | A | 10 | a0002c0002t0001g0016a0002c0002t0001g0023a0002c0002t0001g0033others(7): Show | 10 | HG02004.hp1 HG02258.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-547G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289724 | ||||||
| chr1:1289725
|
TCC | T | 85 | a0001c0001t0001g0165a0001c0001t0001g0177a0001c0001t0001g0178others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1663-542_1663-541d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289725 | |||||
| chr1:1289725
|
TCCCCCGT others(15): Show |
T | 1 | a0003c0004t0003g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1663-542_1663-521d others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289725 | |||||
| chr1:1289726
|
C | CCCCCGTG others(70): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1663-531_1663-530i others(79): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289726 | |||||
| chr1:1289726
|
C | CCCGTGTC others(89): Show |
1 | a0020c0030t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(98): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289726 | |||||
| chr1:1289726
|
C | T | 9 | a0002c0002t0001g0016a0002c0002t0001g0033a0002c0002t0001g0042others(6): Show | 9 | HG02258.hp1 HG02300.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663-545C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289726 | ||||||
| chr1:1289727
|
C | CCCCGTGT others(85): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1663-531_1663-530i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCCCGTGT others(9): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-535_1663-534i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCC others(27): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCC others(29): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCC others(83): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1663-543_1663-542i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCC others(81): Show |
1 | a0006c0010t0007g0275 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(9): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(47): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(157): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(166): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(211): Show |
1 | a0002c0003t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(220): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(63): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(9): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(81): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(45): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(45): Show |
1 | a0002c0003t0002g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(357): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(366): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(159): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(4283): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-543_1663-542i others(4292): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(539): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(548): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
C | CCGTGTCT others(337): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-543_1663-542i others(346): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289727
|
CCCCGTGT others(156): Show |
C | 1 | a0002c0002t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1663-522_1663-360d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289727 | |||||
| chr1:1289729
|
C | G | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1663-542C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289729 | ||||||
| chr1:1289730
|
C | T | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1663-541C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289730 | ||||||
| chr1:1289732
|
T | A | 2 | a0001c0001t0005g0234a0005c0011t0001g0157 | 2 | HG02622.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1663-539T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289732 | ||||||
| chr1:1289733
|
G | C | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1663-538G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289733 | ||||||
| chr1:1289733
|
GTC | G | 3 | a0001c0001t0001g0238a0003c0004t0003g0171a0004c0008t0001g0241 | 3 | HG01109.hp1 HG02717.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1663-534_1663-533d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289733 | |||||
| chr1:1289736
|
T | C | 12 | a0001c0001t0001g0197a0001c0001t0001g0208a0001c0001t0001g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1663-535T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289736 | ||||||
| chr1:1289736
|
T | TCTGCCCC others(65): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1663-531_1663-530i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289736 | |||||
| chr1:1289737
|
C | G | 1 | a0002c0002t0001g0085 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1663-534C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289737 | ||||||
| chr1:1289741
|
T | C | 59 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0168others(56): Show | 59 | HG00597.hp1 HG00738.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1663-530T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289741 | ||||||
| chr1:1289741
|
T | TCCGTCCC others(11): Show |
1 | a0001c0001t0002g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289741 | |||||
| chr1:1289744
|
G | A | 11 | a0002c0002t0001g0003a0002c0002t0001g0017a0002c0002t0001g0030others(8): Show | 11 | HG00423.hp2 HG00438.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1663-527G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289744 | ||||||
| chr1:1289745
|
TCC | T | 91 | a0001c0001t0001g0175a0001c0001t0001g0187a0001c0001t0001g0188others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1663-522_1663-521d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289745 | |||||
| chr1:1289745
|
TCCCCCGT others(102): Show |
T | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1663-522_1663-414d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289745 | |||||
| chr1:1289745
|
TCCCCCGT others(120): Show |
T | 1 | a0002c0003t0004g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1663-522_1663-396d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289745 | |||||
| chr1:1289746
|
C | CCCGTGTC others(143): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289746 | |||||
| chr1:1289746
|
C | CCCGTGTC others(67): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289746 | |||||
| chr1:1289746
|
C | T | 10 | a0002c0002t0001g0003a0002c0002t0001g0017a0002c0002t0001g0030others(7): Show | 10 | HG00423.hp2 HG00438.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-525C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289746 | ||||||
| chr1:1289747
|
C | CCCCGTGT others(321): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-511_1663-510i others(330): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCCCGTGT others(11): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1663-502_1663-485d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCCCGTGT others(409): Show |
1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-515_1663-514i others(418): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCC others(63): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCC others(488): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(497): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCC others(249): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(258): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(67): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(388): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(397): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(65): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(65): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(45): Show |
1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(45): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(9): Show |
4 | a0001c0001t0001g0193a0001c0001t0001g0208a0001c0001t0002g0236others(1): Show | 4 | HG00280.hp2 HG02135.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-523_1663-522i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(101): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(163): Show |
1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(172): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(177): Show |
1 | a0002c0002t0001g0023 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(186): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(307): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-523_1663-522i others(316): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289747
|
C | CCGTGTCT others(395): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-523_1663-522i others(404): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289747 | |||||
| chr1:1289752
|
T | A | 4 | a0001c0001t0001g0216a0003c0004t0003g0148a0004c0008t0001g0262others(1): Show | 4 | HG00741.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-519T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289752 | ||||||
| chr1:1289756
|
T | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0191a0001c0001t0001g0204others(3): Show | 6 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-515T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289756 | ||||||
| chr1:1289761
|
T | A | 1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1663-510T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289761 | ||||||
| chr1:1289761
|
T | C | 35 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0192others(32): Show | 35 | HG00280.hp1 HG00558.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1663-510T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289761 | ||||||
| chr1:1289761
|
T | TCCGTCCC others(257): Show |
1 | a0002c0002t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1663-503_1663-502i others(266): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289761 | |||||
| chr1:1289761
|
T | TCCGTCCC others(84): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1663-493_1663-492i others(93): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289761 | |||||
| chr1:1289764
|
G | A | 4 | a0002c0003t0002g0099a0003c0004t0003g0142a0003c0004t0003g0171others(1): Show | 4 | HG00558.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-507G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289764 | ||||||
| chr1:1289765
|
T | TCC | 12 | a0001c0001t0001g0203a0001c0001t0001g0217a0002c0002t0001g0094others(9): Show | 12 | HG00735.hp2 HG01934.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1663-504_1663-503d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289765 | |||||
| chr1:1289765
|
T | TCCCCCGT others(71): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1663-503_1663-502i others(80): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289765 | |||||
| chr1:1289765
|
T | TCCCGTGT others(13): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1663-493_1663-492i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289765 | |||||
| chr1:1289765
|
T | TCCCGTGT others(69): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1663-478_1663-477i others(78): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289765 | |||||
| chr1:1289766
|
C | T | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1663-505C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289766 | ||||||
| chr1:1289767
|
CCGTGTCT others(98): Show |
C | 1 | a0009c0014t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1663-502_1663-398d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289767 | |||||
| chr1:1289767
|
CCGTGTCT others(226): Show |
C | 1 | a0002c0002t0001g0013 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1663-502_1663-270d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289767 | |||||
| chr1:1289768
|
C | T | 1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1663-503C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289768 | ||||||
| chr1:1289769
|
G | C | 1 | a0003c0004t0003g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1663-502G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289769 | ||||||
| chr1:1289770
|
T | A | 2 | a0002c0002t0001g0053a0003c0004t0003g0145 | 2 | HG03490.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1663-501T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289770 | ||||||
| chr1:1289770
|
T | C | 1 | a0003c0004t0003g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1663-501T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289770 | ||||||
| chr1:1289770
|
TGTCTCTG others(82): Show |
T | 3 | a0002c0002t0001g0052a0002c0002t0001g0086a0006c0010t0007g0273 | 3 | HG00544.hp1 HG00597.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1663-484_1663-396d others(91): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289770 | |||||
| chr1:1289773
|
C | G | 1 | a0003c0004t0003g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1663-498C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289773 | ||||||
| chr1:1289773
|
CTCTGCTC others(192): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1663-484_1663-286d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289773 | |||||
| chr1:1289774
|
T | C | 19 | a0001c0001t0001g0167a0001c0001t0001g0189a0001c0001t0001g0190others(16): Show | 19 | HG00099.hp1 HG00438.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1663-497T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289774 | ||||||
| chr1:1289774
|
TCTGCTCC others(13): Show |
T | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1663-484_1663-465d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289774 | |||||
| chr1:1289774
|
TCTGCTCC others(228): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1663-484_1663-250d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289774 | |||||
| chr1:1289779
|
T | C | 36 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0001g0237others(33): Show | 36 | HG00280.hp1 HG00621.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1663-492T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289779 | ||||||
| chr1:1289779
|
T | TCCGTCCC others(67): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289779 | |||||
| chr1:1289782
|
G | A | 6 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0043others(3): Show | 6 | HG01358.hp2 HG02040.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-489G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289782 | ||||||
| chr1:1289783
|
TCC | T | 94 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0177others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1663-484_1663-483d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289783 | |||||
| chr1:1289783
|
TCCCCCGT others(64): Show |
T | 3 | a0002c0002t0001g0031a0002c0002t0001g0085a0023c0045t0001g0164 | 3 | HG00621.hp2 HG03942.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1663-484_1663-414d others(73): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289783 | |||||
| chr1:1289784
|
C | T | 6 | a0002c0002t0001g0019a0002c0002t0001g0025a0002c0002t0001g0043others(3): Show | 6 | HG01358.hp2 HG02040.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-487C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289784 | ||||||
| chr1:1289785
|
C | CCATGTCC others(9): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCCCGTGT others(319): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1663-478_1663-477i others(328): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCCCGTGT others(11): Show |
1 | a0013c0043t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1663-478_1663-477i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCCCGTGT others(9): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0184 | 3 | HG00735.hp1 HG02293.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1663-478_1663-477i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCCCGTGT others(27): Show |
