geneid | 6338 |
---|---|
ensemblid | ENSG00000168447.11 |
hgncid | 10600 |
symbol | SCNN1B |
name | sodium channel epithelial 1 subunit beta |
refseq_nuc | NM_000336.3 |
refseq_prot | NP_000327.2 |
ensembl_nuc | ENST00000343070.7 |
ensembl_prot | ENSP00000345751.2 |
mane_status | MANE Select |
chr | chr16 |
start | 23302302 |
end | 23381294 |
strand | + |
ver | v1.2 |
region | chr16:23302302-23381294 |
region5000 | chr16:23297302-23386294 |
regionname0 | SCNN1B_chr16_23302302_23381294 |
regionname5000 | SCNN1B_chr16_23297302_23386294 |
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 | 640 | 289 | 72 | 54 | 107 | 16 | 38 | 82 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0002 | 0/0 | 640 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0003 | 0/0 | 640 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0004 | 0/0 | 640 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0005 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0006 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0007 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
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 | 0/0 | 1923 | 215 | 47 | 31 | 101 | 8 | 28 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0002 | 1/1 | 1923 | 40 | 2 | 20 | 2 | 4 | 10 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0003 | 0/0 | 1923 | 22 | 17 | 2 | 0 | 3 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0004 | 0/0 | 1923 | 6 | 5 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0005 | 0/0 | 1923 | 4 | 4 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0006 | 0/0 | 1923 | 3 | 0 | 0 | 3 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0007 | 0/0 | 1923 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0008 | 0/0 | 1923 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0009 | 0/0 | 1923 | 2 | 1 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0010 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0012 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0013 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0014 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0015 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0016 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
c0017 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
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 | 638 | 299 | 81 | 55 | 108 | 16 | 37 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
t0002 | 0/0 | 638 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
t0003 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
t0004 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
t0005 | 0/0 | 638 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
t0006 | 0/0 | 638 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
t0007 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0246 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0256 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
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 | 0/0 | 1923 | 215 | 47 | 31 | 101 | 8 | 28 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0002 | 1/1 | 1923 | 40 | 2 | 20 | 2 | 4 | 10 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0003 | 0/0 | 1923 | 22 | 17 | 2 | 0 | 3 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0006 | 0/0 | 1923 | 3 | 0 | 0 | 3 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0008 | 0/0 | 1923 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0009 | 0/0 | 1923 | 2 | 1 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0012 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0013 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0015 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0002c0004 | 0/0 | 1923 | 6 | 5 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0002c0007 | 0/0 | 1923 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0003c0005 | 0/0 | 1923 | 4 | 4 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0004c0017 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0005c0016 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0006c0014 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0007c0010 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2560 | 210 | 43 | 31 | 101 | 8 | 27 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0001t0002 | 0/0 | 2560 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0001t0004 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0001t0006 | 0/0 | 2560 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0001t0007 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0002t0001 | 1/1 | 2560 | 39 | 2 | 19 | 2 | 4 | 10 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0002t0005 | 0/0 | 2560 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0003t0001 | 0/0 | 2560 | 22 | 17 | 2 | 0 | 3 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0006t0001 | 0/0 | 2560 | 3 | 0 | 0 | 3 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0008t0001 | 0/0 | 2560 | 2 | 2 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0008t0003 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0009t0001 | 0/0 | 2560 | 2 | 1 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0011t0001 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0012t0001 | 0/0 | 2560 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0013t0001 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0001c0015t0001 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0002c0004t0001 | 0/0 | 2560 | 6 | 5 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0002c0007t0001 | 0/0 | 2560 | 3 | 3 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0003c0005t0001 | 0/0 | 2560 | 4 | 4 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0004c0017t0001 | 0/0 | 2560 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0005c0016t0001 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0006c0014t0001 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
a0007c0010t0001 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | copy fasta | chr16 | 23297302 | 23386294 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0246 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0256 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0008t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0008t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0009t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0011t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0012t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0013t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0001c0015t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0007t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0007t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0002c0007t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0003c0005t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0003c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0003c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0003c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0004c0017t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0005c0016t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0006c0014t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
a0007c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | GBR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0198 | EUR | GBR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0048 | EUR | FIN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00639 | hp2 | a0002 | c0004 | t0001 | g0040 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01081 | hp2 | a0001 | c0012 | t0001 | g0196 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01243 | hp1 | a0001 | c0002 | t0005 | g0233 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01255 | hp1 | a0004 | c0017 | t0001 | g0015 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0200 | EUR | IBS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01516 | hp2 | a0001 | c0009 | t0001 | g0191 | EUR | IBS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | IBS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0249 | EUR | IBS | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01891 | hp2 | a0002 | c0007 | t0001 | g0294 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02027 | hp2 | a0007 | c0010 | t0001 | g0127 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02055 | hp2 | a0002 | c0007 | t0001 | g0283 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02135 | hp1 | a0001 | c0006 | t0001 | g0027 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02258 | hp2 | a0001 | c0011 | t0001 | g0013 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02280 | hp1 | a0002 | c0004 | t0001 | g0005 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02615 | hp1 | a0001 | c0009 | t0001 | g0059 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02622 | hp2 | a0002 | c0004 | t0001 | g0051 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02630 | hp1 | a0001 | c0008 | t0001 | g0148 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02723 | hp2 | a0006 | c0014 | t0001 | g0081 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0287 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02896 | hp2 | a0002 | c0004 | t0001 | g0082 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0289 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02965 | hp2 | a0001 | c0015 | t0001 | g0073 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02976 | hp1 | a0003 | c0005 | t0001 | g0066 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0288 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03139 | hp1 | a0002 | c0007 | t0001 | g0087 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03195 | hp2 | a0003 | c0005 | t0001 | g0065 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0090 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03486 | hp1 | a0003 | c0005 | t0001 | g0004 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0302 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03579 | hp1 | a0002 | c0004 | t0001 | g0151 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0185 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0184 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0199 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0305 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | YRI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18906 | hp2 | a0001 | c0008 | t0001 | g0291 | AFR | YRI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18991 | hp1 | a0001 | c0006 | t0001 | g0247 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19003 | hp2 | a0001 | c0013 | t0001 | g0067 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19043 | hp2 | a0003 | c0005 | t0001 | g0075 | AFR | LWK | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19070 | hp2 | a0001 | c0006 | t0001 | g0025 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ASW | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0103 | EUR | TSI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0039 | EUR | TSI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | GIH | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | GIH | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02109 | hp1 | a0005 | c0016 | t0001 | g0076 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02486 | hp1 | a0001 | c0008 | t0003 | g0091 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02559 | hp1 | a0002 | c0004 | t0001 | g0058 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0274 | AFR | ACB | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0292 | AFR | USA | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | USA | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | USA | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | USA | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0246 | REF | REF | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0256 | REF | REF | SCNN1B_chr16_23297302_23386294 | SCNN1B | chr16 | 23297302 | 23386294 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:23375747
|
C | T | 1 | a0003 | 4 | HG02976.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.1162C>T | p.Arg388Cys | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/13 | 1306/2560 | 1162/1923 | 388/640 | chr16 | 23375747 | ||
chr16:23375748
|
G | A | 1 | a0004 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1163G>A | p.Arg388His | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/13 | 1307/2560 | 1163/1923 | 388/640 | chr16 | 23375748 | ||
chr16:23375775
|
G | T | 1 | a0005 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1190G>T | p.Arg397Leu | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/13 | 1334/2560 | 1190/1923 | 397/640 | chr16 | 23375775 | ||
chr16:23377219
|
G | T | 2 | a0002a0003 | 13 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
missense_variant | MODERATE | c.1325G>T | p.Gly442Val | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 9/13 | 1469/2560 | 1325/1923 | 442/640 | chr16 | 23377219 | ||
chr16:23380659
|
C | T | 1 | a0006 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1781C>T | p.Thr594Met | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 1925/2560 | 1781/1923 | 594/640 | chr16 | 23380659 | ||
chr16:23380793
|
G | A | 1 | a0007 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.1915G>A | p.Ala639Thr | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 2059/2560 | 1915/1923 | 639/640 | chr16 | 23380793 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:23348878
|
T | C | 14 | a0001c0001a0001c0003a0001c0006others(11): Show | 263 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(260): Show |
synonymous_variant | LOW | c.279T>C | p.Pro93Pro | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/13 | 423/2560 | 279/1923 | 93/640 | chr16 | 23348878 | ||
chr16:23348881
|
C | T | 1 | a0001c0008 | 3 | HG02486.hp1 HG02630.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.282C>T | p.Ala94Ala | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/13 | 426/2560 | 282/1923 | 94/640 | chr16 | 23348881 | ||
chr16:23367958
|
C | T | 7 | a0001c0003a0001c0008a0001c0009others(4): Show | 33 | HG01074.hp1 HG01167.hp2 HG01516.hp1 others(30): Show |
splice_region_variant&synonymous_variant | LOW | c.879C>T | p.Phe293Phe | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/13 | 1023/2560 | 879/1923 | 293/640 | chr16 | 23367958 | ||
chr16:23371423
|
C | T | 1 | a0001c0013 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1005C>T | p.Tyr335Tyr | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/13 | 1149/2560 | 1005/1923 | 335/640 | chr16 | 23371423 | ||
chr16:23375806
|
A | G | 1 | a0001c0012 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.1221A>G | p.Pro407Pro | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/13 | 1365/2560 | 1221/1923 | 407/640 | chr16 | 23375806 | ||
chr16:23375842
|
C | T | 1 | a0001c0006 | 3 | HG02135.hp1 NA18991.hp1 NA19070.hp2 |
synonymous_variant | LOW | c.1257C>T | p.Asp419Asp | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/13 | 1401/2560 | 1257/1923 | 419/640 | chr16 | 23375842 | ||
chr16:23377383
|
C | T | 1 | a0001c0011 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1401C>T | p.Ser467Ser | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/13 | 1545/2560 | 1401/1923 | 467/640 | chr16 | 23377383 | ||
chr16:23380609
|
C | T | 1 | a0001c0015 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1731C>T | p.Thr577Thr | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 1875/2560 | 1731/1923 | 577/640 | chr16 | 23380609 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:23380868
|
A | G | 1 | a0001c0001t0007 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*67A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 67 | chr16 | 23380868 | |||||
chr16:23380962
|
A | G | 1 | a0001c0001t0006 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 161 | chr16 | 23380962 | |||||
chr16:23381079
|
C | T | 1 | a0001c0002t0005 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 278 | chr16 | 23381079 | |||||
chr16:23381105
|
C | A | 1 | a0001c0008t0003 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 304 | chr16 | 23381105 | |||||
chr16:23381152
|
C | T | 1 | a0001c0001t0002 | 2 | HG02809.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*351C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 351 | chr16 | 23381152 | |||||
chr16:23381201
|
G | A | 1 | a0001c0001t0004 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 13/13 | 400 | chr16 | 23381201 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:23302558
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG01884.hp1 HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-9+121G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23302558 | ||||||
chr16:23302561
|
A | T | 7 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0303others(4): Show | 7 | HG03239.hp2 HG03492.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+124A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23302561 | ||||||
chr16:23302675
|
C | G | 22 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(19): Show | 22 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9+238C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23302675 | ||||||
chr16:23302732
|
T | C | 106 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-9+295T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23302732 | ||||||
chr16:23302899
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9+462T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23302899 | ||||||
chr16:23302926
|
A | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0004g0086others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+489A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23302926 | ||||||
chr16:23303001
|
G | T | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+564G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303001 | ||||||
chr16:23303232
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-9+795G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303232 | ||||||
chr16:23303391
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-9+954C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303391 | ||||||
chr16:23303530
|
A | C | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(67): Show | 70 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-9+1093A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303530 | ||||||
chr16:23303681
|
T | C | 1 | a0001c0003t0001g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-9+1244T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303681 | ||||||
chr16:23303690
|
C | T | 22 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(19): Show | 22 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9+1253C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303690 | ||||||
chr16:23303733
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-9+1296T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303733 | ||||||
chr16:23303752
|
C | CA | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(17): Show | 20 | HG00735.hp2 HG00741.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+1332dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23303752 | |||||
chr16:23303752
|
CA | C | 36 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(33): Show | 36 | HG01109.hp1 HG01167.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+1332delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23303752 | |||||
chr16:23303788
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+1351A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23303788 | ||||||
chr16:23304053
|
G | A | 2 | a0001c0001t0001g0012a0001c0011t0001g0013 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+1616G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304053 | ||||||
chr16:23304056
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00408.hp1 HG03669.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-9+1619G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304056 | ||||||
chr16:23304072
|
G | A | 1 | a0002c0004t0001g0082 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9+1635G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304072 | ||||||
chr16:23304256
|
C | CACACACA others(5): Show |
22 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(19): Show | 22 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9+1828_-9+1829ins others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23304256 | |||||
chr16:23304256
|
C | CACACACA others(3): Show |
65 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-9+1820_-9+1829dup others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23304256 | |||||
chr16:23304331
|
TACAC | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-9+1898_-9+1901del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23304331 | |||||
chr16:23304454
|
G | A | 9 | a0001c0003t0001g0074a0001c0003t0001g0077a0001c0003t0001g0078others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+2017G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304454 | ||||||
chr16:23304517
|
G | A | 21 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+2080G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304517 | ||||||
chr16:23304572
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-9+2135A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304572 | ||||||
chr16:23304590
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 87 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-9+2153C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304590 | ||||||
chr16:23304730
|
C | T | 10 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(7): Show | 10 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9+2293C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304730 | ||||||
chr16:23304927
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-9+2490C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304927 | ||||||
chr16:23304964
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-9+2527C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23304964 | ||||||
chr16:23305003
|
C | T | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+2566C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305003 | ||||||
chr16:23305088
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-9+2651G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305088 | ||||||
chr16:23305298
|
A | C | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+2861A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305298 | ||||||
chr16:23305369
|
A | C | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+2932A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305369 | ||||||
chr16:23305382
|
G | A | 3 | a0001c0001t0001g0084a0001c0003t0001g0083a0002c0004t0001g0082 | 3 | HG02572.hp1 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-9+2945G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305382 | ||||||
chr16:23305450
|
C | T | 6 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | HG00741.hp2 HG01123.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+3013C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305450 | ||||||
chr16:23305523
|
AAATATAT others(9): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-9+3088_-9+3103del others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305523 | |||||
chr16:23305524
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0258 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-9+3087_-9+3088ins others(15): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305524 | ||||||
chr16:23305524
|
AATATATA others(4): Show |
A | 34 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0062others(31): Show | 34 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3108del others(11): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(6): Show |
A | 22 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0054others(19): Show | 22 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3110del others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(8): Show |
A | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(8): Show | 11 | HG00323.hp1 HG00558.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3112del others(15): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(10): Show |
A | 30 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 30 | HG00099.hp1 HG00639.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3114del others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(16): Show |
A | 1 | a0001c0001t0001g0306 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+3098_-9+3120del others(23): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(18): Show |
A | 1 | a0001c0003t0001g0249 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-9+3098_-9+3122del others(25): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(20): Show |
A | 1 | a0001c0001t0001g0250 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-9+3098_-9+3124del others(27): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305524
|
AATATATA others(49): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9+3098_-9+3153del others(56): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305524 | |||||
chr16:23305525
|
ATATATAT others(2): Show |
A | 11 | a0001c0001t0001g0010a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG00323.hp2 HG00544.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3106del others(9): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305525 | |||||
chr16:23305527
|
ATATATAT | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0140a0001c0001t0001g0141others(19): Show | 22 | HG00140.hp1 HG00438.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3104del others(7): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305527 | |||||
chr16:23305529
|
ATATAT | A | 35 | a0001c0001t0001g0070a0001c0001t0001g0146a0001c0001t0001g0147others(32): Show | 35 | HG01167.hp2 HG01358.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3102del others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305529 | |||||
chr16:23305531
|
ATAT | A | 35 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0107others(32): Show | 35 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9+3098_-9+3100del others(3): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305531 | |||||
chr16:23305533
|
AT | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0072others(46): Show | 49 | HG00099.hp2 HG00438.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.-9+3098delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305533 | |||||
chr16:23305534
|
T | TA | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0105others(27): Show | 30 | HG00408.hp1 HG00558.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9+3097_-9+3098ins others(1): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305534 | ||||||
chr16:23305534
|
T | TATA | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0173others(3): Show | 6 | HG01496.hp1 HG02300.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3097_-9+3098ins others(3): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305534 | ||||||
chr16:23305534
|
T | TATATA | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0275others(1): Show | 4 | HG03704.hp2 HG04228.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3097_-9+3098ins others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305534 | ||||||
chr16:23305534
|
T | TATATATA others(4): Show |
2 | a0001c0001t0001g0099a0002c0004t0001g0082 | 2 | HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-9+3097_-9+3098ins others(11): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305534 | ||||||
chr16:23305534
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-9+3097_-9+3098ins others(31): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305534 | ||||||
chr16:23305534
|
TTATATAT others(35): Show |
T | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+3099_-9+3140del others(42): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305534 | |||||
chr16:23305549
|
T | A | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3112T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305549 | ||||||
chr16:23305551
|
T | A | 25 | a0001c0001t0001g0085a0001c0001t0001g0279a0001c0001t0001g0280others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+3114T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305551 | ||||||
chr16:23305553
|
T | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0085others(6): Show | 9 | HG01255.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3116T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305553 | ||||||
chr16:23305555
|
T | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0014a0002c0007t0001g0087others(1): Show | 4 | HG01255.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3118T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305555 | ||||||
chr16:23305555
|
TA | T | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3119delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305555 | ||||||
chr16:23305557
|
TATATATA others(17): Show |
T | 7 | a0001c0001t0001g0085a0001c0001t0001g0248a0001c0001t0004g0086others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3121_-9+3144del others(24): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305557 | ||||||
chr16:23305559
|
TATATATA others(15): Show |
T | 4 | a0001c0001t0001g0006a0001c0001t0001g0014a0002c0007t0001g0087others(1): Show | 4 | HG01255.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3123_-9+3144del others(22): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305559 | ||||||
chr16:23305569
|
T | A | 1 | a0001c0008t0003g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+3132T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305569 | ||||||
chr16:23305571
|
T | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(97): Show | 100 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.-9+3134T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305571 | ||||||
chr16:23305573
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 165 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.-9+3136T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305573 | ||||||
chr16:23305575
|
T | TA | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0162others(1): Show | 4 | HG00408.hp1 HG03471.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+3139dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305575 | |||||
chr16:23305576
|
A | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0231a0001c0001t0001g0261 | 3 | HG00408.hp2 HG02698.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+3139A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305576 | ||||||
chr16:23305577
|
T | A | 10 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0106others(7): Show | 10 | HG00408.hp1 HG00408.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+3140T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305577 | ||||||
chr16:23305577
|
T | TA | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0084others(6): Show | 9 | HG01123.hp2 HG02004.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3140_-9+3141ins others(1): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305577 | ||||||
chr16:23305577
|
TTA | T | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3161_-9+3162del others(2): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305577 | |||||
chr16:23305577
|
TTATA | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 147 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+3159_-9+3162del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305577 | |||||
chr16:23305578
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9+3141T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305578 | ||||||
chr16:23305580
|
TA | T | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0162others(2): Show | 5 | HG00408.hp1 HG02559.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3144delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305580 | ||||||
chr16:23305581
|
A | AAATAT | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0099others(2): Show | 5 | HG01123.hp2 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3144_-9+3145ins others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305581 | ||||||
chr16:23305581
|
A | AT | 4 | a0001c0001t0001g0084a0001c0001t0001g0163a0001c0003t0001g0083others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+3145dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23305581 | |||||
chr16:23305583
|
A | T | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+3146A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305583 | ||||||
chr16:23305625
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-9+3188C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23305625 | ||||||
chr16:23306058
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-9+3621C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306058 | ||||||
chr16:23306105
|
T | C | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3668T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306105 | ||||||
chr16:23306182
|
G | A | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3745G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306182 | ||||||
chr16:23306192
|
G | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3755G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306192 | ||||||
chr16:23306241
|
C | CA | 6 | a0001c0001t0001g0016a0001c0001t0001g0092a0001c0001t0001g0117others(3): Show | 6 | HG02027.hp1 HG02071.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3819dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23306241 | |||||
chr16:23306241
|
CA | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+3819delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23306241 | |||||
chr16:23306243
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-9+3806A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306243 | ||||||
chr16:23306276
|
G | T | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+3839G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306276 | ||||||
chr16:23306545
|
A | AG | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.-9+4109dupG | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23306545 | |||||
chr16:23306883
|
C | G | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+4446C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306883 | ||||||
chr16:23306885
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-9+4448C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306885 | ||||||
chr16:23306901
|
A | G | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+4464A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306901 | ||||||
chr16:23306993
|
G | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+4556G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23306993 | ||||||
chr16:23307295
|
C | CT | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.-9+4878dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23307295 | |||||
chr16:23307295
|
C | CTT | 79 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(76): Show | 79 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9+4877_-9+4878dup others(2): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23307295 | |||||
chr16:23307545
|
C | T | 3 | a0001c0001t0001g0084a0001c0003t0001g0083a0002c0004t0001g0082 | 3 | HG02572.hp1 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-9+5108C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307545 | ||||||
chr16:23307556
|
G | A | 16 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0092others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9+5119G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307556 | ||||||
chr16:23307565
|
C | G | 72 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(69): Show | 72 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-9+5128C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307565 | ||||||
chr16:23307600
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 116 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-9+5163A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307600 | ||||||
chr16:23307695
|
T | C | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+5258T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307695 | ||||||
chr16:23307788
|
G | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+5351G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307788 | ||||||
chr16:23307862
|
C | A | 20 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+5425C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307862 | ||||||
chr16:23307885
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9+5448A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307885 | ||||||
chr16:23307976
|
T | C | 8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+5539T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23307976 | ||||||
chr16:23308296
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-9+5859G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308296 | ||||||
chr16:23308305
|
T | C | 1 | a0001c0002t0001g0169 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-9+5868T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308305 | ||||||
chr16:23308358
|
G | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+5921G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308358 | ||||||
chr16:23308604
|
ATTTAT | A | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+6180_-9+6184del others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23308604 | |||||
chr16:23308808
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9+6371T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308808 | ||||||
chr16:23308835
|
G | A | 4 | a0001c0003t0001g0139a0001c0008t0001g0148a0002c0004t0001g0005others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6398G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308835 | ||||||
chr16:23308855
|
G | A | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+6418G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308855 | ||||||
chr16:23308866
|
G | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0137others(5): Show | 8 | HG01168.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+6429G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308866 | ||||||
chr16:23308946
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-9+6509A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308946 | ||||||
chr16:23308991
|
A | T | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+6554A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23308991 | ||||||
chr16:23309004
|
G | A | 1 | a0001c0003t0001g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+6567G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309004 | ||||||
chr16:23309135
|
A | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-9+6698A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309135 | ||||||
chr16:23309191
|
A | T | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+6754A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309191 | ||||||
chr16:23309318
|
C | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-9+6881C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309318 | ||||||
chr16:23309410
|
T | TGATA | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0108others(63): Show | 66 | HG00438.hp1 HG01106.hp2 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.-9+7000_-9+7003dup others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23309410 | |||||
chr16:23309410
|
T | TGATAGAT others(1): Show |
19 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0099others(16): Show | 19 | HG01074.hp1 HG01109.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.-9+6996_-9+7003dup others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23309410 | |||||
chr16:23309410
|
T | TGATAGAT others(5): Show |
6 | a0001c0001t0001g0070a0001c0001t0001g0156a0001c0001t0001g0298others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+6992_-9+7003dup others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23309410 | |||||
chr16:23309410
|
TGATA | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(79): Show | 82 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-9+7000_-9+7003del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23309410 | |||||
chr16:23309410
|
TGATAGAT others(5): Show |
T | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+6992_-9+7003del others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23309410 | |||||
chr16:23309437
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9+7000T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309437 | ||||||
chr16:23309441
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9+7004C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309441 | ||||||
chr16:23309459
|
G | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-9+7022G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309459 | ||||||
chr16:23309471
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-9+7034A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309471 | ||||||
chr16:23309595
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+7158G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309595 | ||||||
chr16:23309674
|
G | T | 7 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(4): Show | 7 | HG01934.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+7237G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23309674 | ||||||
chr16:23309755
|
TC | T | 3 | a0001c0001t0001g0085a0001c0001t0004g0086a0002c0007t0001g0087 | 3 | HG02145.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-9+7320delC | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23309755 | |||||
chr16:23310017
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+7580A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23310017 | ||||||
chr16:23310129
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-9+7692C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23310129 | ||||||
chr16:23310290
|
C | CA | 44 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0098others(41): Show | 44 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+7876dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23310290 | |||||
chr16:23310290
|
CA | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(16): Show | 19 | HG01109.hp1 HG01123.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9+7876delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23310290 | |||||
chr16:23310290
|
CAAAAAAA others(2): Show |
C | 51 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(48): Show | 51 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.-9+7868_-9+7876del others(9): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23310290 | |||||
chr16:23310290
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-9+7867_-9+7876del others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23310290 | |||||
chr16:23310313
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-9+7876A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23310313 | ||||||
chr16:23310635
|
C | T | 30 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0119others(27): Show | 30 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9+8198C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23310635 | ||||||
chr16:23310824
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8387G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23310824 | ||||||
chr16:23310916
|
C | T | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8479C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23310916 | ||||||
chr16:23311064
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8627G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311064 | ||||||
chr16:23311078
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+8641G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311078 | ||||||
chr16:23311124
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8687G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311124 | ||||||
chr16:23311135
|
C | T | 2 | a0001c0003t0001g0139a0001c0008t0001g0148 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+8698C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311135 | ||||||
chr16:23311270
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-9+8833C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311270 | ||||||
chr16:23311286
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8849G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311286 | ||||||
chr16:23311312
|
A | G | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8875A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311312 | ||||||
chr16:23311388
|
T | C | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+8951T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311388 | ||||||
chr16:23311392
|
A | T | 1 | a0001c0003t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-9+8955A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311392 | ||||||
chr16:23311418
|
C | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0003t0001g0113 | 3 | HG02451.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+8981C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311418 | ||||||
chr16:23311596
|
G | A | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+9159G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311596 | ||||||
chr16:23311602
|
C | A | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+9165C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311602 | ||||||
chr16:23311683
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+9246G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311683 | ||||||
chr16:23311683
|
G | C | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+9246G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311683 | ||||||
chr16:23311728
|
A | AG | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(76): Show | 79 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.-9+9292dupG | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23311728 | |||||
chr16:23311816
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+9379G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311816 | ||||||
chr16:23311816
|
G | C | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+9379G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311816 | ||||||
chr16:23311838
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-9+9401G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311838 | ||||||
chr16:23311951
|
C | T | 2 | a0001c0003t0001g0139a0001c0008t0001g0148 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+9514C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23311951 | ||||||
chr16:23312161
|
G | C | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+9724G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312161 | ||||||
chr16:23312211
|
C | A | 3 | a0001c0001t0001g0084a0001c0003t0001g0083a0002c0004t0001g0082 | 3 | HG02572.hp1 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-9+9774C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312211 | ||||||
chr16:23312244
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0140a0001c0001t0001g0142others(1): Show | 4 | HG00438.hp1 NA18948.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+9807A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312244 | ||||||
chr16:23312262
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0001g0279a0001c0001t0001g0280others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+9825G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312262 | ||||||
chr16:23312418
|
A | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(102): Show | 105 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-9+9981A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312418 | ||||||
chr16:23312453
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(77): Show | 80 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.-9+10016G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312453 | ||||||
chr16:23312552
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-9+10115G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312552 | ||||||
chr16:23312705
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(102): Show | 105 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-9+10268T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312705 | ||||||
chr16:23312810
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-9+10373C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23312810 | ||||||
chr16:23313067
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9+10630G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313067 | ||||||
chr16:23313082
|
G | A | 1 | a0001c0003t0001g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+10645G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313082 | ||||||
chr16:23313115
|
G | GT | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+10679dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23313115 | |||||
chr16:23313244
|
T | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(72): Show | 75 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-9+10807T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313244 | ||||||
chr16:23313528
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(78): Show | 81 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.-9+11091C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313528 | ||||||
chr16:23313586
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(78): Show | 81 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.-9+11149T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313586 | ||||||
chr16:23313690
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0041 | 3 | NA18957.hp1 NA18979.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-9+11253C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313690 | ||||||
chr16:23313758
|
C | T | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+11321C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23313758 | ||||||
chr16:23314003
|
T | C | 12 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+11566T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314003 | ||||||
chr16:23314333
|
C | T | 33 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(30): Show | 33 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9+11896C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314333 | ||||||