1 | a0001c0001t0011g0267 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1663-478_1663-477i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCC others(9): Show |
2 | a0001c0001t0001g0238a0001c0009t0001g0218 | 2 | HG02300.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1663-485_1663-484i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCC others(27): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCC others(45): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(49): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(323): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(332): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(203): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(212): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(27): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(47): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(9): Show |
6 | a0001c0001t0001g0179a0001c0001t0001g0212a0002c0002t0001g0068others(3): Show | 6 | HG00642.hp2 HG01255.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-485_1663-484i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(103): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(457): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(466): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(211): Show |
1 | a0001c0001t0001g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(220): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(27): Show |
1 | a0002c0003t0001g0097 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(83): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(137): Show |
1 | a0001c0001t0001g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(101): Show |
1 | a0001c0001t0001g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1663-485_1663-484i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(139): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(47): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-485_1663-484i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(81): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(81): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1663-485_1663-484i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
C | CCGTGTCT others(83): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1663-485_1663-484i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289785
|
CCCCGTGT others(80): Show |
C | 2 | a0001c0001t0001g0207a0004c0008t0001g0239 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1663-477_1663-391d others(89): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289785 | |||||
| chr1:1289789
|
G | A | 2 | a0003c0004t0003g0253a0010c0019t0003g0170 | 2 | HG02155.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1663-482G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289789 | ||||||
| chr1:1289790
|
T | A | 3 | a0001c0001t0001g0189a0002c0002t0001g0037a0002c0003t0001g0112 | 3 | HG02004.hp2 HG02559.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1663-481T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289790 | ||||||
| chr1:1289792
|
TCC | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0198others(3): Show | 6 | HG01261.hp2 HG01433.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-477_1663-476d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289792 | |||||
| chr1:1289793
|
C | CTCTGCTC others(345): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1663-478_1663-477i others(354): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289793 | ||||||
| chr1:1289794
|
C | CCTGCTCC others(29): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-447_1663-446i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289794 | |||||
| chr1:1289794
|
C | T | 182 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0177others(179): Show | 182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1663-477C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289794 | ||||||
| chr1:1289798
|
CTCCGTCC others(42): Show |
C | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1663-464_1663-416d others(51): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289798 | |||||
| chr1:1289799
|
T | C | 33 | a0001c0001t0001g0178a0001c0001t0002g0140a0001c0001t0002g0229others(30): Show | 33 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1663-472T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289799 | ||||||
| chr1:1289799
|
T | TCCGTCCC others(2605): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1663-465_1663-464i others(2614): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289799 | |||||
| chr1:1289801
|
C | T | 4 | a0003c0004t0003g0004a0003c0004t0003g0006a0003c0004t0003g0007others(1): Show | 4 | HG00738.hp1 HG01346.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-470C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289801 | ||||||
| chr1:1289802
|
G | A | 1 | a0002c0002t0001g0042 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1663-469G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289802 | ||||||
| chr1:1289803
|
T | TCC | 18 | a0001c0001t0001g0166a0001c0001t0001g0179a0001c0001t0001g0192others(15): Show | 18 | HG00741.hp1 HG01070.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-466_1663-465d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289803 | |||||
| chr1:1289803
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-465_1663-464i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289803 | |||||
| chr1:1289803
|
T | TCCCGTGT others(31): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1663-455_1663-454i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289803 | |||||
| chr1:1289808
|
T | A | 2 | a0002c0003t0001g0060a0010c0019t0003g0098 | 2 | HG02015.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1663-463T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289808 | ||||||
| chr1:1289808
|
TGTCTCTG others(44): Show |
T | 1 | a0008c0007t0004g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1663-446_1663-396d others(53): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289808 | |||||
| chr1:1289811
|
C | CCCTGCTC others(62): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1663-460_1663-459i others(71): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289811 | ||||||
| chr1:1289811
|
C | G | 1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1663-460C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289811 | ||||||
| chr1:1289812
|
T | C | 20 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0185others(17): Show | 20 | HG00099.hp1 HG00438.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1663-459T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289812 | ||||||
| chr1:1289812
|
T | TCTGCTCC others(1283): Show |
1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1663-447_1663-446i others(1292): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289812 | |||||
| chr1:1289817
|
T | C | 46 | a0001c0001t0001g0162a0001c0001t0001g0180a0001c0001t0001g0187others(43): Show | 46 | HG00558.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1663-454T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289817 | ||||||
| chr1:1289817
|
T | TCCGTCCC others(11): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-447_1663-446i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289817 | |||||
| chr1:1289817
|
T | TCCGTCCC others(47): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-447_1663-446i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289817 | |||||
| chr1:1289819
|
C | T | 1 | a0002c0002t0001g0058 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1663-452C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289819 | ||||||
| chr1:1289820
|
G | A | 14 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0023others(11): Show | 14 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-451G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289820 | ||||||
| chr1:1289821
|
TCC | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0162others(73): Show | 77 | HG00099.hp1 HG00423.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.1663-446_1663-445d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289821 | |||||
| chr1:1289821
|
TCCCCCGT others(26): Show |
T | 2 | a0001c0001t0002g0169a0004c0008t0001g0262 | 2 | HG00408.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1663-446_1663-414d others(35): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289821 | |||||
| chr1:1289821
|
TCCCCCGT others(100): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1663-446_1663-340d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289821 | |||||
| chr1:1289822
|
C | T | 13 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0023others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1663-449C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289822 | ||||||
| chr1:1289823
|
C | CCCCGTCT others(65): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-443_1663-442i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCCCGTGT others(45): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-439_1663-438i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(9): Show |
2 | a0001c0001t0005g0258a0008c0007t0004g0284 | 2 | HG02109.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1663-447_1663-446i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(65): Show |
1 | a0001c0001t0002g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1663-447_1663-446i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(27): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1663-447_1663-446i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(1056): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1663-447_1663-446i others(1065): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(83): Show |
1 | a0002c0003t0002g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1663-447_1663-446i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(9): Show |
1 | a0002c0002t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1663-447_1663-446i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
C | CCGTGTCT others(117): Show |
1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1663-447_1663-446i others(126): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
CCCCGTGT others(42): Show |
C | 2 | a0001c0001t0002g0228a0004c0008t0001g0240 | 2 | HG02976.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1663-434_1663-386d others(51): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
CCCCGTGT others(60): Show |
C | 1 | a0002c0002t0001g0065 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1663-434_1663-368d others(69): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289823
|
CCCCGTGT others(78): Show |
C | 1 | a0003c0004t0003g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1663-426_1663-342d others(87): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289823 | |||||
| chr1:1289827
|
G | A | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1663-444G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289827 | ||||||
| chr1:1289828
|
T | A | 10 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0002g0248others(7): Show | 10 | HG02071.hp2 HG02074.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1663-443T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289828 | ||||||
| chr1:1289828
|
TGTCTCTG others(24): Show |
T | 3 | a0002c0002t0001g0035a0002c0002t0001g0059a0002c0003t0005g0002 | 3 | NA18969.hp2 NA19004.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1663-434_1663-404d others(33): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289828 | |||||
| chr1:1289829
|
GTC | G | 3 | a0001c0001t0001g0250a0001c0020t0001g0263a0002c0002t0001g0080 | 3 | HG02523.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1663-438_1663-437d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289829 | |||||
| chr1:1289829
|
GTCTCTGC others(26): Show |
G | 1 | a0001c0001t0001g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1663-438_1663-406d others(35): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289829 | |||||
| chr1:1289832
|
T | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0178a0001c0001t0001g0194others(10): Show | 14 | HG00741.hp2 HG01081.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-439T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289832 | ||||||
| chr1:1289832
|
TCTGCCCC others(152): Show |
T | 1 | a0005c0011t0001g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1663-434_1663-276d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289832 | |||||
| chr1:1289832
|
TCTGCCCC others(206): Show |
T | 1 | a0009c0013t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1663-434_1663-222d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289832 | |||||
| chr1:1289836
|
CCCCGTCC others(4): Show |
C | 7 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0196others(4): Show | 8 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-434_1663-424d others(13): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289836 | ||||||
| chr1:1289837
|
C | T | 123 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0175others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1663-434C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289837 | ||||||
| chr1:1289837
|
CCCGTCCC others(4): Show |
C | 8 | a0001c0001t0002g0140a0002c0002t0001g0037a0003c0004t0003g0133others(5): Show | 8 | HG00738.hp1 HG01496.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-426_1663-416d others(13): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289837 | |||||
| chr1:1289837
|
CCCGTCCC others(42): Show |
C | 1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1663-421_1663-373d others(51): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289837 | |||||
| chr1:1289837
|
CCCGTCCC others(152): Show |
C | 1 | a0002c0028t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1663-420_1663-262d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289837 | |||||
| chr1:1289837
|
CCCGTCCC others(352): Show |
C | 1 | a0004c0005t0006g0128 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1663-421_1663-63de others(1): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289837 | |||||
| chr1:1289840
|
G | A | 2 | a0002c0002t0001g0066a0004c0008t0001g0241 | 2 | HG01109.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1663-431G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289840 | ||||||
| chr1:1289841
|
T | TCC | 14 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0002g0233others(11): Show | 14 | HG01070.hp2 HG01123.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-428_1663-427d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289841 | |||||
| chr1:1289841
|
TCCCGTGT others(80): Show |
T | 1 | a0016c0031t0001g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1663-421_1663-335d others(89): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289841 | |||||
| chr1:1289842
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1663-429C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289842 | ||||||
| chr1:1289843
|
CCGTGTCC others(22): Show |
C | 1 | a0002c0002t0001g0017 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1663-426_1663-398d others(31): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(40): Show |
C | 2 | a0001c0001t0001g0246a0002c0003t0002g0082 | 2 | HG02683.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1663-426_1663-380d others(49): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(58): Show |
C | 1 | a0002c0002t0001g0010 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1663-426_1663-362d others(67): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(132): Show |
C | 1 | a0005c0011t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1663-426_1663-288d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(168): Show |
C | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1663-426_1663-252d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(240): Show |
C | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1663-426_1663-180d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(258): Show |
C | 4 | a0001c0001t0002g0229a0003c0004t0003g0004a0003c0004t0003g0006others(1): Show | 4 | HG01346.hp1 NA18961.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-426_1663-162d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289843
|
CCGTGTCC others(314): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1663-426_1663-106d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289843 | |||||
| chr1:1289845
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663-426G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289845 | ||||||
| chr1:1289846
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663-425T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289846 | ||||||
| chr1:1289846
|
TGTCCGTC others(6): Show |
T | 27 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189others(24): Show | 27 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1663-421_1663-409d others(15): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289846 | |||||
| chr1:1289847
|
G | C | 1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-424G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289847 | ||||||
| chr1:1289847
|
G | GAGTCTCT others(528): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663-424_1663-423i others(537): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289847 | ||||||
| chr1:1289847
|
G | GTCCCTGC | 8 | a0001c0001t0001g0165a0001c0001t0001g0191a0001c0012t0001g0130others(5): Show | 8 | HG00099.hp1 HG01109.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-421_1663-420i others(9): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCCCTGC others(1370): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-421_1663-420i others(1379): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCCCTGC others(36): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1663-421_1663-420i others(45): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCCCTGC others(90): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-421_1663-420i others(99): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC | 27 | a0001c0001t0001g0186a0001c0001t0001g0192a0001c0001t0001g0194others(24): Show | 27 | HG01070.hp1 HG01123.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1663-422_1663-421i others(9): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(1366): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(1375): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(92): Show |
1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(101): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(280): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(289): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(76): Show |
1 | a0002c0003t0004g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(85): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(2258): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(2267): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(72): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(81): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(850): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(859): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(1272): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(1281): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(36): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(45): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(842): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(851): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(20): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(29): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(606): Show |
1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(615): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(56): Show |
1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(65): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(58): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(67): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(18): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(27): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(76): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(85): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(2759): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(2768): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(202): Show |
1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(211): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(312): Show |
1 | a0001c0009t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(321): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(786): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(795): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289847
|
G | GTCTCTGC others(54): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(63): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289847 | |||||
| chr1:1289848
|
T | C | 1 | a0002c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1663-423T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289848 | ||||||
| chr1:1289848
|
T | TCCCTGCT others(206): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1663-421_1663-420i others(215): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC | 30 | a0001c0001t0001g0179a0001c0001t0001g0190a0001c0001t0001g0204others(27): Show | 30 | HG00423.hp1 HG01069.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1663-422_1663-421i others(9): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(20): Show |
2 | a0002c0002t0001g0023a0002c0002t0001g0094 | 2 | HG02004.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1663-422_1663-421i others(29): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(374): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(383): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(18): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(27): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(166): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(175): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(130): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(139): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(54): Show |
1 | a0001c0001t0005g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(63): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(74): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(83): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(112): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(121): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(38): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(47): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCC others(1262): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-422_1663-421i others(1271): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCT others(838): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(847): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCT others(566): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(575): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCT others(430): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(439): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCT others(290): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(299): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCT others(36): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(45): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289848
|
T | TCTCTGCT others(220): Show |
1 | a0001c0018t0005g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1663-422_1663-421i others(229): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289848 | |||||
| chr1:1289850
|
C | CCTGCCCC others(7): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-421_1663-420i others(16): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289850 | ||||||
| chr1:1289850
|
C | T | 37 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0177others(34): Show | 37 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1663-421C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289850 | ||||||
| chr1:1289850
|
CGTCCCCC others(6): Show |
C | 1 | a0002c0002t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1663-420_1663-408d others(15): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289850 | ||||||
| chr1:1289851
|
G | A | 6 | a0002c0002t0001g0030a0002c0002t0001g0067a0002c0002t0001g0084others(3): Show | 6 | HG01243.hp1 HG03927.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-420G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289851 | ||||||
| chr1:1289851
|
G | C | 50 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(47): Show | 50 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1663-420G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289851 | ||||||
| chr1:1289852
|
T | C | 1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-419T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289852 | ||||||
| chr1:1289853
|
C | G | 50 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(47): Show | 50 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1663-418C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289853 | ||||||
| chr1:1289853
|
C | T | 5 | a0002c0002t0001g0030a0002c0002t0001g0067a0002c0002t0001g0084others(2): Show | 5 | HG01243.hp1 HG03927.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-418C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289853 | ||||||
| chr1:1289854
|
C | CCCCGT | 14 | a0001c0001t0001g0177a0001c0001t0001g0237a0001c0001t0002g0225others(11): Show | 14 | HG01516.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-413_1663-412i others(7): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCCCGTGT others(211): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1663-413_1663-412i others(220): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCC others(45): Show |
1 | a0001c0001t0001g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1663-416_1663-415i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCT others(9): Show |
2 | a0004c0005t0002g0028a0004c0005t0010g0124 | 2 | HG01169.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1663-416_1663-415i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCT others(1328): Show |
1 | a0005c0016t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1663-416_1663-415i others(1337): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCT others(103): Show |
1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1663-416_1663-415i others(112): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCT others(9): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1663-416_1663-415i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCT others(625): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1663-416_1663-415i others(634): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CCGTGTCT others(267): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-416_1663-415i others(276): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289854 | |||||
| chr1:1289854
|
C | CTCCGT | 36 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(33): Show | 36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1663-417_1663-416i others(7): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289854 | ||||||
| chr1:1289858
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663-413G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289858 | ||||||
| chr1:1289859
|
A | T | 163 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0166others(160): Show | 163 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1663-412A>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289859 | ||||||
| chr1:1289862
|
C | G | 2 | a0001c0001t0002g0260a0002c0002t0001g0045 | 2 | HG02523.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1663-409C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289862 | ||||||
| chr1:1289863
|
T | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0244a0001c0001t0002g0248others(3): Show | 6 | HG02015.hp2 HG02257.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-408T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289863 | ||||||
| chr1:1289868
|
T | C | 34 | a0001c0001t0001g0177a0001c0001t0001g0194a0001c0001t0001g0201others(31): Show | 34 | HG00438.hp2 HG00639.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1663-403T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289868 | ||||||
| chr1:1289868
|
T | TCCGTCCC others(4698): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1663-360_1663-359i others(4707): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289868 | |||||
| chr1:1289870
|
C | T | 1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-401C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289870 | ||||||
| chr1:1289871
|
G | A | 1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-400G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289871 | ||||||
| chr1:1289872
|
T | TCC | 26 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0001g0179others(23): Show | 26 | HG00642.hp2 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1663-397_1663-396d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289872 | |||||
| chr1:1289872
|
T | TCCCGTGT others(881): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-386_1663-385i others(890): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289872 | |||||
| chr1:1289872
|
T | TCCCGTGT others(13): Show |
1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1663-397_1663-378d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289872 | |||||
| chr1:1289872
|
T | TCCCGTGT others(68): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1663-378_1663-377i others(77): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289872 | |||||
| chr1:1289876
|
G | A | 1 | a0001c0009t0001g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1663-395G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289876 | ||||||
| chr1:1289877
|
T | A | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1663-394T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289877 | ||||||
| chr1:1289881
|
T | C | 7 | a0001c0001t0001g0175a0001c0001t0001g0242a0002c0002t0001g0108others(4): Show | 7 | HG01361.hp2 HG02922.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-390T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289881 | ||||||
| chr1:1289886
|
T | C | 35 | a0001c0001t0001g0160a0001c0001t0001g0194a0001c0001t0001g0195others(32): Show | 35 | HG00621.hp2 HG01175.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1663-385T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289886 | ||||||
| chr1:1289888
|
C | T | 2 | a0003c0004t0003g0106a0003c0004t0003g0171 | 2 | HG02300.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1663-383C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289888 | ||||||
| chr1:1289889
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1663-382G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289889 | ||||||
| chr1:1289889
|
G | C | 1 | a0002c0002t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1663-382G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289889 | ||||||
| chr1:1289890
|
T | TCC | 18 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0202others(15): Show | 18 | HG01070.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-379_1663-378d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289890 | |||||
| chr1:1289890
|
T | TCCCCCGT others(53): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1663-378_1663-377i others(62): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289890 | |||||
| chr1:1289890
|
T | TCCCCCGT others(15): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1663-378_1663-377i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289890 | |||||