chr16:23314394
|
T | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+11957T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314394 | ||||||
chr16:23314436
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-9+11999G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314436 | ||||||
chr16:23314486
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9+12049A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314486 | ||||||
chr16:23314641
|
A | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0278 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-9+12204A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314641 | ||||||
chr16:23314690
|
G | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | NA18968.hp2 NA19063.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+12253G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314690 | ||||||
chr16:23314710
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0006t0001g0027 | 3 | HG02135.hp1 NA18954.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-9+12273A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314710 | ||||||
chr16:23314741
|
G | C | 33 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(30): Show | 33 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9+12304G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314741 | ||||||
chr16:23314817
|
G | A | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0099others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+12380G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314817 | ||||||
chr16:23314834
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-9+12397T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314834 | ||||||
chr16:23314878
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG01070.hp1 HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-9+12441G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23314878 | ||||||
chr16:23315026
|
A | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9+12589A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315026 | ||||||
chr16:23315153
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-9+12716A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315153 | ||||||
chr16:23315211
|
C | T | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+12774C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315211 | ||||||
chr16:23315229
|
C | T | 2 | a0001c0001t0001g0021a0001c0006t0001g0025 | 2 | NA19011.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-9+12792C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315229 | ||||||
chr16:23315286
|
A | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(35): Show | 38 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9+12849A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315286 | ||||||
chr16:23315329
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-9+12892G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315329 | ||||||
chr16:23315481
|
G | C | 1 | a0001c0009t0001g0191 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-9+13044G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315481 | ||||||
chr16:23315517
|
A | T | 1 | a0001c0001t0001g0222 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-9+13080A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315517 | ||||||
chr16:23315648
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-9+13211C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315648 | ||||||
chr16:23315752
|
C | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+13315C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23315752 | ||||||
chr16:23315972
|
CCATCCTC others(8): Show |
C | 2 | a0002c0004t0001g0051a0002c0004t0001g0058 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-9+13537_-9+13551d others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23315972 | |||||
chr16:23316028
|
A | ATCACCAT others(8): Show |
185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-9+13603_-9+13604i others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316028 | |||||
chr16:23316134
|
TCAC | T | 3 | a0001c0002t0001g0060a0001c0003t0001g0064a0001c0009t0001g0059 | 3 | HG01891.hp1 HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-9+13703_-9+13705d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316134 | |||||
chr16:23316262
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-9+13825A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23316262 | ||||||
chr16:23316342
|
C | T | 3 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0056 | 3 | HG00099.hp1 HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-9+13905C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23316342 | ||||||
chr16:23316346
|
G | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(97): Show | 100 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-9+13909G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23316346 | ||||||
chr16:23316395
|
T | TCAC | 38 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(35): Show | 38 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9+13960_-9+13961i others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316395 | |||||
chr16:23316430
|
TTCA | T | 3 | a0001c0001t0001g0203a0001c0003t0001g0064a0001c0003t0001g0159 | 3 | HG01074.hp1 HG01106.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-9+14000_-9+14002d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316430 | |||||
chr16:23316571
|
ATCACCAC others(11): Show |
A | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+14152_-9+14169d others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316571 | |||||
chr16:23316578
|
CCATCACC others(20): Show |
C | 8 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+14152_-9+14178d others(29): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316578 | |||||
chr16:23316589
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(64): Show | 67 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-9+14152T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23316589 | ||||||
chr16:23316705
|
CATCACCA others(80): Show |
C | 2 | a0001c0002t0005g0233a0001c0009t0001g0191 | 2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-9+14298_-9+14384d others(89): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23316705 | |||||
chr16:23316739
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0144others(4): Show | 7 | HG00735.hp1 HG01081.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+14302A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23316739 | ||||||
chr16:23316754
|
C | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+14317C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23316754 | ||||||
chr16:23317001
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(95): Show | 98 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9+14564A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317001 | ||||||
chr16:23317246
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-9+14809G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317246 | ||||||
chr16:23317247
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-9+14810C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317247 | ||||||
chr16:23317432
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-9+14995G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317432 | ||||||
chr16:23317550
|
C | T | 15 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+15113C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317550 | ||||||
chr16:23317587
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-9+15150C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317587 | ||||||
chr16:23317589
|
T | G | 1 | a0002c0004t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9+15152T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317589 | ||||||
chr16:23317602
|
C | G | 1 | a0001c0003t0001g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+15165C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317602 | ||||||
chr16:23317751
|
A | G | 33 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(30): Show | 33 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9+15314A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23317751 | ||||||
chr16:23318052
|
G | T | 33 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(30): Show | 33 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9+15615G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318052 | ||||||
chr16:23318076
|
C | T | 8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+15639C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318076 | ||||||
chr16:23318215
|
C | T | 2 | a0001c0002t0001g0201a0001c0002t0001g0219 | 2 | HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-9+15778C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318215 | ||||||
chr16:23318314
|
T | C | 33 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(30): Show | 33 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9+15877T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318314 | ||||||
chr16:23318391
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-9+15954T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318391 | ||||||
chr16:23318421
|
C | T | 8 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+15984C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318421 | ||||||
chr16:23318466
|
G | A | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+16029G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318466 | ||||||
chr16:23318557
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9+16120C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318557 | ||||||
chr16:23318591
|
A | G | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+16154A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318591 | ||||||
chr16:23318637
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-9+16200A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318637 | ||||||
chr16:23318707
|
A | T | 2 | a0002c0004t0001g0051a0002c0004t0001g0058 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-9+16270A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318707 | ||||||
chr16:23318791
|
G | A | 1 | a0002c0004t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+16354G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23318791 | ||||||
chr16:23319026
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-9+16589T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319026 | ||||||
chr16:23319045
|
GT | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(147): Show | 150 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-9+16622delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23319045 | |||||
chr16:23319045
|
GTT | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+16621_-9+16622d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23319045 | |||||
chr16:23319051
|
T | G | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+16614T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319051 | ||||||
chr16:23319068
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0192a0001c0001t0001g0227 | 3 | HG01361.hp1 HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-9+16631G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319068 | ||||||
chr16:23319167
|
C | T | 5 | a0001c0002t0001g0102a0001c0002t0001g0217a0001c0002t0001g0218others(2): Show | 5 | HG00741.hp1 HG01074.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+16730C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319167 | ||||||
chr16:23319184
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9+16747G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319184 | ||||||
chr16:23319255
|
T | C | 8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+16818T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319255 | ||||||
chr16:23319281
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-9+16844C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319281 | ||||||
chr16:23319335
|
T | C | 1 | a0001c0002t0001g0193 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9+16898T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319335 | ||||||
chr16:23319386
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-9+16949G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319386 | ||||||
chr16:23319389
|
A | C | 8 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+16952A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319389 | ||||||
chr16:23319454
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9+17017G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319454 | ||||||
chr16:23319476
|
GA | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0299a0001c0001t0002g0020others(10): Show | 13 | HG00639.hp2 HG01884.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9+17050delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23319476 | |||||
chr16:23319476
|
GAA | G | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+17049_-9+17050d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23319476 | |||||
chr16:23319563
|
G | A | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+17126G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319563 | ||||||
chr16:23319591
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+17154C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319591 | ||||||
chr16:23319626
|
G | A | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+17189G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319626 | ||||||
chr16:23319807
|
G | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+17370G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319807 | ||||||
chr16:23319916
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0131 | 2 | HG02129.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-9+17479C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319916 | ||||||
chr16:23319998
|
C | T | 35 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0111others(32): Show | 35 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9+17561C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319998 | ||||||
chr16:23319999
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9+17562G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23319999 | ||||||
chr16:23320027
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-9+17590G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320027 | ||||||
chr16:23320163
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9+17726G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320163 | ||||||
chr16:23320205
|
G | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+17768G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320205 | ||||||
chr16:23320373
|
C | T | 9 | a0001c0003t0001g0074a0001c0003t0001g0077a0001c0003t0001g0078others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+17936C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320373 | ||||||
chr16:23320392
|
A | G | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+17955A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320392 | ||||||
chr16:23320422
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-9+17985G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320422 | ||||||
chr16:23320605
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9+18168G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320605 | ||||||
chr16:23320709
|
C | T | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+18272C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320709 | ||||||
chr16:23320845
|
C | G | 5 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+18408C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320845 | ||||||
chr16:23320979
|
G | A | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+18542G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23320979 | ||||||
chr16:23321060
|
T | A | 1 | a0001c0001t0001g0017 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-9+18623T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321060 | ||||||
chr16:23321115
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-9+18678G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321115 | ||||||
chr16:23321231
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-9+18794T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321231 | ||||||
chr16:23321261
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-9+18824C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321261 | ||||||
chr16:23321331
|
A | G | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+18894A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321331 | ||||||
chr16:23321333
|
C | T | 1 | a0001c0003t0001g0292 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9+18896C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321333 | ||||||
chr16:23321388
|
G | C | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+18951G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321388 | ||||||
chr16:23321622
|
C | A | 1 | a0001c0002t0001g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9+19185C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321622 | ||||||
chr16:23321753
|
T | C | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+19316T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321753 | ||||||
chr16:23321950
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-9+19513G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23321950 | ||||||
chr16:23322076
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9+19639C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322076 | ||||||
chr16:23322082
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0052others(1): Show | 4 | HG03017.hp1 HG03710.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+19645A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322082 | ||||||
chr16:23322208
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9+19771T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322208 | ||||||
chr16:23322213
|
A | G | 1 | a0001c0003t0001g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+19776A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322213 | ||||||
chr16:23322362
|
A | G | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+19925A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322362 | ||||||
chr16:23322466
|
A | AT | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+20040dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23322466 | |||||
chr16:23322486
|
T | C | 3 | a0001c0001t0001g0084a0001c0003t0001g0083a0002c0004t0001g0082 | 3 | HG02572.hp1 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-9+20049T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322486 | ||||||
chr16:23322599
|
C | G | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+20162C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322599 | ||||||
chr16:23322605
|
C | T | 6 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0303others(3): Show | 6 | HG03239.hp2 HG03834.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+20168C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322605 | ||||||
chr16:23322663
|
C | G | 3 | a0001c0001t0001g0279a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG02451.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+20226C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322663 | ||||||
chr16:23322738
|
G | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+20301G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23322738 | ||||||
chr16:23323030
|
C | CA | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+20607dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23323030 | |||||
chr16:23323051
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-9+20614C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323051 | ||||||
chr16:23323067
|
G | A | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+20630G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323067 | ||||||
chr16:23323097
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9+20660C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323097 | ||||||
chr16:23323159
|
C | G | 8 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+20722C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323159 | ||||||
chr16:23323416
|
T | C | 1 | a0001c0002t0001g0302 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-9+20979T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323416 | ||||||
chr16:23323586
|
A | C | 2 | a0002c0004t0001g0051a0002c0004t0001g0058 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-9+21149A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323586 | ||||||
chr16:23323728
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+21291C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323728 | ||||||
chr16:23323951
|
A | G | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+21514A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23323951 | ||||||
chr16:23324188
|
C | CT | 30 | a0001c0001t0001g0014a0001c0001t0001g0070a0001c0001t0001g0071others(27): Show | 30 | HG01109.hp1 HG01516.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9+21768dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23324188 | |||||
chr16:23324188
|
CT | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0037others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+21768delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23324188 | |||||
chr16:23324340
|
A | C | 8 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+21903A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324340 | ||||||
chr16:23324597
|
T | G | 2 | a0001c0001t0001g0010a0001c0013t0001g0067 | 2 | NA18747.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-9+22160T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324597 | ||||||
chr16:23324745
|
A | G | 35 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0111others(32): Show | 35 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9+22308A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324745 | ||||||
chr16:23324779
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG00741.hp2 HG01123.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+22342G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324779 | ||||||
chr16:23324896
|
C | T | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-9+22459C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324896 | ||||||
chr16:23324917
|
T | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9+22480T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324917 | ||||||
chr16:23324986
|
C | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0278others(1): Show | 4 | HG01074.hp1 HG02109.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+22549C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23324986 | ||||||
chr16:23325044
|
C | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(80): Show | 83 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-9+22607C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325044 | ||||||
chr16:23325230
|
G | C | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+22793G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325230 | ||||||
chr16:23325284
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9+22847G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325284 | ||||||
chr16:23325329
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9+22892C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325329 | ||||||
chr16:23325491
|
C | T | 3 | a0001c0001t0001g0265a0001c0003t0001g0200a0001c0003t0001g0249 | 3 | HG00140.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-9+23054C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325491 | ||||||
chr16:23325533
|
CTGGGATT others(33): Show |
C | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-23056_-8-23017d others(42): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325533 | |||||
chr16:23325646
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(96): Show | 99 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-8-22946A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325646 | ||||||
chr16:23325649
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0276 | 3 | HG03710.hp2 HG04184.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.-8-22943C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325649 | ||||||
chr16:23325887
|
T | TAATA | 16 | a0001c0001t0001g0011a0001c0001t0001g0088a0001c0001t0001g0104others(13): Show | 16 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-22672_-8-22669d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325887 | |||||
chr16:23325920
|
AAT | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-22668_-8-22667d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325920 | |||||
chr16:23325922
|
T | TAA | 4 | a0001c0001t0001g0049a0001c0001t0001g0054a0002c0004t0001g0040others(1): Show | 4 | HG00639.hp2 HG00738.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22669_-8-22668i others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325922 | |||||
chr16:23325922
|
T | TAAATAA | 50 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(47): Show | 50 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.-8-22669_-8-22668i others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325922 | |||||
chr16:23325922
|
T | TAAATAAA others(3): Show |
29 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0035others(26): Show | 29 | HG00408.hp1 HG00735.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-22669_-8-22668i others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325922 | |||||
chr16:23325922
|
T | TAAATAAA others(7): Show |
9 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0050others(6): Show | 9 | HG00558.hp2 HG02071.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-22669_-8-22668i others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325922 | |||||
chr16:23325922
|
T | TAAATAAA others(11): Show |
1 | a0001c0002t0001g0048 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-8-22669_-8-22668i others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23325922 | |||||
chr16:23325924
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-8-22668T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23325924 | ||||||
chr16:23326058
|
G | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0041others(79): Show | 82 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8-22534G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23326058 | ||||||
chr16:23326275
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-8-22317A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23326275 | ||||||
chr16:23326523
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-22069G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23326523 | ||||||
chr16:23326864
|
T | C | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-21728T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23326864 | ||||||
chr16:23326873
|
T | C | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-21719T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23326873 | ||||||
chr16:23327029
|
G | A | 2 | a0002c0004t0001g0051a0002c0004t0001g0058 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-8-21563G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327029 | ||||||
chr16:23327083
|
A | C | 1 | a0002c0004t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-21509A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327083 | ||||||
chr16:23327280
|
C | T | 8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-21312C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327280 | ||||||
chr16:23327362
|
A | G | 8 | a0001c0001t0001g0299a0001c0001t0002g0020a0001c0001t0002g0042others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-21230A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327362 | ||||||
chr16:23327405
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-21187C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327405 | ||||||
chr16:23327421
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0186a0001c0001t0001g0194 | 3 | NA18949.hp2 NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-8-21171T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327421 | ||||||
chr16:23327464
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8-21128G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327464 | ||||||
chr16:23327540
|
GATA | G | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-21035_-8-21033d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23327540 | |||||
chr16:23327556
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8-21036A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327556 | ||||||
chr16:23327617
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8-20975G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327617 | ||||||
chr16:23327647
|
G | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-20945G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327647 | ||||||
chr16:23327715
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-8-20877G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327715 | ||||||
chr16:23327811
|
C | T | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-20781C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327811 | ||||||
chr16:23327835
|
T | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0063 | 3 | HG00558.hp2 HG02056.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-8-20757T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327835 | ||||||
chr16:23327852
|
C | T | 19 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(16): Show | 19 | HG00639.hp2 HG01934.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-20740C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23327852 | ||||||
chr16:23328056
|
C | T | 17 | a0001c0001t0001g0108a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-20536C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328056 | ||||||
chr16:23328130
|
G | T | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-20462G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328130 | ||||||
chr16:23328184
|
A | T | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-20408A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328184 | ||||||
chr16:23328426
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-8-20166C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328426 | ||||||
chr16:23328738
|
G | A | 1 | a0001c0003t0001g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8-19854G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328738 | ||||||
chr16:23328752
|
C | T | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-19840C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328752 | ||||||
chr16:23328766
|
T | C | 3 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0056 | 3 | HG00099.hp1 HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-8-19826T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23328766 | ||||||
chr16:23329092
|
G | A | 1 | a0001c0003t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-19500G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23329092 | ||||||
chr16:23329354
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-19238G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23329354 | ||||||
chr16:23329368
|
G | A | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-19224G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23329368 | ||||||
chr16:23329968
|
G | A | 14 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-18624G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23329968 | ||||||
chr16:23329978
|
G | A | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-8-18614G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23329978 | ||||||
chr16:23330173
|
C | G | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-18419C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330173 | ||||||
chr16:23330274
|
A | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-8-18318A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330274 | ||||||
chr16:23330585
|
G | T | 5 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-18007G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330585 | ||||||
chr16:23330607
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-8-17985C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330607 | ||||||
chr16:23330661
|
C | G | 8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-17931C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330661 | ||||||
chr16:23330720
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-8-17872G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330720 | ||||||
chr16:23330795
|
C | A | 21 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(18): Show | 21 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-17797C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330795 | ||||||
chr16:23330807
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-8-17785C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330807 | ||||||
chr16:23330860
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8-17732C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330860 | ||||||
chr16:23330881
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.-8-17711G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330881 | ||||||
chr16:23330991
|
T | C | 17 | a0001c0001t0001g0108a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-17601T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23330991 | ||||||
chr16:23331111
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-8-17481C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331111 | ||||||
chr16:23331134
|
G | A | 19 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(16): Show | 19 | HG00639.hp2 HG01934.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-17458G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331134 | ||||||
chr16:23331173
|
C | A | 1 | a0001c0002t0001g0169 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-8-17419C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331173 | ||||||
chr16:23331198
|
T | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-17394T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331198 | ||||||
chr16:23331225
|
G | A | 25 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(22): Show | 25 | HG01167.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-17367G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331225 | ||||||
chr16:23331325
|
C | CT | 7 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0267others(4): Show | 7 | HG01099.hp1 HG02630.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-17250dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23331325 | |||||
chr16:23331325
|
C | CTT | 17 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0280others(14): Show | 17 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-17251_-8-17250d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23331325 | |||||
chr16:23331325
|
CT | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-17250delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23331325 | |||||
chr16:23331350
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-8-17242A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331350 | ||||||
chr16:23331516
|
C | T | 1 | a0001c0002t0005g0233 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8-17076C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331516 | ||||||
chr16:23331517
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-8-17075G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331517 | ||||||
chr16:23331550
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8-17042C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331550 | ||||||
chr16:23331784
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8-16808G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331784 | ||||||
chr16:23331946
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8-16646G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23331946 | ||||||
chr16:23332146
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034 | 3 | HG01168.hp1 HG01169.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-8-16446A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332146 | ||||||
chr16:23332194
|
CT | C | 7 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-16386delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23332194 | |||||
chr16:23332227
|
G | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-16365G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332227 | ||||||
chr16:23332289
|
G | C | 2 | a0001c0001t0001g0299a0001c0001t0002g0042 | 2 | HG01934.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-8-16303G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332289 | ||||||
chr16:23332321
|
G | A | 19 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0280others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-16271G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332321 | ||||||
chr16:23332402
|
G | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-16190G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332402 | ||||||
chr16:23332753
|
C | A | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-15839C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332753 | ||||||
chr16:23332838
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-15754G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332838 | ||||||
chr16:23332852
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.-8-15740C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332852 | ||||||
chr16:23332943
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-15649G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332943 | ||||||
chr16:23332985
|
C | T | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-15607C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23332985 | ||||||
chr16:23333012
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0098a0001c0001t0001g0108others(19): Show | 22 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-15580A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333012 | ||||||
chr16:23333043
|
C | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8-15549C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333043 | ||||||
chr16:23333095
|
GAGGA | G | 6 | a0001c0001t0001g0070a0001c0003t0001g0074a0001c0003t0001g0079others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-15485_-8-15482d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(49): Show |
G | 23 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(20): Show | 23 | HG00558.hp2 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-15481_-8-15426d others(58): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(53): Show |
G | 9 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0031others(6): Show | 9 | HG00408.hp1 HG01496.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-15481_-8-15422d others(62): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(57): Show |
G | 16 | a0001c0001t0001g0014a0001c0001t0001g0105a0001c0001t0001g0280others(13): Show | 16 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-15481_-8-15418d others(66): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(61): Show |
G | 2 | a0001c0001t0001g0276a0001c0001t0001g0285 | 2 | HG02280.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-8-15481_-8-15414d others(70): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(65): Show |
G | 1 | a0001c0008t0003g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-15481_-8-15410d others(74): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(69): Show |
G | 4 | a0001c0001t0001g0098a0001c0002t0001g0038a0001c0002t0001g0039others(1): Show | 4 | HG00099.hp1 HG01099.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-15481_-8-15406d others(78): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333095
|
GAGGAAGG others(73): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-8-15481_-8-15402d others(82): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333095 | |||||
chr16:23333097
|
GGAAGGAA others(45): Show |
G | 4 | a0001c0001t0001g0052a0001c0002t0001g0045a0001c0002t0001g0048others(1): Show | 4 | HG00323.hp1 HG03017.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-15481_-8-15430d others(54): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333097 | |||||
chr16:23333101
|
GGAAGGAA others(41): Show |
G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0221others(2): Show | 5 | HG01884.hp2 HG02071.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-15481_-8-15434d others(50): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333101 | |||||
chr16:23333103
|
AAGGAAGG others(1): Show |
A | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0099others(3): Show | 6 | HG01109.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-15485_-8-15478d others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333103 | |||||
chr16:23333107
|
A | AAGGG | 3 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0002t0001g0166 | 3 | HG02572.hp1 HG03704.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-8-15457_-8-15454d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333107 | |||||
chr16:23333107
|
A | G | 2 | a0001c0003t0001g0077a0001c0003t0001g0078 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-15485A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333107 | ||||||
chr16:23333107
|
AAGGG | A | 12 | a0001c0001t0001g0216a0001c0001t0001g0268a0001c0001t0001g0273others(9): Show | 12 | HG01934.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-15457_-8-15454d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333107 | |||||
chr16:23333107
|
AAGGGAGG others(17): Show |
A | 1 | a0001c0001t0001g0041 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-8-15477_-8-15454d others(26): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333107 | |||||
chr16:23333109
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-15483G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333109 | ||||||
chr16:23333117
|
G | C | 50 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-8-15475G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333117 | ||||||
chr16:23333131
|
G | A | 2 | a0001c0003t0001g0077a0001c0003t0001g0078 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8-15461G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333131 | ||||||
chr16:23333133
|
GGGAGGAA others(9): Show |
G | 1 | a0002c0004t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8-15457_-8-15442d others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333133 | |||||
chr16:23333135
|
G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0070others(16): Show | 19 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-15457G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333135 | ||||||
chr16:23333137
|
G | GGGAGGAA others(5): Show |
3 | a0001c0001t0001g0120a0001c0001t0001g0138a0004c0017t0001g0015 | 3 | HG01168.hp2 HG01255.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-8-15454_-8-15453i others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333137 | |||||
chr16:23333139
|
A | G | 22 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0116others(19): Show | 22 | HG00544.hp1 HG00735.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-15453A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333139 | ||||||
chr16:23333141
|
G | A | 1 | a0001c0003t0001g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8-15451G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333141 | ||||||
chr16:23333141
|
G | GGAAA | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0002c0004t0001g0051others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-15448_-8-15447i others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333141 | |||||
chr16:23333145
|
G | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0296a0001c0003t0001g0074others(7): Show | 10 | HG02257.hp1 HG02258.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-15447G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333145 | ||||||
chr16:23333149
|
A | AGAAG | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0023others(38): Show | 41 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-8-15382_-8-15379d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333149
|
A | AGAAGGAA others(1): Show |
19 | a0001c0001t0001g0068a0001c0001t0001g0101a0001c0001t0001g0119others(16): Show | 19 | HG00558.hp1 HG01071.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-15386_-8-15379d others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333149
|
A | AGAAGGAA others(5): Show |
14 | a0001c0001t0001g0124a0001c0001t0001g0161a0001c0001t0001g0186others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-15390_-8-15379d others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333149
|
A | AGAAGGAA others(9): Show |
1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8-15394_-8-15379d others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333149
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0070others(21): Show | 24 | HG01168.hp2 HG01255.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-15443A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333149 | ||||||
chr16:23333149
|
AGAAG | A | 37 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0071others(34): Show | 37 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-8-15382_-8-15379d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333149
|
AGAAGGAA others(1): Show |
A | 31 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0094others(28): Show | 31 | HG00438.hp1 HG00544.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-15386_-8-15379d others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333149
|
AGAAGGAA others(5): Show |
A | 7 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG01243.hp2 HG02129.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-15390_-8-15379d others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333149 | |||||
chr16:23333153
|
G | A | 1 | a0002c0004t0001g0082 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-8-15439G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333153 | ||||||
chr16:23333157
|
G | T | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-8-15435G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333157 | ||||||
chr16:23333161
|
G | A | 2 | a0001c0003t0001g0083a0002c0004t0001g0040 | 2 | HG00639.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-15431G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333161 | ||||||
chr16:23333177
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0029others(2): Show | 5 | HG02165.hp1 NA18959.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-15415G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333177 | ||||||
chr16:23333194
|
GAAGGAAG others(13): Show |
G | 1 | a0003c0005t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-15394_-8-15375d others(22): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333194 | |||||
chr16:23333202
|
GAAGGAAG others(5): Show |
G | 1 | a0002c0004t0001g0005 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-15386_-8-15375d others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333202 | |||||
chr16:23333210
|
G | A | 2 | a0001c0003t0001g0083a0002c0004t0001g0082 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-8-15382G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333210 | ||||||
chr16:23333214
|
A | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-8-15378A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333214 | ||||||
chr16:23333215
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-15377A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333215 | ||||||
chr16:23333247
|
G | A | 51 | a0001c0001t0001g0041a0001c0001t0001g0092a0001c0001t0001g0093others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-15345G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333247 | ||||||
chr16:23333415
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8-15177C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333415 | ||||||
chr16:23333485
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-15107T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333485 | ||||||
chr16:23333551
|
G | C | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8-15041G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333551 | ||||||
chr16:23333626
|
G | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0268a0001c0001t0001g0269others(21): Show | 24 | HG00639.hp2 HG01884.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.-8-14966G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333626 | ||||||
chr16:23333744
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8-14848G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333744 | ||||||
chr16:23333775
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-14817C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333775 | ||||||
chr16:23333813
|
AAAATT | A | 79 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(76): Show | 79 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.-8-14771_-8-14767d others(7): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333813 | |||||
chr16:23333818
|
TAAA | T | 3 | a0001c0001t0001g0001a0001c0003t0001g0139a0001c0008t0001g0148 | 3 | HG01884.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-14773_-8-14771d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333818 | ||||||
chr16:23333862
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-14730C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333862 | ||||||
chr16:23333870
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-8-14722G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333870 | ||||||
chr16:23333919
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8-14673C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333919 | ||||||
chr16:23333924
|
GCCTAACT others(7): Show |
G | 1 | a0001c0001t0001g0161 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8-14663_-8-14650d others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23333924 | |||||
chr16:23333990
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-8-14602C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23333990 | ||||||
chr16:23334026
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-8-14566G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334026 | ||||||
chr16:23334041
|
C | T | 2 | a0002c0004t0001g0051a0002c0004t0001g0058 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-8-14551C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334041 | ||||||