| chr1:1289890
|
T | TCCCGTGT others(215): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1663-350_1663-349i others(224): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289890 | |||||
| chr1:1289892
|
CCGTGTCT others(9): Show |
C | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1663-377_1663-362d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289892 | |||||
| chr1:1289894
|
G | C | 1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-377G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289894 | ||||||
| chr1:1289895
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1663-376T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289895 | ||||||
| chr1:1289895
|
T | C | 1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-376T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289895 | ||||||
| chr1:1289895
|
T | TGTCTCTG others(33): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-360_1663-359i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289895 | |||||
| chr1:1289898
|
C | G | 1 | a0002c0002t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1663-373C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289898 | ||||||
| chr1:1289899
|
T | C | 15 | a0001c0001t0001g0175a0001c0001t0001g0207a0001c0001t0001g0242others(12): Show | 15 | HG01361.hp2 HG02015.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663-372T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289899 | ||||||
| chr1:1289904
|
T | C | 41 | a0001c0001t0001g0160a0001c0001t0001g0178a0001c0001t0001g0186others(38): Show | 41 | HG00423.hp1 HG00558.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1663-367T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289904 | ||||||
| chr1:1289907
|
G | A | 4 | a0002c0002t0001g0034a0002c0002t0001g0068a0003c0004t0003g0142others(1): Show | 4 | HG00558.hp2 HG01081.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-364G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289907 | ||||||
| chr1:1289908
|
T | TCC | 14 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0213others(11): Show | 14 | HG01258.hp1 HG01346.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-361_1663-360d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCCCGT others(15): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1663-360_1663-359i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCCCGT others(33): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1663-360_1663-359i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCCCGT others(179): Show |
1 | a0002c0003t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1663-360_1663-359i others(188): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCCCGT others(161): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1663-360_1663-359i others(170): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCGTGT others(13): Show |
1 | a0002c0003t0002g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1663-349_1663-330d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCGTGT others(273): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1663-330_1663-329i others(282): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TCCCGTGT others(51): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1663-350_1663-349i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289908 | |||||
| chr1:1289908
|
T | TTC | 4 | a0002c0002t0001g0034a0002c0002t0001g0068a0003c0004t0003g0142others(1): Show | 4 | HG00558.hp2 HG01081.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-363_1663-362i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289908 | ||||||
| chr1:1289910
|
CCGTGTCT others(83): Show |
C | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1663-359_1663-270d others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289910 | |||||
| chr1:1289910
|
CCGTGTCT others(101): Show |
C | 3 | a0002c0002t0001g0011a0002c0002t0001g0036a0019c0026t0001g0014 | 3 | HG00408.hp2 HG03490.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1663-359_1663-252d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289910 | |||||
| chr1:1289912
|
G | A | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663-359G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289912 | ||||||
| chr1:1289912
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663-359G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289912 | ||||||
| chr1:1289913
|
T | A | 4 | a0001c0001t0002g0169a0001c0012t0001g0127a0001c0012t0001g0131others(1): Show | 4 | HG00408.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-358T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289913 | ||||||
| chr1:1289913
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663-358T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289913 | ||||||
| chr1:1289916
|
CTCTGCCC others(49): Show |
C | 1 | a0008c0007t0004g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1663-349_1663-294d others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289916 | |||||
| chr1:1289917
|
T | C | 4 | a0001c0001t0001g0178a0002c0002t0001g0045a0002c0002t0001g0102others(1): Show | 4 | HG01081.hp1 NA18947.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-354T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289917 | ||||||
| chr1:1289922
|
C | CCCGTCCC others(395): Show |
1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(404): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289922 | |||||
| chr1:1289922
|
C | T | 132 | a0001c0001t0001g0162a0001c0001t0001g0178a0001c0001t0001g0179others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1663-349C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289922 | ||||||
| chr1:1289924
|
C | T | 2 | a0001c0046t0001g0259a0002c0002t0001g0085 | 2 | HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1663-347C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289924 | ||||||
| chr1:1289925
|
G | A | 15 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0065others(12): Show | 15 | HG00621.hp1 HG01069.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663-346G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289925 | ||||||
| chr1:1289926
|
TCC | T | 62 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0178others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1663-341_1663-340d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289926 | |||||
| chr1:1289927
|
C | CCCGTGTC others(49): Show |
1 | a0002c0002t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289927 | |||||
| chr1:1289927
|
C | T | 15 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0065others(12): Show | 15 | HG00621.hp1 HG01069.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663-344C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289927 | ||||||
| chr1:1289927
|
CCCCCGTG others(84): Show |
C | 1 | a0002c0003t0005g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1663-340_1663-250d others(93): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289927 | |||||
| chr1:1289928
|
C | CCCCGTGT others(31): Show |
1 | a0002c0003t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1663-330_1663-329i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCCCGTGT others(49): Show |
1 | a0002c0003t0002g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1663-330_1663-329i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCCCGTGT others(49): Show |
1 | a0002c0003t0004g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1663-330_1663-329i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCCCGTGT others(393): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-330_1663-329i others(402): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCCCGTGT others(343): Show |
1 | a0002c0003t0002g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1663-304_1663-303i others(352): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCC others(123): Show |
1 | a0001c0001t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCC others(467): Show |
1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(476): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(67): Show |
1 | a0002c0002t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(119): Show |
1 | a0002c0003t0002g0074 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(128): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(47): Show |
2 | a0001c0001t0002g0140a0001c0001t0002g0236 | 2 | HG02135.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1663-342_1663-341i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(159): Show |
1 | a0004c0005t0002g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(85): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(94): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(153): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(162): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(65): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(30): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(39): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0023 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(9): Show |
3 | a0001c0001t0001g0193a0001c0001t0002g0249a0002c0003t0002g0061 | 3 | HG01175.hp1 HG03017.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1663-342_1663-341i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(49): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(729): Show |
1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(738): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(47): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(761): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(770): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(99): Show |
1 | a0001c0001t0001g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(108): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(45): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(269): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-342_1663-341i others(278): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CCGTGTCT others(25): Show |
1 | a0025c0044t0003g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1663-342_1663-341i others(34): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289928 | |||||
| chr1:1289928
|
C | CTGTGTCT others(67): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1663-343_1663-342i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289928 | ||||||
| chr1:1289932
|
G | A | 1 | a0003c0004t0003g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1663-339G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289932 | ||||||
| chr1:1289933
|
T | A | 2 | a0001c0001t0002g0231a0013c0042t0001g0129 | 2 | NA19004.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1663-338T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289933 | ||||||
| chr1:1289933
|
T | TGTCTCTG others(11): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-321_1663-320i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289933 | |||||
| chr1:1289934
|
GTC | G | 3 | a0001c0001t0001g0207a0002c0002t0001g0109a0004c0008t0001g0262 | 3 | HG03579.hp1 HG03579.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1663-333_1663-332d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289934 | |||||
| chr1:1289936
|
C | CTGCTCCG others(29): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-334_1663-333i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289936 | |||||
| chr1:1289937
|
T | C | 9 | a0001c0001t0001g0185a0001c0001t0001g0237a0001c0001t0001g0238others(6): Show | 9 | HG00544.hp2 HG00673.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1663-334T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289937 | ||||||
| chr1:1289937
|
T | TCTGCTCC others(429): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-304_1663-303i others(438): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289937 | |||||
| chr1:1289942
|
T | C | 37 | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0001t0001g0202others(34): Show | 37 | HG00099.hp2 HG00558.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1663-329T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289942 | ||||||
| chr1:1289945
|
G | A | 5 | a0002c0002t0001g0084a0002c0002t0001g0089a0004c0008t0001g0239others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-326G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289945 | ||||||
| chr1:1289946
|
T | TCC | 24 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0198others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.1663-323_1663-322d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289946 | |||||
| chr1:1289946
|
T | TCCCCCGT others(619): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1663-322_1663-321i others(628): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289946 | |||||
| chr1:1289946
|
TCCCGTGT others(175): Show |
T | 4 | a0002c0002t0001g0025a0002c0002t0001g0077a0002c0002t0013g0075others(1): Show | 4 | HG00423.hp2 HG02300.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-303_1663-122d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289946 | |||||
| chr1:1289947
|
C | T | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1663-324C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289947 | ||||||
| chr1:1289948
|
CCGTGTCT others(63): Show |
C | 3 | a0002c0002t0001g0003a0002c0002t0001g0053a0002c0003t0002g0082 | 3 | HG00438.hp2 HG02683.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1663-321_1663-252d others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289948 | |||||
| chr1:1289948
|
CCGTGTCT others(81): Show |
C | 1 | a0002c0002t0001g0089 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1663-321_1663-234d others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289948 | |||||
| chr1:1289948
|
CCGTGTCT others(99): Show |
C | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1663-321_1663-216d others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289948 | |||||
| chr1:1289950
|
G | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0189 | 2 | HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1663-321G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289950 | ||||||
| chr1:1289951
|
T | A | 1 | a0001c0001t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1663-320T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289951 | ||||||
| chr1:1289951
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0189 | 2 | HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1663-320T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289951 | ||||||
| chr1:1289954
|
C | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0189 | 2 | HG01361.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1663-317C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289954 | ||||||
| chr1:1289954
|
CTCTGCTC others(11): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1663-303_1663-286d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289954 | |||||
| chr1:1289955
|
T | C | 2 | a0002c0003t0002g0083a0004c0008t0001g0262 | 2 | HG03579.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1663-316T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289955 | ||||||
| chr1:1289955
|
TCTGCTCC others(47): Show |
T | 4 | a0002c0002t0001g0052a0002c0002t0001g0059a0002c0002t0001g0085others(1): Show | 4 | HG00544.hp1 HG02976.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-303_1663-250d others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289955 | |||||
| chr1:1289955
|
TCTGCTCC others(83): Show |
T | 2 | a0002c0002t0001g0035a0002c0002t0001g0067 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1663-303_1663-214d others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289955 | |||||
| chr1:1289955
|
TCTGCTCC others(211): Show |
T | 1 | a0005c0011t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1663-303_1663-86de others(1): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289955 | |||||
| chr1:1289960
|