chr16:23334206
|
C | T | 2 | a0002c0004t0001g0005a0003c0005t0001g0004 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-8-14386C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334206 | ||||||
chr16:23334230
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-14362C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334230 | ||||||
chr16:23334385
|
A | G | 34 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0099others(31): Show | 34 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.-8-14207A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334385 | ||||||
chr16:23334488
|
G | A | 1 | a0001c0002t0005g0233 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8-14104G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334488 | ||||||
chr16:23334500
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG01346.hp2 HG02135.hp1 HG03239.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-14092C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334500 | ||||||
chr16:23334557
|
G | A | 19 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(16): Show | 19 | HG00639.hp2 HG01934.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-14035G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334557 | ||||||
chr16:23334565
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-8-14027T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334565 | ||||||
chr16:23334573
|
T | G | 1 | a0001c0002t0001g0302 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-8-14019T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334573 | ||||||
chr16:23334617
|
T | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(64): Show | 67 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-8-13975T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334617 | ||||||
chr16:23334744
|
C | T | 17 | a0001c0001t0001g0108a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-13848C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334744 | ||||||
chr16:23334809
|
G | A | 2 | a0001c0003t0001g0139a0001c0008t0001g0148 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-13783G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23334809 | ||||||
chr16:23335451
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0071a0001c0001t0001g0072others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-13141T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23335451 | ||||||
chr16:23335459
|
CT | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-8-13118delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23335459 | |||||
chr16:23335459
|
CTT | C | 39 | a0001c0001t0001g0041a0001c0001t0001g0104a0001c0001t0001g0117others(36): Show | 39 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-8-13119_-8-13118d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23335459 | |||||
chr16:23335717
|
G | A | 1 | a0001c0002t0001g0302 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-8-12875G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23335717 | ||||||
chr16:23335722
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(149): Show | 152 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-8-12870T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23335722 | ||||||
chr16:23335750
|
A | AT | 20 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0124others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8-12830dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23335750 | |||||
chr16:23335750
|
AT | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0092others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8-12830delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23335750 | |||||
chr16:23335750
|
ATTT | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(20): Show | 23 | HG01346.hp2 HG02135.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8-12832_-8-12830d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23335750 | |||||
chr16:23335799
|
C | T | 19 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0280others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-12793C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23335799 | ||||||
chr16:23335983
|
A | G | 71 | a0001c0001t0001g0041a0001c0001t0001g0092a0001c0001t0001g0093others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-8-12609A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23335983 | ||||||
chr16:23336010
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0251others(1): Show | 4 | HG01123.hp2 HG02055.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-12582G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336010 | ||||||
chr16:23336112
|
A | G | 1 | a0001c0002t0001g0235 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-8-12480A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336112 | ||||||
chr16:23336161
|
T | C | 42 | a0001c0001t0001g0041a0001c0001t0001g0100a0001c0001t0001g0104others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-12431T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336161 | ||||||
chr16:23336202
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0162others(1): Show | 4 | NA18979.hp2 NA18980.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-12390T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336202 | ||||||
chr16:23336371
|
A | AT | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0097others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-12202dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23336371 | |||||
chr16:23336371
|
A | ATT | 41 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0118others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-8-12203_-8-12202d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23336371 | |||||
chr16:23336371
|
A | ATTT | 23 | a0001c0001t0001g0041a0001c0001t0001g0104a0001c0001t0001g0130others(20): Show | 23 | HG01192.hp2 HG01934.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8-12204_-8-12202d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23336371 | |||||
chr16:23336371
|
AT | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(55): Show | 58 | HG00735.hp1 HG01109.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.-8-12202delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23336371 | |||||
chr16:23336371
|
ATT | A | 25 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0111others(22): Show | 25 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-12203_-8-12202d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23336371 | |||||
chr16:23336519
|
G | A | 19 | a0001c0001t0001g0137a0001c0001t0001g0268a0001c0001t0001g0269others(16): Show | 19 | HG00639.hp2 HG01934.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-12073G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336519 | ||||||
chr16:23336560
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG01167.hp2 HG01346.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-8-12032C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336560 | ||||||
chr16:23336622
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8-11970G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336622 | ||||||
chr16:23336662
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8-11930G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336662 | ||||||
chr16:23336690
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0284 | 3 | HG02055.hp1 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-11902G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336690 | ||||||
chr16:23336803
|
T | G | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-11789T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336803 | ||||||
chr16:23336930
|
G | A | 51 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0096others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-8-11662G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23336930 | ||||||
chr16:23337245
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8-11347G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337245 | ||||||
chr16:23337370
|
C | T | 19 | a0001c0001t0001g0137a0001c0001t0001g0268a0001c0001t0001g0269others(16): Show | 19 | HG00639.hp2 HG01934.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-11222C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337370 | ||||||
chr16:23337374
|
C | CT | 148 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(145): Show | 148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-8-11202dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23337374 | |||||
chr16:23337374
|
C | CTT | 8 | a0001c0001t0001g0034a0001c0001t0001g0110a0001c0001t0001g0303others(5): Show | 8 | HG01169.hp1 HG01346.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-11203_-8-11202d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23337374 | |||||
chr16:23337374
|
C | CTTT | 16 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG02135.hp1 HG03239.hp2 HG03834.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-11204_-8-11202d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23337374 | |||||
chr16:23337374
|
CT | C | 6 | a0001c0001t0001g0085a0001c0001t0001g0186a0001c0001t0001g0228others(3): Show | 6 | HG02145.hp1 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-11202delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23337374 | |||||
chr16:23337393
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-11199G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337393 | ||||||
chr16:23337443
|
G | A | 21 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(18): Show | 21 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-11149G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337443 | ||||||
chr16:23337490
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-11102G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337490 | ||||||
chr16:23337657
|
C | A | 19 | a0001c0001t0001g0137a0001c0001t0001g0268a0001c0001t0001g0269others(16): Show | 19 | HG00639.hp2 HG01934.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-10935C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337657 | ||||||
chr16:23337749
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-8-10843A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337749 | ||||||
chr16:23337842
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-8-10750G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337842 | ||||||
chr16:23337933
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-8-10659C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23337933 | ||||||
chr16:23338117
|
C | T | 2 | a0001c0001t0001g0267a0001c0003t0001g0274 | 2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-8-10475C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23338117 | ||||||
chr16:23338347
|
C | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0088others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-8-10245C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23338347 | ||||||
chr16:23338455
|
G | A | 3 | a0001c0003t0001g0083a0002c0004t0001g0082a0002c0004t0001g0151 | 3 | HG02630.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-10137G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23338455 | ||||||
chr16:23338640
|
A | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0116others(5): Show | 8 | HG01168.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-9952A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23338640 | ||||||
chr16:23338647
|
G | C | 1 | a0001c0002t0001g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8-9945G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23338647 | ||||||
chr16:23338976
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(40): Show | 43 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.-8-9616A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23338976 | ||||||
chr16:23339195
|
T | A | 17 | a0001c0001t0001g0108a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-9397T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339195 | ||||||
chr16:23339292
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(39): Show | 42 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-9300T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339292 | ||||||
chr16:23339348
|
A | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(39): Show | 42 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-9244A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339348 | ||||||
chr16:23339413
|
CT | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-8-9168delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23339413 | |||||
chr16:23339501
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-8-9091G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339501 | ||||||
chr16:23339561
|
T | A | 66 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0072others(63): Show | 66 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8-9031T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339561 | ||||||
chr16:23339566
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-8-9026T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339566 | ||||||
chr16:23339580
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(39): Show | 42 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-9012T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339580 | ||||||
chr16:23339588
|
T | A | 3 | a0001c0003t0001g0083a0002c0004t0001g0082a0002c0004t0001g0151 | 3 | HG02630.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-9004T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339588 | ||||||
chr16:23339759
|
G | A | 34 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(31): Show | 34 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.-8-8833G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339759 | ||||||
chr16:23339828
|
A | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0088others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-8-8764A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339828 | ||||||
chr16:23339857
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(25): Show | 28 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-8735G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339857 | ||||||
chr16:23339902
|
G | T | 1 | a0001c0001t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8-8690G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23339902 | ||||||
chr16:23340361
|
A | G | 3 | a0001c0003t0001g0083a0002c0004t0001g0082a0002c0004t0001g0151 | 3 | HG02630.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-8231A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23340361 | ||||||
chr16:23340541
|
C | CT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(25): Show | 28 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-8045dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23340541 | |||||
chr16:23340611
|
G | T | 42 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0016others(39): Show | 42 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-7981G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23340611 | ||||||
chr16:23340638
|
C | A | 65 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0016others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-8-7954C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23340638 | ||||||
chr16:23340891
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-8-7701C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23340891 | ||||||
chr16:23340897
|
A | AGT | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(27): Show | 30 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-7677_-8-7676dup others(2): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23340897 | |||||
chr16:23340897
|
AGT | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.-8-7677_-8-7676del others(2): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23340897 | |||||
chr16:23341522
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-8-7070C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23341522 | ||||||
chr16:23341527
|
G | A | 118 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(115): Show | 118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-8-7065G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23341527 | ||||||
chr16:23341647
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-8-6945A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23341647 | ||||||
chr16:23341771
|
G | A | 1 | a0001c0008t0001g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8-6821G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23341771 | ||||||
chr16:23341798
|
G | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(25): Show | 28 | HG00544.hp1 HG00735.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-6794G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23341798 | ||||||
chr16:23341969
|
T | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034 | 3 | HG01168.hp1 HG01169.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-8-6623T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23341969 | ||||||
chr16:23342020
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-6572A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342020 | ||||||
chr16:23342271
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-6321G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342271 | ||||||
chr16:23342272
|
AGTTTCAC others(10): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-6319_-8-6303del others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342272 | ||||||
chr16:23342304
|
G | A | 20 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0280others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-6288G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342304 | ||||||
chr16:23342666
|
G | GA | 7 | a0001c0001t0001g0022a0001c0001t0001g0241a0001c0002t0001g0185others(4): Show | 7 | HG00544.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-5915dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23342666 | |||||
chr16:23342666
|
GA | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(32): Show | 35 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-8-5915delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23342666 | |||||
chr16:23342737
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-8-5855G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342737 | ||||||
chr16:23342760
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-5832G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342760 | ||||||
chr16:23342783
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8-5809T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23342783 | ||||||
chr16:23343154
|
C | T | 2 | a0001c0008t0001g0148a0001c0008t0001g0291 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-8-5438C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343154 | ||||||
chr16:23343170
|
C | T | 3 | a0001c0003t0001g0083a0002c0004t0001g0082a0002c0004t0001g0151 | 3 | HG02630.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-5422C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343170 | ||||||
chr16:23343207
|
C | A | 30 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(27): Show | 30 | HG00639.hp2 HG01109.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-5385C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343207 | ||||||
chr16:23343208
|
G | A | 3 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0008t0003g0091 | 3 | HG01891.hp1 HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-8-5384G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343208 | ||||||
chr16:23343281
|
CG | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0016others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.-8-5310delG | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343281 | ||||||
chr16:23343327
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | NA18959.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-8-5265C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343327 | ||||||
chr16:23343408
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-5184C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343408 | ||||||
chr16:23343464
|
GGAAA | G | 31 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(28): Show | 31 | HG00639.hp2 HG01109.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-5127_-8-5124del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343464 | ||||||
chr16:23343465
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-8-5127G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343465 | ||||||
chr16:23343470
|
G | A | 31 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(28): Show | 31 | HG00639.hp2 HG01109.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-5122G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343470 | ||||||
chr16:23343471
|
A | AAAGGAAG others(5): Show |
1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-5118_-8-5117ins others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343471 | |||||
chr16:23343471
|
A | AAAGGAAG others(9): Show |
1 | a0001c0003t0001g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-5118_-8-5117ins others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343471 | |||||
chr16:23343471
|
AAAGAAAG others(5): Show |
A | 2 | a0001c0001t0001g0299a0001c0001t0002g0042 | 2 | HG01934.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-8-5117_-8-5106del others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343471 | |||||
chr16:23343475
|
A | AAAGG | 45 | a0001c0001t0001g0014a0001c0001t0001g0085a0001c0001t0001g0088others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8-5086_-8-5083dup others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | AAAGGAAG others(1): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0161a0001c0003t0001g0159 | 3 | HG01074.hp1 HG04184.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-8-5090_-8-5083dup others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | AAAGGAAG others(5): Show |
1 | a0001c0008t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-8-5094_-8-5083dup others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | AAAGGAAG others(9): Show |
5 | a0001c0001t0001g0149a0001c0001t0002g0020a0001c0003t0001g0133others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-5098_-8-5083dup others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | AAAGGAAG others(17): Show |
1 | a0001c0001t0001g0003 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8-5106_-8-5083dup others(24): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | AAAGGAAG others(21): Show |
1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-8-5110_-8-5083dup others(28): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | AAAGGAAG others(25): Show |
2 | a0001c0001t0001g0001a0001c0001t0001g0108 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-5114_-8-5083dup others(32): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
A | G | 3 | a0001c0001t0001g0098a0001c0003t0001g0064a0003c0005t0001g0066 | 3 | HG01891.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-8-5117A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343475 | ||||||
chr16:23343475
|
AAAGG | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00438.hp1 HG01346.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.-8-5086_-8-5083del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343475
|
AAAGGAAG others(5): Show |
A | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-8-5094_-8-5083del others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343475 | |||||
chr16:23343486
|
G | GGAAGGAA others(24): Show |
9 | a0001c0001t0001g0280a0001c0001t0001g0285a0001c0001t0001g0286others(6): Show | 9 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-5083_-8-5082ins others(31): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343486 | |||||
chr16:23343486
|
G | GGAAGGAA others(28): Show |
5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0297others(2): Show | 5 | HG02723.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-5083_-8-5082ins others(35): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343486 | |||||
chr16:23343486
|
G | GGAAGGAA others(32): Show |
1 | a0001c0001t0007g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8-5083_-8-5082ins others(39): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343486 | |||||
chr16:23343487
|
GAAGGAAG others(15): Show |
G | 5 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0019others(2): Show | 5 | HG01099.hp1 HG02071.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5085_-8-5064del others(22): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343487 | |||||
chr16:23343491
|
G | GAAGGAAG others(7): Show |
1 | a0003c0005t0001g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8-5100_-8-5087dup others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343491 | |||||
chr16:23343491
|
GAAGGAAG others(11): Show |
G | 33 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0028others(30): Show | 33 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.-8-5082_-8-5065del others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343491 | |||||
chr16:23343495
|
GAAGGAAG others(7): Show |
G | 1 | a0001c0002t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-8-5082_-8-5069del others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343495 | |||||
chr16:23343529
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-8-5063A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343529 | ||||||
chr16:23343531
|
A | AGAGG | 16 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(13): Show | 16 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-5046_-8-5043dup others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343531 | |||||
chr16:23343535
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8-5057G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343535 | ||||||
chr16:23343581
|
G | GAGAA | 35 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0055others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-8-4945_-8-4942dup others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
G | GAGAAAGA others(1): Show |
18 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0096others(15): Show | 18 | HG00544.hp1 HG01258.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8-4949_-8-4942dup others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
G | GAGAAAGA others(5): Show |
12 | a0001c0001t0001g0170a0001c0001t0001g0179a0001c0001t0001g0197others(9): Show | 12 | HG00140.hp1 HG01081.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-4953_-8-4942dup others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
G | GAGAAAGA others(9): Show |
5 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0263others(2): Show | 5 | HG01099.hp2 HG01109.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-4957_-8-4942dup others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
G | GAGAAAGA others(13): Show |
1 | a0001c0001t0001g0236 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-8-4961_-8-4942dup others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAA | G | 28 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0149others(25): Show | 28 | HG00544.hp2 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-4945_-8-4942del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(1): Show |
G | 21 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0112others(18): Show | 21 | HG01070.hp2 HG01255.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-4949_-8-4942del others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(5): Show |
G | 16 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0070others(13): Show | 16 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-4953_-8-4942del others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(9): Show |
G | 11 | a0001c0001t0001g0012a0001c0001t0001g0141a0001c0001t0001g0154others(8): Show | 11 | HG00099.hp2 HG01106.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-4957_-8-4942del others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(13): Show |
G | 3 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0173 | 3 | HG01884.hp1 NA19085.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-8-4961_-8-4942del others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(17): Show |
G | 4 | a0001c0001t0001g0071a0001c0001t0001g0101a0001c0001t0001g0248others(1): Show | 4 | HG02698.hp1 HG02717.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-4965_-8-4942del others(24): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(21): Show |
G | 3 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0158 | 3 | HG02698.hp2 HG04115.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-8-4969_-8-4942del others(28): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(25): Show |
G | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0041others(4): Show | 7 | NA18955.hp1 NA18955.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-4973_-8-4942del others(32): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343581
|
GAGAAAGA others(29): Show |
G | 28 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(25): Show | 28 | HG00438.hp1 HG01346.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8-4977_-8-4942del others(36): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343581 | |||||
chr16:23343584
|
AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0001g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-5005_-8-4995del others(11): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343584 | |||||
chr16:23343597
|
A | AAGAAAGA others(43): Show |
1 | a0001c0008t0001g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8-4993_-8-4944dup others(50): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343597 | |||||
chr16:23343597
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-4995A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343597 | ||||||
chr16:23343600
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-8-4992A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343600 | ||||||
chr16:23343606
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0019 | 2 | NA18957.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-8-4986A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343606 | ||||||
chr16:23343609
|
A | AAGAAAGA others(31): Show |
1 | a0001c0008t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-8-4981_-8-4944dup others(38): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343609 | |||||
chr16:23343609
|
A | AAGAAAGA others(35): Show |
1 | a0001c0008t0003g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8-4942_-8-4941ins others(42): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343609 | |||||
chr16:23343627
|
G | A | 2 | a0001c0001t0001g0062a0002c0004t0001g0151 | 2 | HG03579.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-8-4965G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343627 | ||||||
chr16:23343631
|
GAAAGAAA others(13): Show |
G | 2 | a0001c0001t0001g0062a0002c0004t0001g0151 | 2 | HG03579.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-8-4952_-8-4933del others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343631 | |||||
chr16:23343635
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-4957G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343635 | ||||||
chr16:23343639
|
G | A | 8 | a0001c0001t0001g0053a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 8 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-4953G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343639 | ||||||
chr16:23343639
|
GAAAGAAA others(5): Show |
G | 1 | a0001c0001t0001g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-4944_-8-4933del others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343639 | |||||
chr16:23343643
|
G | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0001g0286others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-4949G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343643 | ||||||
chr16:23343643
|
GAAAGAAA others(1): Show |
G | 8 | a0001c0001t0001g0053a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 8 | HG02622.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-4941_-8-4934del others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343643 | |||||
chr16:23343647
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0049others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-4945G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343647 | ||||||
chr16:23343647
|
GAAAA | G | 6 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0001g0286others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-4941_-8-4938del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343647 | |||||
chr16:23343648
|
A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0250 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-8-4942_-8-4941ins others(15): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343648 | |||||
chr16:23343649
|
A | AAGAAAGA others(7): Show |
1 | a0001c0001t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-4942_-8-4941ins others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343649 | |||||
chr16:23343651
|
A | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(35): Show | 38 | HG00323.hp1 HG00408.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8-4941A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343651 | ||||||
chr16:23343656
|
A | AAAAAAAG others(5): Show |
13 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0052others(10): Show | 13 | HG01123.hp1 HG01167.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8-4934_-8-4933ins others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343656 | |||||
chr16:23343656
|
A | AAAGAAAA others(9): Show |
3 | a0001c0001t0001g0050a0001c0001t0001g0106a0001c0001t0001g0119 | 3 | HG00408.hp1 NA18977.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-8-4933_-8-4932ins others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343656 | |||||
chr16:23343656
|
A | AAAGAAAA others(8): Show |
1 | a0001c0001t0001g0132 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-8-4933_-8-4932ins others(15): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343656 | |||||
chr16:23343656
|
A | AAAGAAAG others(13): Show |
7 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0057others(4): Show | 7 | HG00323.hp1 HG02055.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-4933_-8-4932ins others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343656 | |||||
chr16:23343656
|
A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-8-4933_-8-4932ins others(19): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343656 | |||||
chr16:23343656
|
A | AAAGG | 29 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0019others(26): Show | 29 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-4924_-8-4921dup others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23343656 | |||||
chr16:23343656
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0028others(28): Show | 31 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8-4936A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343656 | ||||||
chr16:23343671
|
G | GGAAGA | 3 | a0001c0008t0001g0148a0001c0008t0001g0291a0001c0008t0003g0091 | 3 | HG02486.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-8-4921_-8-4920ins others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343671 | ||||||
chr16:23343715
|
A | T | 26 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0116others(23): Show | 26 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-4877A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23343715 | ||||||
chr16:23344087
|
C | T | 3 | a0001c0003t0001g0083a0002c0004t0001g0082a0002c0004t0001g0151 | 3 | HG02630.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-4505C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344087 | ||||||
chr16:23344091
|
T | C | 24 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0116others(21): Show | 24 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-4501T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344091 | ||||||
chr16:23344372
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-8-4220A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344372 | ||||||
chr16:23344629
|
G | T | 1 | a0003c0005t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-3963G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344629 | ||||||
chr16:23344764
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0096others(35): Show | 38 | HG00140.hp2 HG00323.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8-3828C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344764 | ||||||
chr16:23344872
|
T | C | 5 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0003t0001g0083others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3720T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344872 | ||||||
chr16:23344894
|
T | C | 1 | a0002c0004t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8-3698T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344894 | ||||||
chr16:23344971
|
G | A | 4 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 4 | HG01258.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-3621G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344971 | ||||||
chr16:23344980
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0096others(35): Show | 38 | HG00140.hp2 HG00323.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8-3612C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344980 | ||||||
chr16:23344991
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-8-3601C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23344991 | ||||||
chr16:23345009
|
A | AAG | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(71): Show | 74 | HG00438.hp1 HG00639.hp2 HG01109.hp1 others(71): Show |
intron_variant | MODIFIER | c.-8-3561_-8-3560dup others(2): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23345009 | |||||
chr16:23345009
|
AAGAG | A | 5 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0003t0001g0083others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3563_-8-3560del others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23345009 | |||||
chr16:23345122
|
A | G | 31 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(28): Show | 31 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-3470A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345122 | ||||||
chr16:23345180
|
C | T | 5 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0003t0001g0083others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3412C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345180 | ||||||
chr16:23345337
|
T | C | 2 | a0001c0001t0001g0272a0001c0003t0001g0090 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8-3255T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345337 | ||||||
chr16:23345502
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0300a0001c0001t0001g0303others(3): Show | 6 | HG03239.hp2 HG03834.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3090G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345502 | ||||||
chr16:23345550
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-8-3042G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345550 | ||||||
chr16:23345552
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-8-3040T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345552 | ||||||
chr16:23345729
|
G | A | 4 | a0001c0001t0001g0085a0001c0001t0001g0271a0001c0001t0004g0086others(1): Show | 4 | HG02145.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2863G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345729 | ||||||
chr16:23345736
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8-2856G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345736 | ||||||
chr16:23345816
|
C | G | 19 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 19 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-2776C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345816 | ||||||
chr16:23345976
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-8-2616C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23345976 | ||||||
chr16:23346022
|
G | A | 5 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0003t0001g0083others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2570G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346022 | ||||||
chr16:23346103
|
C | T | 6 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-2489C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346103 | ||||||
chr16:23346144
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0251others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-2448G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346144 | ||||||
chr16:23346168
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8-2424T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346168 | ||||||
chr16:23346200
|
C | CT | 17 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0043others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-2363dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTT | 6 | a0001c0001t0001g0057a0001c0002t0001g0252a0001c0003t0001g0083others(3): Show | 6 | HG02258.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-2364_-8-2363dup others(2): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTT | 40 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0071others(37): Show | 40 | HG00639.hp2 HG01074.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-8-2365_-8-2363dup others(3): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTT | 36 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0026others(33): Show | 36 | HG00140.hp2 HG01106.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.-8-2366_-8-2363dup others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTT | 23 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0044others(20): Show | 23 | HG00438.hp1 HG02040.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-2367_-8-2363dup others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTT | 8 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0096others(5): Show | 8 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-2368_-8-2363dup others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTTT | 9 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0280others(6): Show | 9 | HG00323.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-2369_-8-2363dup others(7): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0108a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2373_-8-2363dup others(11): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0001g0085a0001c0001t0001g0138a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp1 HG01168.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-2374_-8-2363dup others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0145others(2): Show | 5 | HG01993.hp1 HG06807.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2375_-8-2363dup others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0119a0001c0001t0001g0210 | 2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-8-2376_-8-2363dup others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8-2382_-8-2363dup others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0124others(4): Show | 7 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-2374_-8-2363del others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346200
|
CTTTTTTT others(6): Show |
C | 76 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 76 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2375_-8-2363del others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346200 | |||||
chr16:23346234
|
C | T | 50 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(47): Show | 50 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.-8-2358C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346234 | ||||||
chr16:23346278
|
C | A | 19 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 19 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-2314C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346278 | ||||||
chr16:23346286
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-2306A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346286 | ||||||
chr16:23346354
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0088others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.-8-2238G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346354 | ||||||
chr16:23346458
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(38): Show | 41 | HG00438.hp1 HG01123.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.-8-2134G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346458 | ||||||
chr16:23346569
|
C | G | 1 | a0001c0002t0001g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-2023C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346569 | ||||||
chr16:23346594
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(38): Show | 41 | HG00438.hp1 HG01123.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.-8-1998G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346594 | ||||||
chr16:23346612
|
T | C | 3 | a0001c0008t0001g0148a0001c0008t0001g0291a0001c0008t0003g0091 | 3 | HG02486.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-8-1980T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346612 | ||||||
chr16:23346656
|
TTGCAGGC others(14): Show |
T | 19 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 19 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-1896_-8-1876del others(21): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 23346656 | |||||
chr16:23346727
|
C | T | 31 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(28): Show | 31 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-1865C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346727 | ||||||
chr16:23346888
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-8-1704C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23346888 | ||||||
chr16:23347132
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0251 | 3 | HG01123.hp2 HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-8-1460A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23347132 | ||||||
chr16:23347345
|
C | T | 5 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0003t0001g0083others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1247C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23347345 | ||||||
chr16:23347531
|
A | G | 40 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0096others(37): Show | 40 | HG00140.hp2 HG00323.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-8-1061A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23347531 | ||||||
chr16:23347640
|
G | C | 1 | a0001c0001t0001g0024 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-8-952G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23347640 | ||||||
chr16:23347733
|
C | A | 1 | a0003c0005t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-859C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23347733 | ||||||
chr16:23347873
|
C | A | 1 | a0001c0002t0001g0235 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-8-719C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23347873 | ||||||
chr16:23348260
|
G | A | 3 | a0001c0008t0001g0148a0001c0008t0001g0291a0001c0008t0003g0091 | 3 | HG02486.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-8-332G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348260 | ||||||
chr16:23348266
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-8-326A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348266 | ||||||
chr16:23348292
|
T | C | 2 | a0001c0003t0001g0083a0002c0004t0001g0082 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-8-300T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348292 | ||||||
chr16:23348376
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-8-216A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348376 | ||||||
chr16:23348396
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-8-196T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348396 | ||||||
chr16:23348495
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0019 | 2 | NA18957.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-8-97G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348495 | ||||||
chr16:23348505
|
C | T | 2 | a0001c0003t0001g0133a0002c0004t0001g0005 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-8-87C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348505 | ||||||
chr16:23348519
|
T | C | 5 | a0001c0001t0001g0098a0001c0003t0001g0064a0001c0003t0001g0083others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-73T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 1/12 | chr16 | 23348519 | ||||||
chr16:23348953
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.311+43G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23348953 | ||||||
chr16:23349122
|
T | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0021others(32): Show | 35 | HG00438.hp1 HG01346.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.311+212T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23349122 | ||||||
chr16:23349544
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.311+634T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23349544 | ||||||
chr16:23349700
|
T | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.311+790T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23349700 | ||||||
chr16:23349819
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0251others(3): Show | 6 | HG01123.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.311+909C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23349819 | ||||||
chr16:23350040
|
T | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0061others(3): Show | 6 | HG02056.hp1 NA18980.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+1130T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350040 | ||||||
chr16:23350056
|
C | A | 29 | a0001c0001t0001g0035a0001c0001t0001g0085a0001c0001t0001g0109others(26): Show | 29 | HG00544.hp1 HG00639.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.311+1146C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350056 | ||||||
chr16:23350198
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.311+1288T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350198 | ||||||
chr16:23350212
|
C | A | 2 | a0001c0001t0001g0098a0001c0003t0001g0064 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.311+1302C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350212 | ||||||