T | C | 32 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0002g0161others(29): Show | 32 | HG00673.hp1 HG01070.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1663-311T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289960 | ||||||
| chr1:1289963
|
G | A | 7 | a0001c0012t0001g0127a0001c0012t0001g0131a0002c0002t0001g0017others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-308G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289963 | ||||||
| chr1:1289965
|
C | T | 6 | a0001c0012t0001g0127a0001c0012t0001g0131a0002c0002t0001g0017others(3): Show | 6 | HG01516.hp1 HG01517.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-306C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289965 | ||||||
| chr1:1289966
|
C | CCGTGTCT others(29): Show |
1 | a0001c0018t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1663-304_1663-303i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289966 | |||||
| chr1:1289966
|
C | CCGTGTCT others(9): Show |
1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1663-304_1663-303i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289966 | |||||
| chr1:1289966
|
C | CCGTGTCT others(159): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1663-304_1663-303i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289966 | |||||
| chr1:1289966
|
C | CCGTGTCT others(27): Show |
1 | a0020c0030t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1663-304_1663-303i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289966 | |||||
| chr1:1289966
|
CCCCGTGT others(45): Show |
C | 8 | a0002c0002t0001g0031a0002c0002t0001g0037a0002c0002t0001g0058others(5): Show | 8 | HG00621.hp2 HG03688.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-295_1663-244d others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289966 | |||||
| chr1:1289966
|
CCCCGTGT others(81): Show |
C | 4 | a0002c0002t0001g0010a0003c0004t0003g0005a0003c0004t0003g0139others(1): Show | 4 | NA19007.hp2 NA19070.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-295_1663-208d others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289966 | |||||
| chr1:1289968
|
C | G | 88 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0178others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1663-303C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289968 | ||||||
| chr1:1289969
|
C | A | 1 | a0001c0001t0002g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1663-302C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289969 | ||||||
| chr1:1289969
|
C | T | 88 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0178others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1663-302C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289969 | ||||||
| chr1:1289972
|
G | C | 90 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0178others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1663-299G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289972 | ||||||
| chr1:1289972
|
G | GTC | 52 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0200others(49): Show | 52 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.1663-297_1663-296d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCCCTGC others(167): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-297_1663-296i others(176): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(651): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(660): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(49): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(58): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(239): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(248): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(275): Show |
1 | a0002c0002t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(284): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(13): Show |
1 | a0003c0004t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(129): Show |
1 | a0007c0006t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(138): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(15): Show |
1 | a0002c0003t0004g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(2369): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(2378): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(87): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(439): Show |
1 | a0005c0016t0001g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(448): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(51): Show |
1 | a0002c0002t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(685): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(694): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(333): Show |
1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-296_1663-295i others(342): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(519): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(528): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTCTGC others(143): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289972
|
G | GTCTGCTC others(29): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-281_1663-280i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289972 | |||||
| chr1:1289973
|
T | C | 10 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0178others(7): Show | 10 | HG00735.hp1 HG01081.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-298T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289973 | ||||||
| chr1:1289973
|
T | TCCCTGCT others(201): Show |
1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1663-297_1663-296i others(210): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289973 | |||||
| chr1:1289973
|
T | TCTCTGCC others(325): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(334): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289973 | |||||
| chr1:1289973
|
T | TCTCTGCT others(67): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663-296_1663-295i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289973 | |||||
| chr1:1289975
|
TGCTCCGT others(9): Show |
T | 5 | a0002c0003t0002g0027a0002c0003t0004g0116a0004c0005t0002g0022others(2): Show | 5 | HG00738.hp1 HG01123.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-295_1663-280d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289975 | ||||||
| chr1:1289975
|
TGCTCCGT others(27): Show |
T | 2 | a0003c0004t0003g0148a0006c0010t0007g0273 | 2 | HG00597.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1663-295_1663-262d others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289975 | ||||||
| chr1:1289975
|
TGCTCCGT others(63): Show |
T | 4 | a0002c0002t0001g0030a0003c0004t0003g0133a0003c0004t0003g0135others(1): Show | 4 | NA18964.hp2 NA18998.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-295_1663-226d others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289975 | ||||||
| chr1:1289978
|
T | C | 19 | a0001c0001t0001g0179a0001c0047t0001g0183a0002c0002t0001g0094others(16): Show | 19 | HG00099.hp2 HG01175.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1663-293T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289978 | ||||||
| chr1:1289981
|
G | A | 4 | a0001c0001t0001g0196a0002c0002t0001g0042a0002c0002t0001g0080others(1): Show | 4 | HG02523.hp2 NA19012.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-290G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289981 | ||||||
| chr1:1289982
|
T | TCC | 22 | a0001c0001t0001g0181a0001c0001t0001g0187a0001c0001t0001g0192others(19): Show | 22 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1663-287_1663-286d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289982 | |||||
| chr1:1289982
|
T | TCCCCCGT others(143): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1663-286_1663-285i others(152): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289982 | |||||
| chr1:1289982
|
T | TCCCGTGT others(31): Show |
2 | a0002c0003t0002g0012a0002c0003t0002g0104 | 2 | HG01257.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1663-281_1663-280i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289982 | |||||
| chr1:1289982
|
T | TCCCGTGT others(182): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-281_1663-280i others(191): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289982 | |||||
| chr1:1289982
|
T | TTC | 3 | a0002c0002t0001g0042a0002c0002t0001g0080a0013c0042t0001g0129 | 3 | HG02523.hp2 NA19012.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1663-289_1663-288i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289982 | ||||||
| chr1:1289984
|
CCGTGTCC others(9): Show |
C | 3 | a0003c0004t0003g0150a0004c0008t0001g0241a0008c0007t0004g0266 | 3 | HG01109.hp1 HG02071.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1663-285_1663-270d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289984 | |||||
| chr1:1289984
|
CCGTGTCC others(63): Show |
C | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1663-285_1663-216d others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289984 | |||||
| chr1:1289986
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-285G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289986 | ||||||
| chr1:1289987
|
T | A | 5 | a0001c0001t0002g0249a0003c0004t0003g0142a0003c0004t0003g0144others(2): Show | 5 | HG00558.hp2 HG02074.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-284T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289987 | ||||||
| chr1:1289987
|
T | TGTCTCTG others(31): Show |
1 | a0002c0002t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1663-281_1663-280i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289987 | |||||
| chr1:1289990
|
C | CTCTGCTC others(9): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1663-281_1663-280i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289990 | ||||||
| chr1:1289991
|
C | CCTGCTCC others(33): Show |
1 | a0002c0003t0004g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-268_1663-267i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289991 | |||||
| chr1:1289991
|
C | T | 137 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0182others(134): Show | 137 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1663-280C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289991 | ||||||
| chr1:1289996
|
T | C | 22 | a0001c0001t0002g0233a0001c0001t0011g0268a0002c0002t0001g0029others(19): Show | 22 | HG00423.hp1 HG00673.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1663-275T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289996 | ||||||
| chr1:1289996
|
T | TCCGTCCC others(1855): Show |
1 | a0002c0003t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1663-268_1663-267i others(1864): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289996 | |||||
| chr1:1289996
|
T | TCCGTCCC others(87): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1663-263_1663-262i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1289996 | |||||
| chr1:1289998
|
C | T | 2 | a0006c0010t0007g0270a0006c0010t0007g0274 | 2 | HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1663-273C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289998 | ||||||
| chr1:1289999
|
G | A | 8 | a0001c0001t0002g0260a0002c0002t0001g0023a0002c0002t0001g0034others(5): Show | 8 | HG01081.hp2 HG01952.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-272G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1289999 | ||||||
| chr1:1290000
|
T | TCC | 27 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0193others(24): Show | 27 | HG00408.hp1 HG01070.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1663-269_1663-268d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290000 | |||||
| chr1:1290000
|
T | TCCCGTGT others(123): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1663-263_1663-262i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290000 | |||||
| chr1:1290000
|
T | TTC | 7 | a0002c0002t0001g0023a0002c0002t0001g0034a0002c0002t0001g0049others(4): Show | 7 | HG01081.hp2 HG01952.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-271_1663-270i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290000 | ||||||
| chr1:1290002
|
CCGTGTCC others(9): Show |
C | 2 | a0002c0002t0001g0016a0009c0013t0001g0078 | 2 | NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1663-267_1663-252d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290002 | |||||
| chr1:1290002
|
CCGTGTCC others(63): Show |
C | 1 | a0004c0008t0001g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1663-267_1663-198d others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290002 | |||||
| chr1:1290002
|
CCGTGTCC others(81): Show |
C | 1 | a0004c0008t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1663-267_1663-180d others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290002 | |||||
| chr1:1290004
|
G | A | 1 | a0001c0036t0006g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1663-267G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290004 | ||||||
| chr1:1290005
|
T | A | 3 | a0001c0001t0001g0246a0001c0001t0002g0169a0003c0004t0003g0150 | 3 | HG00408.hp1 HG02071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1663-266T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290005 | ||||||
| chr1:1290009
|
C | CCTGCTCC others(665): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1663-250_1663-249i others(674): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290009 | |||||
| chr1:1290009
|
C | CCTGCTCC others(851): Show |
1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1663-155_1663-154i others(860): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290009 | |||||
| chr1:1290009
|
C | T | 146 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(143): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1663-262C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290009 | ||||||
| chr1:1290009
|
CCTGCTCC others(11): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1663-244_1663-227d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290009 | |||||
| chr1:1290014
|
T | C | 20 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0207others(17): Show | 20 | HG01109.hp1 HG01516.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-257T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290014 | ||||||
| chr1:1290017
|
G | A | 4 | a0002c0002t0001g0068a0002c0002t0001g0079a0002c0003t0001g0112others(1): Show | 4 | HG02155.hp2 HG02559.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-254G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290017 | ||||||
| chr1:1290018
|
T | TCC | 17 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0207others(14): Show | 17 | HG00423.hp1 HG00544.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-251_1663-250d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TCCCCCGT others(449): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-250_1663-249i others(458): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TCCCCCGT others(35): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1663-250_1663-249i others(44): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TCCCCCGT others(417): Show |
1 | a0002c0003t0002g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-250_1663-249i others(426): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TCCCCCGT others(549): Show |
1 | a0015c0037t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-250_1663-249i others(558): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TCCCCCGT others(107): Show |
1 | a0001c0001t0001g0252 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1663-250_1663-249i others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TCCCGTGT others(51): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-237_1663-236i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290018 | |||||
| chr1:1290018
|
T | TTC | 4 | a0002c0002t0001g0068a0002c0002t0001g0079a0002c0003t0001g0112others(1): Show | 4 | HG02155.hp2 HG02559.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-253_1663-252i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290018 | ||||||
| chr1:1290020
|
CCGTGTCT others(9): Show |
C | 1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1663-249_1663-234d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290020 | |||||
| chr1:1290022
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1663-249G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290022 | ||||||
| chr1:1290022
|
G | C | 1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-249G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290022 | ||||||
| chr1:1290023
|
T | A | 6 | a0001c0001t0001g0178a0001c0001t0001g0242a0001c0001t0002g0173others(3): Show | 6 | HG01081.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-248T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290023 | ||||||
| chr1:1290023
|
T | C | 1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-248T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290023 | ||||||
| chr1:1290026
|
C | G | 1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-245C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290026 | ||||||
| chr1:1290027
|
T | C | 22 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0194others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1663-244T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290027 | ||||||
| chr1:1290027
|
T | TCTGCTCC others(9352): Show |
1 | a0001c0001t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1663-227_1663-226i others(9361): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290027 | |||||
| chr1:1290027
|
TCTGCTCC others(11): Show |
T | 1 | a0001c0020t0001g0176 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1663-226_1663-209d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290027 | |||||
| chr1:1290032
|
T | C | 21 | a0001c0001t0001g0162a0001c0001t0001g0193a0001c0001t0002g0169others(18): Show | 21 | HG00099.hp2 HG00408.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1663-239T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290032 | ||||||
| chr1:1290032
|
T | TCCGTCCC others(13): Show |
1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1663-232_1663-231i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290032 | |||||
| chr1:1290035
|
G | A | 3 | a0002c0002t0001g0029a0002c0002t0001g0046a0002c0002t0001g0094 | 3 | HG00423.hp1 HG02015.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1663-236G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290035 | ||||||
| chr1:1290036
|
T | TCC | 34 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0001t0001g0213others(31): Show | 34 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1663-233_1663-232d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290036 | |||||
| chr1:1290036
|
T | TCCCCCGT others(15): Show |
1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1663-232_1663-231i others(24): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290036 | |||||
| chr1:1290036
|
T | TCCCGTGT others(51): Show |
1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1663-214_1663-213i others(60): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290036 | |||||
| chr1:1290036
|
T | TCCCGTGT others(31): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-227_1663-226i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290036 | |||||
| chr1:1290036
|
T | TTCCCCGT others(87): Show |
1 | a0002c0002t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1663-235_1663-234i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290036 | ||||||
| chr1:1290038
|
CCGTGTCC others(9): Show |
C | 1 | a0003c0004t0003g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1663-231_1663-216d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290038 | |||||
| chr1:1290040
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-231G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290040 | ||||||
| chr1:1290040
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1663-231G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290040 | ||||||
| chr1:1290041
|
T | A | 4 | a0002c0003t0002g0015a0003c0004t0003g0141a0004c0008t0001g0241others(1): Show | 4 | HG01109.hp1 HG03491.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-230T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290041 | ||||||
| chr1:1290041
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1663-230T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290041 | ||||||
| chr1:1290041
|
T | TGTCTCTG others(1607): Show |
1 | a0002c0003t0001g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1663-227_1663-226i others(1616): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290041 | |||||
| chr1:1290044
|
C | CTGCTCCG others(1355): Show |
1 | a0002c0003t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1663-227_1663-226i others(1364): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290044 | ||||||
| chr1:1290044
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1663-227C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290044 | ||||||
| chr1:1290045
|
C | CCTGCTCC others(11): Show |
2 | a0001c0001t0001g0203a0002c0003t0002g0099 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1663-159_1663-142d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290045 | |||||
| chr1:1290045
|
C | T | 171 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0167others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1663-226C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290045 | ||||||
| chr1:1290045
|
CCTGCTCC others(11): Show |
C | 2 | a0001c0001t0001g0212a0001c0001t0001g0214 | 2 | HG00642.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1663-159_1663-142d others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290045 | |||||
| chr1:1290050
|
T | C | 27 | a0001c0001t0001g0166a0001c0001t0001g0193a0001c0001t0001g0198others(24): Show | 27 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1663-221T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290050 | ||||||
| chr1:1290052
|
C | CGTCCCCC others(2953): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-214_1663-213i others(2962): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290052 | |||||
| chr1:1290052
|
C | T | 1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-219C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290052 | ||||||
| chr1:1290053
|
G | A | 4 | a0002c0002t0001g0045a0002c0003t0001g0018a0007c0006t0001g0070others(1): Show | 4 | HG01243.hp1 HG02738.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-218G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290053 | ||||||
| chr1:1290054
|
T | TCC | 30 | a0001c0001t0001g0197a0001c0001t0001g0207a0001c0001t0001g0213others(27): Show | 30 | HG00642.hp1 HG01175.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1663-215_1663-214d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290054 | |||||
| chr1:1290054
|
T | TCCCCCGT others(545): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1663-214_1663-213i others(554): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290054 | |||||
| chr1:1290054
|
T | TCCCGTGT others(233): Show |
1 | a0001c0001t0001g0162 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1663-204_1663-203i others(242): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290054 | |||||
| chr1:1290054
|
T | TCCCGTGT others(87): Show |
1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1663-204_1663-203i others(96): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290054 | |||||
| chr1:1290054
|
T | TCCCGTGT others(33): Show |
2 | a0008c0007t0004g0284a0008c0007t0004g0285 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1663-196_1663-195i others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290054 | |||||
| chr1:1290054
|
T | TTC | 3 | a0002c0002t0001g0045a0002c0003t0001g0018a0007c0006t0001g0070 | 3 | HG01243.hp1 HG02738.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1663-217_1663-216i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290054 | ||||||
| chr1:1290055
|
C | T | 1 | a0016c0031t0001g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1663-216C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290055 | ||||||
| chr1:1290056
|
CCGTGTCT others(9): Show |
C | 2 | a0002c0003t0002g0083a0016c0031t0001g0092 | 2 | HG04204.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1663-213_1663-198d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290056 | |||||
| chr1:1290058
|
G | C | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-213G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290058 | ||||||
| chr1:1290059
|
T | A | 12 | a0001c0001t0001g0197a0001c0001t0001g0207a0001c0001t0002g0228others(9): Show | 12 | HG01175.hp2 HG02109.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.1663-212T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290059 | ||||||
| chr1:1290059
|
T | C | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-212T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290059 | ||||||
| chr1:1290062
|
C | G | 1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-209C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290062 | ||||||
| chr1:1290063
|
T | C | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0181others(17): Show | 20 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-208T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290063 | ||||||
| chr1:1290063
|
T | TCTGCTCC others(177): Show |
1 | a0001c0001t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1663-196_1663-195i others(186): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290063 | |||||
| chr1:1290068
|
T | C | 23 | a0001c0001t0001g0162a0001c0001t0001g0192a0001c0001t0001g0193others(20): Show | 23 | HG00735.hp1 HG01433.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1663-203T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290068 | ||||||
| chr1:1290070
|
C | T | 5 | a0002c0003t0002g0081a0003c0004t0003g0005a0003c0004t0003g0139others(2): Show | 5 | HG03688.hp2 NA18967.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-201C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290070 | ||||||
| chr1:1290071
|
G | A | 3 | a0002c0002t0001g0031a0002c0002t0001g0047a0002c0002t0001g0052 | 3 | HG00544.hp1 HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1663-200G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290071 | ||||||
| chr1:1290072
|
T | TCC | 19 | a0001c0001t0001g0179a0001c0001t0001g0242a0001c0001t0001g0246others(16): Show | 19 | HG00438.hp1 HG01069.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1663-197_1663-196d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290072 | |||||
| chr1:1290072
|
T | TCCCCCGT others(157): Show |
1 | a0001c0001t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-196_1663-195i others(166): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290072 | |||||
| chr1:1290072
|
T | TCCCGTGT others(215): Show |
1 | a0001c0001t0001g0204 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1663-104_1663-103i others(224): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290072 | |||||
| chr1:1290072
|
TCCCGTGT others(49): Show |
T | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1663-154_1663-99de others(57): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290072 | |||||
| chr1:1290073
|
C | T | 1 | a0002c0002t0001g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1663-198C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290073 | ||||||
| chr1:1290074
|
CCGTGTCT others(27): Show |
C | 2 | a0002c0002t0001g0052a0002c0002t0001g0059 | 2 | HG00544.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1663-195_1663-162d others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290074 | |||||
| chr1:1290076
|
G | A | 1 | a0002c0002t0001g0086 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1663-195G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290076 | ||||||
| chr1:1290076
|
G | C | 3 | a0005c0011t0001g0156a0005c0011t0001g0157a0018c0027t0001g0020 | 3 | HG02622.hp2 HG02895.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1663-195G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290076 | ||||||
| chr1:1290077
|
T | A | 8 | a0001c0001t0002g0140a0001c0001t0002g0230a0001c0001t0002g0236others(5): Show | 8 | HG01928.hp1 HG02015.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663-194T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290077 | ||||||
| chr1:1290077
|
T | C | 3 | a0005c0011t0001g0156a0005c0011t0001g0157a0018c0027t0001g0020 | 3 | HG02622.hp2 HG02895.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1663-194T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290077 | ||||||
| chr1:1290077
|
T | TGTCCCTG others(31): Show |
3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG02257.hp1 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1663-191_1663-190i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290077 | |||||
| chr1:1290080
|
C | G | 3 | a0005c0011t0001g0156a0005c0011t0001g0157a0018c0027t0001g0020 | 3 | HG02622.hp2 HG02895.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1663-191C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290080 | ||||||
| chr1:1290081
|
T | C | 20 | a0001c0001t0001g0175a0001c0001t0001g0193a0001c0001t0001g0222others(17): Show | 20 | HG00558.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-190T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290081 | ||||||
| chr1:1290086
|
T | C | 25 | a0001c0001t0001g0198a0001c0001t0001g0213a0001c0001t0001g0217others(22): Show | 25 | HG00673.hp1 HG00673.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1663-185T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290086 | ||||||
| chr1:1290089
|
G | A | 7 | a0002c0002t0001g0013a0002c0002t0001g0049a0002c0002t0001g0085others(4): Show | 7 | HG01943.hp1 HG01952.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-182G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290089 | ||||||
| chr1:1290090
|
T | TCC | 27 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0200others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.1663-179_1663-178d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290090 | |||||
| chr1:1290090
|
T | TCCCCCGT others(165): Show |
1 | a0007c0006t0001g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1663-178_1663-177i others(174): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290090 | |||||
| chr1:1290090
|
T | TCCCCCGT others(73): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-178_1663-177i others(82): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290090 | |||||
| chr1:1290090
|
T | TCCCGTGT others(395): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-168_1663-167i others(404): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290090 | |||||
| chr1:1290090
|
T | TTC | 6 | a0002c0002t0001g0013a0002c0002t0001g0049a0002c0002t0001g0085others(3): Show | 6 | HG01943.hp1 HG01952.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-181_1663-180i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290090 | ||||||
| chr1:1290092
|
CCGTGTCT others(9): Show |
C | 6 | a0001c0001t0011g0268a0002c0002t0001g0057a0002c0002t0001g0062others(3): Show | 6 | HG00673.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-177_1663-162d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290092 | |||||
| chr1:1290094
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1663-177G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290094 | ||||||
| chr1:1290095
|
T | A | 4 | a0001c0001t0002g0173a0001c0036t0006g0123a0004c0008t0001g0239others(1): Show | 4 | HG01993.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-176T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290095 | ||||||
| chr1:1290095
|
T | TGTCCCTG others(13): Show |
1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1663-173_1663-172i others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290095 | |||||
| chr1:1290095
|
T | TGTCCCTG others(107): Show |
1 | a0001c0020t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1663-173_1663-172i others(116): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290095 | |||||