chr16:23350267
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.311+1357C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350267 | ||||||
chr16:23350321
|
C | T | 23 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(20): Show | 23 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.311+1411C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350321 | ||||||
chr16:23350409
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0277 | 2 | HG02040.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.311+1499G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350409 | ||||||
chr16:23350509
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 116 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.311+1599T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350509 | ||||||
chr16:23350532
|
T | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.311+1622T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350532 | ||||||
chr16:23350538
|
A | G | 1 | a0001c0003t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.311+1628A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350538 | ||||||
chr16:23350660
|
C | T | 23 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0001g0120others(20): Show | 23 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.311+1750C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350660 | ||||||
chr16:23350661
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.311+1751T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350661 | ||||||
chr16:23350710
|
C | T | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.311+1800C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350710 | ||||||
chr16:23350783
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.311+1873C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350783 | ||||||
chr16:23350836
|
T | G | 87 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.311+1926T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350836 | ||||||
chr16:23350962
|
C | T | 1 | a0001c0006t0001g0247 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.312-1839C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23350962 | ||||||
chr16:23351249
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0282a0001c0001t0007g0290 | 3 | HG02622.hp1 NA18953.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.312-1552G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351249 | ||||||
chr16:23351295
|
G | A | 7 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0285others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.312-1506G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351295 | ||||||
chr16:23351357
|
T | C | 87 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.312-1444T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351357 | ||||||
chr16:23351399
|
C | T | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.312-1402C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351399 | ||||||
chr16:23351418
|
A | G | 37 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0096others(34): Show | 37 | HG00140.hp2 HG00323.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.312-1383A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351418 | ||||||
chr16:23351680
|
G | A | 1 | a0001c0002t0001g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.312-1121G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351680 | ||||||
chr16:23351875
|
CT | C | 19 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0084others(16): Show | 19 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.312-925delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23351875 | ||||||
chr16:23352037
|
T | C | 15 | a0001c0001t0001g0108a0001c0001t0001g0280a0001c0001t0001g0281others(12): Show | 15 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.312-764T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352037 | ||||||
chr16:23352078
|
A | T | 70 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0021others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.312-723A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352078 | ||||||
chr16:23352178
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.312-623C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352178 | ||||||
chr16:23352457
|
C | T | 4 | a0001c0001t0001g0143a0001c0008t0001g0148a0001c0008t0001g0291others(1): Show | 4 | HG02486.hp1 HG02630.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-344C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352457 | ||||||
chr16:23352498
|
C | G | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.312-303C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352498 | ||||||
chr16:23352594
|
G | A | 3 | a0001c0008t0001g0148a0001c0008t0001g0291a0001c0008t0003g0091 | 3 | HG02486.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.312-207G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352594 | ||||||
chr16:23352760
|
A | C | 135 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(132): Show | 135 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.312-41A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352760 | ||||||
chr16:23352765
|
C | A | 1 | a0001c0003t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.312-36C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 2/12 | chr16 | 23352765 | ||||||
chr16:23353302
|
A | C | 2 | a0001c0001t0001g0001a0001c0003t0001g0266 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.585+228A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353302 | ||||||
chr16:23353454
|
G | C | 1 | a0001c0002t0001g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.585+380G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353454 | ||||||
chr16:23353472
|
T | C | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.585+398T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353472 | ||||||
chr16:23353601
|
A | G | 12 | a0001c0001t0001g0072a0001c0001t0001g0137a0001c0001t0001g0268others(9): Show | 12 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+527A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353601 | ||||||
chr16:23353602
|
T | C | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.585+528T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353602 | ||||||
chr16:23353782
|
T | G | 40 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0088others(37): Show | 40 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.585+708T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353782 | ||||||
chr16:23353854
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.585+780G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23353854 | ||||||
chr16:23354412
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.586-887T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354412 | ||||||
chr16:23354508
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.586-791G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354508 | ||||||
chr16:23354519
|
C | T | 1 | a0001c0002t0001g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.586-780C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354519 | ||||||
chr16:23354657
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586-642G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354657 | ||||||
chr16:23354716
|
G | A | 2 | a0001c0002t0001g0201a0001c0002t0001g0219 | 2 | HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.586-583G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354716 | ||||||
chr16:23354793
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.586-506G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354793 | ||||||
chr16:23354994
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.586-305C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23354994 | ||||||
chr16:23355101
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.586-198G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23355101 | ||||||
chr16:23355142
|
G | T | 14 | a0001c0001t0001g0108a0001c0001t0001g0138a0001c0001t0001g0251others(11): Show | 14 | HG01123.hp2 HG01168.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.586-157G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23355142 | ||||||
chr16:23355207
|
C | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0085a0001c0001t0001g0098others(29): Show | 32 | HG00544.hp1 HG00639.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-92C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23355207 | ||||||
chr16:23355210
|
C | T | 7 | a0001c0003t0001g0083a0001c0003t0001g0139a0001c0008t0001g0148others(4): Show | 7 | HG02486.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-89C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23355210 | ||||||
chr16:23355265
|
C | T | 1 | a0002c0004t0001g0005 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586-34C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 3/12 | chr16 | 23355265 | ||||||
chr16:23355530
|
C | T | 2 | a0001c0001t0001g0155a0001c0003t0001g0159 | 2 | HG01074.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.776+41C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23355530 | ||||||
chr16:23355551
|
G | A | 1 | a0001c0003t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.776+62G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23355551 | ||||||
chr16:23355591
|
C | T | 40 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0108others(37): Show | 40 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.776+102C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23355591 | ||||||
chr16:23355664
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.776+175C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23355664 | ||||||
chr16:23355700
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.776+211T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23355700 | ||||||
chr16:23355970
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0098others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.776+481A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23355970 | ||||||
chr16:23356037
|
T | C | 2 | a0001c0001t0001g0101a0001c0003t0001g0103 | 2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.776+548T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356037 | ||||||
chr16:23356052
|
T | C | 4 | a0001c0001t0001g0085a0001c0001t0001g0271a0001c0001t0004g0086others(1): Show | 4 | HG02145.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+563T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356052 | ||||||
chr16:23356095
|
G | A | 7 | a0001c0003t0001g0083a0001c0003t0001g0139a0001c0008t0001g0148others(4): Show | 7 | HG02486.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.776+606G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356095 | ||||||
chr16:23356259
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.776+770A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356259 | ||||||
chr16:23356270
|
C | T | 26 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0119others(23): Show | 26 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.776+781C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356270 | ||||||
chr16:23356295
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.776+806G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356295 | ||||||
chr16:23356623
|
CT | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.776+1136delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23356623 | |||||
chr16:23356625
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0175a0001c0001t0001g0260 | 3 | HG01123.hp1 HG02055.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.776+1136T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356625 | ||||||
chr16:23356631
|
A | C | 1 | a0001c0003t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.776+1142A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356631 | ||||||
chr16:23356635
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.776+1146A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356635 | ||||||
chr16:23356658
|
G | T | 7 | a0001c0003t0001g0083a0001c0003t0001g0139a0001c0008t0001g0148others(4): Show | 7 | HG02486.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.776+1169G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356658 | ||||||
chr16:23356873
|
G | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.776+1384G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23356873 | ||||||
chr16:23357160
|
A | G | 1 | a0002c0004t0001g0005 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.776+1671A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357160 | ||||||
chr16:23357244
|
C | G | 6 | a0001c0003t0001g0083a0001c0003t0001g0139a0001c0008t0001g0148others(3): Show | 6 | HG02486.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+1755C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357244 | ||||||
chr16:23357346
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.776+1857G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357346 | ||||||
chr16:23357439
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(89): Show | 92 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.776+1950C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357439 | ||||||
chr16:23357440
|
G | A | 1 | a0005c0016t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.776+1951G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357440 | ||||||
chr16:23357480
|
G | A | 5 | a0001c0003t0001g0133a0001c0003t0001g0293a0002c0004t0001g0151others(2): Show | 5 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+1991G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357480 | ||||||
chr16:23357498
|
G | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0280others(10): Show | 13 | HG01168.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.776+2009G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357498 | ||||||
chr16:23357524
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.776+2035A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357524 | ||||||
chr16:23357537
|
C | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0071others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.776+2048C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357537 | ||||||
chr16:23357538
|
G | A | 5 | a0001c0003t0001g0133a0001c0003t0001g0293a0002c0004t0001g0151others(2): Show | 5 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+2049G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357538 | ||||||
chr16:23357746
|
C | A | 25 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0119others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+2257C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357746 | ||||||
chr16:23357769
|
A | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.776+2280A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23357769 | ||||||
chr16:23358000
|
A | G | 1 | a0002c0004t0001g0005 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.776+2511A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358000 | ||||||
chr16:23358072
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.776+2583G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358072 | ||||||
chr16:23358100
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0138others(11): Show | 14 | HG01168.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.776+2611G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358100 | ||||||
chr16:23358112
|
G | A | 32 | a0001c0001t0001g0071a0001c0001t0001g0088a0001c0001t0001g0096others(29): Show | 32 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.776+2623G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358112 | ||||||
chr16:23358261
|
CA | C | 5 | a0001c0003t0001g0133a0001c0003t0001g0293a0002c0004t0001g0151others(2): Show | 5 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+2773delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358261 | ||||||
chr16:23358428
|
C | A | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.776+2939C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358428 | ||||||
chr16:23358600
|
T | C | 1 | a0001c0002t0001g0048 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.776+3111T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358600 | ||||||
chr16:23358642
|
C | T | 5 | a0001c0003t0001g0133a0001c0003t0001g0293a0002c0004t0001g0151others(2): Show | 5 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+3153C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358642 | ||||||
chr16:23358673
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.776+3184G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358673 | ||||||
chr16:23358702
|
T | A | 1 | a0001c0008t0001g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.776+3213T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358702 | ||||||
chr16:23358716
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.776+3227G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358716 | ||||||
chr16:23358734
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.776+3245C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358734 | ||||||
chr16:23358887
|
A | G | 9 | a0001c0003t0001g0074a0001c0003t0001g0077a0001c0003t0001g0078others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.776+3398A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358887 | ||||||
chr16:23358909
|
A | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0271a0001c0001t0004g0086others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+3420A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23358909 | ||||||
chr16:23359210
|
G | A | 19 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0001g0126others(16): Show | 19 | HG00741.hp2 HG01106.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.776+3721G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359210 | ||||||
chr16:23359336
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.776+3847C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359336 | ||||||
chr16:23359360
|
G | T | 2 | a0001c0001t0001g0132a0001c0002t0001g0172 | 2 | HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.776+3871G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359360 | ||||||
chr16:23359362
|
T | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0272a0001c0001t0001g0281others(3): Show | 6 | HG02055.hp1 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+3873T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359362 | ||||||
chr16:23359363
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.776+3874C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359363 | ||||||
chr16:23359386
|
C | T | 1 | a0001c0008t0003g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.776+3897C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359386 | ||||||
chr16:23359569
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.776+4080C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359569 | ||||||
chr16:23359709
|
AC | A | 9 | a0001c0003t0001g0074a0001c0003t0001g0077a0001c0003t0001g0078others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.776+4222delC | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23359709 | |||||
chr16:23359711
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.776+4222C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359711 | ||||||
chr16:23359789
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(203): Show | 206 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.776+4300C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359789 | ||||||
chr16:23359793
|
G | C | 1 | a0001c0002t0001g0193 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.776+4304G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359793 | ||||||
chr16:23359907
|
T | A | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.776+4418T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359907 | ||||||
chr16:23359969
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.776+4480G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23359969 | ||||||
chr16:23360076
|
G | A | 9 | a0001c0003t0001g0074a0001c0003t0001g0077a0001c0003t0001g0078others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.776+4587G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360076 | ||||||
chr16:23360141
|
T | C | 33 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0030others(30): Show | 33 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.776+4652T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360141 | ||||||
chr16:23360166
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.776+4677C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360166 | ||||||
chr16:23360201
|
A | AAAAAAT | 6 | a0001c0003t0001g0083a0001c0003t0001g0139a0001c0003t0001g0292others(3): Show | 6 | HG00639.hp2 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+4715_776+4716i others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360201 | |||||
chr16:23360201
|
A | AAAATAAA others(9): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0239 | 2 | HG01934.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.776+4719_776+4720i others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360201 | |||||
chr16:23360201
|
A | AAAATAAA others(5): Show |
6 | a0001c0001t0001g0158a0001c0002t0001g0185a0002c0004t0001g0005others(3): Show | 6 | HG02280.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+4728_776+4739d others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360201 | |||||
chr16:23360201
|
A | AAAATAAA others(9): Show |
17 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0145others(14): Show | 17 | HG00323.hp1 HG01358.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.776+4724_776+4739d others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360201 | |||||
chr16:23360201
|
A | AAAATAAA others(13): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0259 | 2 | HG01258.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.776+4720_776+4739d others(22): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360201 | |||||
chr16:23360201
|
A | AAAATAAA others(21): Show |
1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.776+4739_776+4740i others(30): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360201 | |||||
chr16:23360209
|
T | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.776+4720T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360209 | ||||||
chr16:23360209
|
T | TAAATAAA others(13): Show |
1 | a0001c0001t0001g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.776+4739_776+4740i others(22): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360209 | |||||
chr16:23360217
|
T | TAAATAAA others(9): Show |
9 | a0001c0003t0001g0074a0001c0003t0001g0077a0001c0003t0001g0078others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.776+4739_776+4740i others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360217 | |||||
chr16:23360225
|
T | C | 6 | a0001c0001t0001g0157a0001c0003t0001g0083a0001c0003t0001g0139others(3): Show | 6 | HG02109.hp1 HG02630.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.776+4736T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360225 | ||||||
chr16:23360233
|
T | C | 1 | a0002c0004t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776+4744T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360233 | ||||||
chr16:23360243
|
A | C | 16 | a0001c0001t0001g0072a0001c0001t0001g0096a0001c0001t0001g0138others(13): Show | 16 | HG01109.hp1 HG01168.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.776+4754A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360243 | ||||||
chr16:23360278
|
T | C | 5 | a0002c0004t0001g0005a0002c0004t0001g0082a0003c0005t0001g0065others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.776+4789T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360278 | ||||||
chr16:23360316
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG00738.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.776+4827G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360316 | ||||||
chr16:23360474
|
C | T | 3 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0282 | 3 | HG03453.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.776+4985C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360474 | ||||||
chr16:23360579
|
G | T | 14 | a0001c0001t0001g0072a0001c0001t0001g0096a0001c0001t0001g0154others(11): Show | 14 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.776+5090G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360579 | ||||||
chr16:23360591
|
G | GT | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(110): Show | 113 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.776+5124dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360591 | |||||
chr16:23360591
|
G | GTT | 15 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0036others(12): Show | 15 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.776+5123_776+5124d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360591 | |||||
chr16:23360591
|
GT | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0044others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.776+5124delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23360591 | |||||
chr16:23360618