| chr1:1290096
|
GTCTCTGC others(33): Show |
G | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1663-171_1663-132d others(42): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290096 | |||||
| chr1:1290099
|
T | C | 23 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0200others(20): Show | 23 | HG00544.hp2 HG01069.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1663-172T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290099 | ||||||
| chr1:1290099
|
TCTGCTCC others(67): Show |
T | 1 | a0002c0002t0001g0095 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1663-154_1663-81de others(75): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290099 | |||||
| chr1:1290104
|
T | C | 33 | a0001c0001t0002g0230a0001c0001t0002g0248a0002c0002t0001g0003others(30): Show | 33 | HG00408.hp2 HG00438.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.1663-167T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290104 | ||||||
| chr1:1290104
|
TCCGTCCC others(68): Show |
T | 1 | a0022c0040t0012g0159 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1663-165_1663-91de others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290104 | |||||
| chr1:1290106
|
C | T | 1 | a0001c0046t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1663-165C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290106 | ||||||
| chr1:1290107
|
G | A | 4 | a0003c0004t0003g0141a0006c0010t0007g0275a0015c0037t0001g0090others(1): Show | 4 | HG03490.hp2 HG03540.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-164G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290107 | ||||||
| chr1:1290108
|
T | TCC | 43 | a0001c0001t0001g0179a0001c0001t0001g0187a0001c0001t0001g0213others(40): Show | 43 | HG00408.hp2 HG00438.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1663-161_1663-160d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290108 | |||||
| chr1:1290108
|
T | TCCCGTGT others(31): Show |
1 | a0002c0003t0004g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1663-150_1663-149i others(40): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290108 | |||||
| chr1:1290108
|
T | TTC | 3 | a0003c0004t0003g0141a0015c0037t0001g0090a0019c0026t0001g0014 | 3 | HG03490.hp2 HG03540.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1663-163_1663-162i others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290108 | ||||||
| chr1:1290108
|
TCCCGTGT others(13): Show |
T | 5 | a0002c0002t0001g0031a0002c0002t0001g0047a0002c0028t0001g0093others(2): Show | 5 | HG00621.hp2 HG00673.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-141_1663-122d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290108 | |||||
| chr1:1290110
|
CCGTGTCT others(29): Show |
C | 2 | a0005c0011t0001g0156a0005c0011t0001g0157 | 2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1663-159_1663-124d others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290110 | |||||
| chr1:1290111
|
C | T | 1 | a0003c0004t0003g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1663-160C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290111 | ||||||
| chr1:1290112
|
G | A | 4 | a0003c0004t0003g0004a0003c0004t0003g0005a0003c0004t0003g0006others(1): Show | 4 | HG01346.hp1 NA18961.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-159G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290112 | ||||||
| chr1:1290113
|
T | A | 1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-158T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290113 | ||||||
| chr1:1290117
|
T | C | 10 | a0001c0001t0001g0186a0001c0001t0001g0237a0001c0001t0002g0230others(7): Show | 10 | HG01891.hp1 HG01928.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1663-154T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290117 | ||||||
| chr1:1290117
|
TCTGCTCC others(49): Show |
T | 2 | a0002c0002t0001g0080a0006c0010t0007g0273 | 2 | HG00597.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1663-141_1663-86de others(57): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290117 | |||||
| chr1:1290117
|
TCTGCTCC others(67): Show |
T | 2 | a0001c0001t0001g0196a0002c0002t0001g0076 | 2 | NA19088.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1663-141_1663-68de others(75): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290117 | |||||
| chr1:1290122
|
T | C | 20 | a0001c0001t0001g0197a0001c0001t0001g0222a0001c0001t0001g0223others(17): Show | 20 | HG00423.hp1 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-149T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290122 | ||||||
| chr1:1290122
|
T | TCCGTCCC others(29): Show |
1 | a0002c0002t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290122 | |||||
| chr1:1290124
|
C | T | 1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-147C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290124 | ||||||
| chr1:1290125
|
G | A | 14 | a0001c0012t0001g0127a0001c0012t0001g0131a0001c0018t0001g0251others(11): Show | 14 | HG00621.hp1 HG01358.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-146G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290125 | ||||||
| chr1:1290126
|
TCC | T | 95 | a0001c0001t0001g0168a0001c0001t0001g0216a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1663-141_1663-140d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290126 | |||||
| chr1:1290127
|
C | T | 12 | a0001c0018t0001g0251a0002c0002t0001g0019a0002c0002t0001g0030others(9): Show | 12 | HG00621.hp1 HG01358.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1663-144C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290127 | ||||||
| chr1:1290128
|
C | CCCCGAGT others(29): Show |
1 | a0002c0003t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-139_1663-138i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGAGT others(199): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1663-139_1663-138i others(208): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGAGT others(123): Show |
1 | a0001c0001t0002g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1663-139_1663-138i others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGAGT others(2387): Show |
1 | a0001c0001t0001g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663-139_1663-138i others(2396): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(11): Show |
1 | a0001c0001t0002g0173 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1663-135_1663-134i others(20): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(109): Show |
1 | a0030c0024t0001g0051 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1663-135_1663-134i others(118): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(145): Show |
1 | a0002c0003t0002g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663-130_1663-129i others(154): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(1053): Show |
1 | a0009c0014t0001g0009 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1663-130_1663-129i others(1062): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(11): Show |
10 | a0001c0001t0001g0213a0001c0001t0001g0217a0001c0018t0001g0251others(7): Show | 10 | HG00423.hp1 HG01934.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1663-116_1663-99du others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(67): Show |
1 | a0001c0001t0002g0248 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1663-112_1663-111i others(76): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(1047): Show |
1 | a0002c0003t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1663-109_1663-108i others(1056): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(65): Show |
1 | a0001c0001t0005g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1663-129_1663-58du others(73): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(67): Show |
2 | a0006c0015t0008g0276a0006c0015t0008g0277 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1663-99_1663-98ins others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCCCGTGT others(103): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-99_1663-98ins others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCC others(65): Show |
1 | a0002c0002t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCC others(139): Show |
1 | a0001c0001t0002g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(148): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCC others(27): Show |
1 | a0003c0004t0003g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCC others(1389): Show |
1 | a0002c0003t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(1398): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(29): Show |
1 | a0003c0004t0003g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(451): Show |
1 | a0010c0019t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(460): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(137): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(473): Show |
1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(482): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(81): Show |
1 | a0010c0019t0003g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(90): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(289): Show |
1 | a0002c0003t0002g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(298): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(181): Show |
1 | a0002c0002t0001g0033 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(190): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(29): Show |
1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(9): Show |
3 | a0002c0002t0001g0045a0003c0004t0003g0134a0007c0006t0001g0071 | 3 | HG03486.hp2 NA18975.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1663-142_1663-141i others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(29): Show |
1 | a0013c0042t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(145): Show |
1 | a0002c0003t0002g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(154): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(163): Show |
1 | a0002c0003t0002g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(172): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(165): Show |
1 | a0007c0006t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(174): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(467): Show |
1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(476): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(121): Show |
1 | a0002c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(130): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(47): Show |
1 | a0001c0001t0002g0236 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(833): Show |
1 | a0001c0001t0002g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(842): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(47): Show |
1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(65): Show |
2 | a0002c0002t0001g0023a0013c0043t0001g0147 | 2 | HG02004.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1663-142_1663-141i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(27): Show |
1 | a0004c0005t0010g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(323): Show |
1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(332): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(47): Show |
1 | a0004c0005t0002g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(159): Show |
1 | a0002c0002t0001g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(168): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(65): Show |
1 | a0002c0002t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(74): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(83): Show |
1 | a0002c0002t0001g0034 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(615): Show |
1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(624): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(157): Show |
1 | a0002c0002t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1663-142_1663-141i others(166): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | CCGTGTCT others(5651): Show |
1 | a0007c0006t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663-142_1663-141i others(5660): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
C | T | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1663-143C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290128 | ||||||
| chr1:1290128
|
CCCCGTGT others(11): Show |
C | 2 | a0001c0001t0001g0242a0004c0008t0001g0247 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1663-116_1663-99de others(19): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290128
|
CCCCGTGT others(29): Show |
C | 1 | a0012c0022t0006g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1663-134_1663-99de others(37): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290128 | |||||
| chr1:1290131
|
C | T | 1 | a0002c0003t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1663-140C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290131 | ||||||
| chr1:1290132
|
G | GTGTCTCT others(635): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1663-130_1663-129i others(644): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290132 | |||||
| chr1:1290132
|
G | T | 1 | a0004c0005t0006g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1663-139G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290132 | ||||||
| chr1:1290133
|
T | A | 1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-138T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290133 | ||||||
| chr1:1290134
|
GTC | G | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0011g0268 | 3 | HG01106.hp2 HG01261.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1663-133_1663-132d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290134 | |||||
| chr1:1290136
|
C | CTCTGCTC others(1166): Show |
1 | a0001c0001t0001g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1663-104_1663-103i others(1175): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290136 | |||||
| chr1:1290137
|
T | C | 4 | a0001c0047t0001g0183a0002c0002t0001g0008a0006c0010t0007g0274others(1): Show | 4 | HG00099.hp2 HG01496.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-134T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290137 | ||||||
| chr1:1290137
|
T | TCTGCTCC others(101): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1663-104_1663-103i others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290137 | |||||
| chr1:1290142
|
T | C | 8 | a0002c0003t0001g0069a0002c0003t0004g0121a0005c0016t0001g0281others(5): Show | 8 | HG01069.hp1 HG01123.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663-129T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290142 | ||||||
| chr1:1290146
|
T | TCC | 20 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(17): Show | 20 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-123_1663-122d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290146 | |||||
| chr1:1290146
|
T | TCCCCCGT others(2721): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-122_1663-121i others(2730): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290146 | |||||
| chr1:1290146
|
T | TCCCCCGT others(105): Show |
1 | a0002c0003t0004g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-122_1663-121i others(114): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290146 | |||||
| chr1:1290146
|
T | TCCCGTGT others(13): Show |
1 | a0002c0003t0004g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1663-123_1663-104d others(22): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290146 | |||||
| chr1:1290148
|
CCGTGTCT others(9): Show |
C | 1 | a0012c0022t0006g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1663-121_1663-106d others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290148 | |||||
| chr1:1290150
|
G | GTGTCTCT others(265): Show |
1 | a0008c0007t0004g0284 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1663-99_1663-98ins others(272): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290150 | |||||
| chr1:1290150
|
G | GTGTCTCT others(265): Show |
1 | a0008c0007t0004g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1663-99_1663-98ins others(272): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290150 | |||||
| chr1:1290150
|
G | T | 2 | a0008c0007t0004g0286a0008c0007t0004g0287 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1663-121G>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290150 | ||||||
| chr1:1290154
|
C | CCCTGCTC others(2377): Show |
1 | a0002c0002t0001g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1663-117_1663-116i others(2386): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290154 | ||||||
| chr1:1290155
|
T | C | 12 | a0002c0002t0001g0013a0002c0002t0001g0023a0002c0002t0001g0031others(9): Show | 12 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1663-116T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290155 | ||||||
| chr1:1290155
|
TCTGCTCC others(11): Show |
T | 4 | a0002c0003t0004g0114a0002c0003t0004g0116a0014c0021t0008g0272others(1): Show | 4 | HG02622.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-80_1663-63del others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290155 | |||||
| chr1:1290158
|
G | A | 8 | a0002c0002t0001g0013a0002c0002t0001g0023a0002c0002t0001g0031others(5): Show | 8 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663-113G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290158 | ||||||
| chr1:1290158
|
G | GCTCCGTC others(29): Show |
1 | a0002c0002t0001g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1663-99_1663-98ins others(36): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290158 | |||||
| chr1:1290158
|
G | GCTCCGTC others(139): Show |
1 | a0026c0041t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-99_1663-98ins others(146): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290158 | |||||
| chr1:1290160
|
T | C | 3 | a0001c0001t0002g0254a0003c0004t0003g0138a0011c0023t0001g0265 | 3 | HG03195.hp1 HG06807.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1663-111T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290160 | ||||||
| chr1:1290163
|
G | C | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1663-108G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290163 | ||||||
| chr1:1290164
|
T | TCC | 5 | a0001c0001t0001g0219a0002c0003t0001g0063a0002c0003t0002g0081others(2): Show | 5 | HG01993.hp1 HG03209.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-105_1663-104d others(4): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290164 | |||||
| chr1:1290164
|
T | TCCCGTGT others(1015): Show |
1 | a0007c0006t0001g0070 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663-99_1663-98ins others(1022): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290164 | |||||
| chr1:1290167
|
C | T | 3 | a0002c0003t0001g0060a0012c0022t0006g0132a0012c0022t0006g0269 | 3 | HG00642.hp1 HG02717.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1663-104C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290167 | ||||||
| chr1:1290168
|
G | A | 2 | a0012c0022t0006g0132a0012c0022t0006g0269 | 2 | HG00642.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1663-103G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290168 | ||||||
| chr1:1290169
|
T | A | 1 | a0003c0004t0003g0138 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-102T>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290169 | ||||||
| chr1:1290173
|
C | CCTACTCC others(11): Show |
1 | a0017c0029t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1663-96_1663-95ins others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(31): Show |
1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1663-91_1663-90ins others(38): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(417): Show |
1 | a0002c0002t0001g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1663-86_1663-85ins others(424): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(399): Show |
1 | a0001c0009t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1663-48_1663-47ins others(406): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(11): Show |
7 | a0002c0003t0002g0012a0002c0003t0002g0021a0002c0003t0002g0027others(4): Show | 7 | HG01123.hp1 HG01255.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-81_1663-80ins others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(47): Show |
1 | a0001c0001t0005g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1663-81_1663-80ins others(54): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(65): Show |
3 | a0001c0001t0002g0232a0001c0001t0005g0226a0001c0018t0005g0224 | 3 | HG02132.hp2 NA19002.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1663-81_1663-80ins others(72): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | CCTGCTCC others(157): Show |
1 | a0001c0001t0002g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1663-81_1663-80ins others(164): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290173 | |||||
| chr1:1290173
|
C | T | 108 | a0001c0001t0001g0168a0001c0001t0001g0181a0001c0001t0001g0187others(105): Show | 108 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1663-98C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290173 | ||||||
| chr1:1290178
|
T | C | 2 | a0002c0003t0004g0113a0011c0023t0001g0265 | 2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1663-93T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290178 | ||||||
| chr1:1290178
|
T | TCCGTCCC others(49): Show |
1 | a0028c0038t0003g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1663-86_1663-85ins others(56): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290178 | |||||
| chr1:1290179
|
C | G | 2 | a0012c0022t0006g0132a0012c0022t0006g0269 | 2 | HG00642.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1663-92C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290179 | ||||||
| chr1:1290180
|
C | T | 2 | a0012c0022t0006g0132a0012c0022t0006g0269 | 2 | HG00642.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1663-91C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290180 | ||||||
| chr1:1290181
|
G | GTCCCGTG others(885): Show |
1 | a0005c0017t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1663-58_1663-57ins others(892): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290181 | |||||
| chr1:1290182
|
T | TCC | 4 | a0002c0002t0001g0102a0003c0004t0003g0138a0004c0005t0010g0125others(1): Show | 4 | HG01496.hp1 NA18522.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-87_1663-86dup others(2): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290182 | |||||
| chr1:1290182
|
T | TCCCGTGT others(2089): Show |
1 | a0001c0001t0001g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1663-81_1663-80ins others(2096): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290182 | |||||
| chr1:1290186
|
G | A | 1 | a0002c0003t0002g0015 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1663-85G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290186 | ||||||
| chr1:1290191
|
C | CCTGCTCC others(11): Show |
1 | a0005c0017t0002g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1663-75_1663-58dup others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290191 | |||||
| chr1:1290191
|
C | T | 49 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0001g0194others(46): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1663-80C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290191 | ||||||
| chr1:1290196
|
T | C | 40 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0001g0194others(37): Show | 40 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1663-75T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290196 | ||||||
| chr1:1290196
|
T | TCCGTCCC others(865): Show |
1 | a0029c0025t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1663-68_1663-67ins others(872): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290196 | |||||
| chr1:1290196
|
T | TCCGTCCC others(11): Show |
1 | a0003c0004t0003g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1663-63_1663-62ins others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290196 | |||||
| chr1:1290199
|
G | A | 5 | a0001c0001t0002g0254a0005c0011t0001g0156a0005c0011t0001g0157others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-72G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290199 | ||||||
| chr1:1290199
|
G | C | 84 | a0001c0001t0002g0161a0001c0001t0002g0163a0001c0001t0002g0229others(81): Show | 84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1663-72G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290199 | ||||||
| chr1:1290199
|
G | GTCCCGTG others(11): Show |
1 | a0001c0001t0002g0225 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1663-58_1663-57ins others(18): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290199 | |||||
| chr1:1290200
|
T | TCCCGTGT others(103): Show |
1 | a0002c0003t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1663-50_1663-49ins others(110): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290200 | |||||
| chr1:1290200
|
T | TCCCGTGT others(85): Show |
2 | a0002c0003t0004g0113a0002c0003t0004g0115 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1663-50_1663-49ins others(92): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290200 | |||||
| chr1:1290209
|
T | C | 2 | a0011c0023t0001g0265a0027c0039t0002g0136 | 2 | HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1663-62T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290209 | ||||||
| chr1:1290214
|
C | T | 2 | a0002c0002t0001g0102a0027c0039t0002g0136 | 2 | HG03942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1663-57C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290214 | ||||||
| chr1:1290217
|
G | A | 4 | a0002c0002t0001g0056a0002c0003t0002g0038a0002c0003t0002g0064others(1): Show | 4 | HG03239.hp1 NA18971.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-54G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290217 | ||||||
| chr1:1290220
|
C | CCCCGTGT others(125): Show |
1 | a0002c0003t0002g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1663-48_1663-47ins others(132): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290220 | |||||
| chr1:1290224
|
A | G | 2 | a0002c0002t0001g0096a0002c0003t0002g0105 | 2 | HG03017.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1663-47A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290224 | ||||||
| chr1:1290232
|
G | A | 72 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0187others(69): Show | 72 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1663-39G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290232 | ||||||
| chr1:1290232
|
G | GCTCCATC others(399): Show |
1 | a0001c0009t0001g0210 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1663-30_1663-29ins others(406): Show |
SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 1290232 | |||||
| chr1:1290261
|
C | A | 177 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0194others(174): Show | 177 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1663-10C>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 12/17 | chr1 | 1290261 | ||||||
| chr1:1290401
|
C | T | 1 | a0003c0004t0003g0151 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1780+13C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 13/17 | chr1 | 1290401 | ||||||
| chr1:1290424
|
A | G | 2 | a0002c0003t0004g0113a0002c0003t0004g0120 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1780+36A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 13/17 | chr1 | 1290424 | ||||||
| chr1:1290444
|
G | A | 5 | a0005c0017t0001g0282a0008c0007t0004g0284a0008c0007t0004g0285others(2): Show | 5 | HG01123.hp2 HG02109.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1781-33G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 13/17 | chr1 | 1290444 | ||||||
| chr1:1290565
|
G | C | 9 | a0005c0017t0001g0282a0008c0007t0004g0284a0008c0007t0004g0285others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1859+10G>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 14/17 | chr1 | 1290565 | ||||||
| chr1:1290579
|
C | G | 187 | a0001c0001t0001g0162a0001c0001t0001g0207a0001c0001t0001g0212others(184): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1859+24C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 14/17 | chr1 | 1290579 | ||||||
| chr1:1290722
|
G | A | 93 | a0001c0001t0001g0209a0001c0001t0001g0223a0001c0001t0002g0221others(90): Show | 93 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1917+28G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290722 | ||||||
| chr1:1290753
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1917+59C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290753 | ||||||
| chr1:1290784
|
G | A | 3 | a0005c0011t0001g0156a0005c0011t0001g0157a0005c0011t0001g0158 | 3 | HG02622.hp2 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1917+90G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290784 | ||||||
| chr1:1290821
|
C | T | 4 | a0001c0036t0006g0123a0004c0005t0006g0128a0004c0005t0010g0124others(1): Show | 4 | HG02895.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1918-74C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290821 | ||||||
| chr1:1290841
|
A | G | 185 | a0001c0001t0001g0162a0001c0001t0001g0195a0001c0001t0001g0207others(182): Show | 185 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1918-54A>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290841 | ||||||
| chr1:1290851
|
G | A | 17 | a0001c0001t0002g0260a0003c0004t0003g0004a0003c0004t0003g0005others(14): Show | 17 | HG01346.hp1 HG02132.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.1918-44G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290851 | ||||||
| chr1:1290853
|
G | A | 7 | a0008c0007t0004g0266a0008c0007t0004g0284a0008c0007t0004g0285others(4): Show | 7 | HG00642.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1918-42G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290853 | ||||||
| chr1:1290867
|
G | A | 3 | a0002c0002t0001g0031a0002c0002t0001g0095a0002c0028t0001g0093 | 3 | HG00621.hp2 HG00673.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1918-28G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290867 | ||||||
| chr1:1290887
|
G | A | 13 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0243others(10): Show | 13 | HG01109.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1918-8G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 15/17 | chr1 | 1290887 | ||||||
| chr1:1290968
|
C | G | 165 | a0001c0001t0001g0195a0001c0001t0001g0209a0001c0001t0001g0223others(162): Show | 165 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1976+15C>G | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 16/17 | chr1 | 1290968 | ||||||
| chr1:1290970
|
C | T | 8 | a0008c0007t0004g0266a0008c0007t0004g0284a0008c0007t0004g0285others(5): Show | 8 | HG00642.hp1 HG02109.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1976+17C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 16/17 | chr1 | 1290970 | ||||||
| chr1:1291043
|
T | C | 6 | a0001c0001t0001g0162a0001c0001t0001g0195a0001c0009t0001g0205others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1977-22T>C | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 16/17 | chr1 | 1291043 | ||||||
| chr1:1291061
|
C | T | 1 | a0002c0003t0001g0091 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.1977-4C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 16/17 | chr1 | 1291061 | ||||||
| chr1:1291159
|
C | T | 1 | a0001c0047t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2052+19C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/17 | chr1 | 1291159 | ||||||
| chr1:1291225
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2053-29C>T | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/17 | chr1 | 1291225 | ||||||
| chr1:1291250
|
G | A | 1 | a0002c0003t0001g0060 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.2053-4G>A | SCNN1D | ENSG00000162572.21 | transcript | ENST00000379116.10 | protein_coding | 17/17 | chr1 | 1291250 |