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.776+5129C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360618 | ||||||
chr16:23360633
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.776+5144G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360633 | ||||||
chr16:23360788
|
T | C | 10 | a0001c0003t0001g0083a0001c0003t0001g0113a0001c0003t0001g0139others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+5299T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360788 | ||||||
chr16:23360789
|
G | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0029others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.776+5300G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360789 | ||||||
chr16:23360856
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.776+5367A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360856 | ||||||
chr16:23360888
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.776+5399G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360888 | ||||||
chr16:23360956
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.776+5467G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23360956 | ||||||
chr16:23361040
|
C | T | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.776+5551C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361040 | ||||||
chr16:23361041
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.776+5552G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361041 | ||||||
chr16:23361085
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.776+5596T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361085 | ||||||
chr16:23361092
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0029others(26): Show | 29 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.776+5603C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361092 | ||||||
chr16:23361206
|
G | A | 1 | a0002c0004t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776+5717G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361206 | ||||||
chr16:23361341
|
G | T | 9 | a0001c0001t0001g0072a0001c0001t0001g0096a0001c0001t0001g0267others(6): Show | 9 | HG01109.hp1 HG01934.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.776+5852G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361341 | ||||||
chr16:23361722
|
A | G | 1 | a0002c0004t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.777-6134A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361722 | ||||||
chr16:23361735
|
C | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0111others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.777-6121C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361735 | ||||||
chr16:23361914
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.777-5942A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361914 | ||||||
chr16:23361982
|
G | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0111others(8): Show | 11 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.777-5874G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361982 | ||||||
chr16:23361996
|
A | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0049a0001c0001t0001g0130 | 3 | NA19011.hp1 NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.777-5860A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23361996 | ||||||
chr16:23362032
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.777-5824T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362032 | ||||||
chr16:23362054
|
C | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0029others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.777-5802C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362054 | ||||||
chr16:23362098
|
A | G | 31 | a0001c0001t0001g0137a0001c0003t0001g0064a0001c0003t0001g0074others(28): Show | 31 | HG01074.hp1 HG01167.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.777-5758A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362098 | ||||||
chr16:23362141
|
T | C | 1 | a0001c0003t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.777-5715T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362141 | ||||||
chr16:23362329
|
CA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0070others(29): Show | 32 | HG00639.hp2 HG01167.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.777-5513delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23362329 | |||||
chr16:23362340
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.777-5516A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362340 | ||||||
chr16:23362590
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0030 | 2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.777-5266G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362590 | ||||||
chr16:23362634
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.777-5222G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362634 | ||||||
chr16:23362665
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00544.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.777-5191A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362665 | ||||||
chr16:23362686
|
A | C | 22 | a0001c0003t0001g0064a0001c0003t0001g0074a0001c0003t0001g0077others(19): Show | 22 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.777-5170A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362686 | ||||||
chr16:23362687
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.777-5169C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362687 | ||||||
chr16:23362693
|
G | C | 1 | a0001c0008t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.777-5163G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362693 | ||||||
chr16:23362704
|
TG | T | 4 | a0001c0003t0001g0293a0002c0007t0001g0087a0002c0007t0001g0283others(1): Show | 4 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-5150delG | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23362704 | |||||
chr16:23362709
|
C | T | 6 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0278others(3): Show | 6 | HG00639.hp2 HG02109.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.777-5147C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362709 | ||||||
chr16:23362731
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.777-5125C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362731 | ||||||
chr16:23362775
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.777-5081A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23362775 | ||||||
chr16:23363074
|
C | T | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.777-4782C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363074 | ||||||
chr16:23363075
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0029others(26): Show | 29 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.777-4781G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363075 | ||||||
chr16:23363171
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.777-4685C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363171 | ||||||
chr16:23363401
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0111others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.777-4455G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363401 | ||||||
chr16:23363607
|
G | A | 4 | a0001c0001t0001g0137a0001c0003t0001g0159a0001c0009t0001g0059others(1): Show | 4 | HG01074.hp1 HG01516.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-4249G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363607 | ||||||
chr16:23363792
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0030 | 2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.777-4064C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363792 | ||||||
chr16:23363892
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.777-3964G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23363892 | ||||||
chr16:23364010
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.777-3846T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364010 | ||||||
chr16:23364031
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.777-3825G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364031 | ||||||
chr16:23364396
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0178a0001c0001t0001g0197 | 3 | NA18944.hp1 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.777-3460G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364396 | ||||||
chr16:23364422
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.777-3434T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364422 | ||||||
chr16:23364424
|
G | GAGTGTTT others(3): Show |
1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.777-3427_777-3426i others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23364424 | |||||
chr16:23364428
|
G | A | 11 | a0001c0001t0001g0137a0001c0003t0001g0103a0001c0003t0001g0159others(8): Show | 11 | HG01074.hp1 HG01167.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.777-3428G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364428 | ||||||
chr16:23364600
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.777-3256A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364600 | ||||||
chr16:23364720
|
G | T | 2 | a0002c0004t0001g0051a0002c0004t0001g0058 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.777-3136G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23364720 | ||||||
chr16:23365019
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.777-2837G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365019 | ||||||
chr16:23365118
|
C | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0029others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.777-2738C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365118 | ||||||
chr16:23365170
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.777-2686T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365170 | ||||||
chr16:23365248
|
C | T | 2 | a0001c0001t0001g0046a0002c0004t0001g0040 | 2 | HG00639.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.777-2608C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365248 | ||||||
chr16:23365308
|
G | A | 8 | a0001c0001t0001g0109a0001c0001t0001g0173a0001c0002t0001g0172others(5): Show | 8 | HG01243.hp1 HG01255.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.777-2548G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365308 | ||||||
chr16:23365398
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.777-2458G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365398 | ||||||
chr16:23365449
|
GAGA | G | 10 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0116others(7): Show | 10 | HG00639.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-2404_777-2402d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365449 | |||||
chr16:23365483
|
A | AAAG | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.777-2367_777-2365d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365483 | |||||
chr16:23365483
|
AAAG | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0146a0001c0001t0001g0171others(1): Show | 4 | HG02129.hp1 HG02602.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-2367_777-2365d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365483 | |||||
chr16:23365489
|
GAAAAGAA others(3): Show |
G | 7 | a0001c0001t0001g0137a0001c0003t0001g0103a0001c0003t0001g0159others(4): Show | 7 | HG01074.hp1 HG01516.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.777-2354_777-2345d others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365489 | |||||
chr16:23365533
|
GAGAAGGA others(7): Show |
G | 1 | a0001c0003t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.777-2304_777-2291d others(16): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365533 | |||||
chr16:23365541
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.777-2315A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365541 | ||||||
chr16:23365543
|
GAGAAAGA others(11): Show |
G | 1 | a0001c0003t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.777-2304_777-2287d others(20): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365543 | |||||
chr16:23365547
|
AAGAAGGA others(3): Show |
A | 7 | a0001c0001t0001g0282a0001c0003t0001g0074a0001c0003t0001g0274others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.777-2304_777-2295d others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365547 | |||||
chr16:23365551
|
AGGAAAG | A | 12 | a0001c0001t0001g0072a0001c0001t0001g0213a0001c0001t0001g0269others(9): Show | 12 | HG01109.hp1 HG01167.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.777-2304_777-2299d others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365551 | ||||||
chr16:23365552
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.777-2304G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365552 | ||||||
chr16:23365555
|
AAG | A | 14 | a0001c0001t0001g0068a0001c0001t0001g0098a0001c0001t0001g0273others(11): Show | 14 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.777-2297_777-2296d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365555 | |||||
chr16:23365557
|
G | GAA | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.777-2298_777-2297i others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365557 | |||||
chr16:23365557
|
G | GAAAGAA | 19 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0063others(16): Show | 19 | HG00544.hp1 HG00735.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.777-2298_777-2297i others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365557 | |||||
chr16:23365567
|
G | GA | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0264 | 3 | HG00741.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.777-2286dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365567 | |||||
chr16:23365575
|
GAAAGAAA others(17): Show |
G | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.777-2279_777-2256d others(26): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365575 | |||||
chr16:23365583
|
GAAAGAGA others(1): Show |
G | 4 | a0002c0004t0001g0082a0003c0005t0001g0065a0003c0005t0001g0066others(1): Show | 4 | HG02896.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-2271_777-2264d others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365583 | |||||
chr16:23365583
|
GAAAGAGA others(5): Show |
G | 1 | a0002c0004t0001g0005 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.777-2271_777-2260d others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365583 | |||||
chr16:23365583
|
GAAAGAGA others(9): Show |
G | 44 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0035others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.777-2271_777-2256d others(18): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365583 | |||||
chr16:23365585
|
AAG | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0068others(55): Show | 58 | HG00140.hp1 HG00558.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.777-2267_777-2266d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365585 | |||||
chr16:23365587
|
G | GAA | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(94): Show | 97 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.777-2268_777-2267i others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365587 | |||||
chr16:23365587
|
G | GAAAGAAA others(3): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0118a0001c0001t0001g0158others(1): Show | 4 | HG03688.hp1 HG04115.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-2268_777-2267i others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365587 | |||||
chr16:23365587
|
G | GAGAA | 10 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0120others(7): Show | 10 | HG01106.hp1 HG02074.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.777-2239_777-2236d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365587 | |||||
chr16:23365587
|
G | GAGAAAGA others(1): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0173a0001c0002t0001g0038 | 3 | HG00099.hp1 HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.777-2243_777-2236d others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365587 | |||||
chr16:23365587
|
GAGAA | G | 7 | a0001c0001t0001g0089a0001c0001t0001g0208a0001c0001t0001g0240others(4): Show | 7 | HG00323.hp2 HG00438.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.777-2239_777-2236d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365587 | |||||
chr16:23365589
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0117others(1): Show | 4 | HG03710.hp2 NA18955.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-2267G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365589 | ||||||
chr16:23365589
|
GAAAGAAA others(4): Show |
G | 1 | a0001c0006t0001g0247 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.777-2266_777-2256d others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365589 | ||||||
chr16:23365591
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0112a0001c0001t0001g0114others(2): Show | 5 | HG03710.hp2 NA18955.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.777-2265A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365591 | ||||||
chr16:23365593
|
GAAAGAAA others(20): Show |
G | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.777-2252_777-2226d others(29): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365593 | |||||
chr16:23365601
|
GAA | G | 8 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0098others(5): Show | 8 | HG00438.hp1 HG01109.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.777-2253_777-2252d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365601 | |||||
chr16:23365603
|
A | AAG | 6 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0121others(3): Show | 6 | HG00544.hp1 NA18959.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.777-2251_777-2250d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365603 | |||||
chr16:23365603
|
A | AAGAGAG | 5 | a0001c0001t0001g0044a0001c0001t0001g0118a0001c0001t0001g0158others(2): Show | 5 | HG00408.hp2 HG03688.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.777-2250_777-2249i others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365603 | |||||
chr16:23365603
|
A | AAGAGAGA others(3): Show |
1 | a0001c0001t0001g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.777-2250_777-2249i others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365603 | |||||
chr16:23365605
|
GAA | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0021others(21): Show | 24 | HG00140.hp1 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.777-2249_777-2248d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365605 | |||||
chr16:23365605
|
GAAAGAAA others(8): Show |
G | 45 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0028others(42): Show | 45 | HG00738.hp1 HG01099.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.777-2240_777-2226d others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365605 | |||||
chr16:23365607
|
A | AAG | 36 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0049others(33): Show | 36 | HG00544.hp2 HG00735.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.777-2247_777-2246d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365607 | |||||
chr16:23365609
|
GAAAGAAA others(4): Show |
G | 4 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0117others(1): Show | 4 | HG03710.hp2 NA18955.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-2236_777-2226d others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365609 | |||||
chr16:23365615
|
A | G | 10 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0116others(7): Show | 10 | HG00639.hp2 HG01516.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-2241A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365615 | ||||||
chr16:23365616
|
AG | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0116others(7): Show | 10 | HG00639.hp2 HG01516.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-2239delG | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365616 | ||||||
chr16:23365617
|
G | GAGAAAGA others(4): Show |
7 | a0001c0001t0001g0129a0001c0001t0001g0143a0001c0001t0001g0206others(4): Show | 7 | HG00140.hp2 HG01081.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.777-2238_777-2237i others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365617 | |||||
chr16:23365617
|
G | GAGAAAGA others(8): Show |
1 | a0001c0001t0001g0003 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.777-2238_777-2237i others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365617 | |||||
chr16:23365617
|
G | GAGAGAGA others(12): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0043others(3): Show | 6 | HG02027.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.777-2238_777-2237i others(21): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365617 | |||||
chr16:23365617
|
G | GAGAGAGA others(16): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0167 | 2 | HG02717.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.777-2238_777-2237i others(25): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365617 | |||||
chr16:23365617
|
GAAA | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0035others(80): Show | 83 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.777-2235_777-2233d others(5): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23365617 | |||||
chr16:23365620
|
A | AG | 79 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(76): Show | 79 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.777-2236_777-2235i others(3): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAAAGAA others(31): Show |
1 | a0001c0001t0001g0264 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.777-2236_777-2235i others(40): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAAAGAA others(24): Show |
1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.777-2236_777-2235i others(33): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAAAGAA others(28): Show |
1 | a0001c0002t0001g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.777-2236_777-2235i others(37): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAAAGAG others(20): Show |
1 | a0001c0001t0001g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.777-2236_777-2235i others(29): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAAAGAG others(28): Show |
1 | a0001c0002t0001g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.777-2236_777-2235i others(37): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAGAAAG | 3 | a0001c0003t0001g0159a0001c0003t0001g0200a0001c0003t0001g0249 | 3 | HG01074.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.777-2236_777-2235i others(9): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAGAAAG others(8): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0057others(2): Show | 5 | HG01496.hp2 HG02071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.777-2236_777-2235i others(17): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAGAGAG others(16): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0150a0001c0001t0001g0306 | 3 | HG03669.hp1 HG03834.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.777-2236_777-2235i others(25): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | AGAGAGAG others(20): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0182others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-2236_777-2235i others(29): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365620
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0026others(25): Show | 28 | HG00140.hp2 HG00639.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.777-2236A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365620 | ||||||
chr16:23365806
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.777-2050C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365806 | ||||||
chr16:23365830
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.777-2026G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23365830 | ||||||
chr16:23366033
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.777-1823G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23366033 | ||||||
chr16:23366215
|
GT | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.777-1634delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23366215 | |||||
chr16:23366381
|
T | TTTTA | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.777-1471_777-1468d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 23366381 | |||||
chr16:23366451
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.777-1405C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23366451 | ||||||
chr16:23366517
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.777-1339C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23366517 | ||||||
chr16:23366771
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.777-1085A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23366771 | ||||||
chr16:23366967
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0220a0001c0001t0001g0239others(1): Show | 4 | HG00735.hp1 HG01081.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-889G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23366967 | ||||||
chr16:23367022
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.777-834G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367022 | ||||||
chr16:23367192
|
G | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.777-664G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367192 | ||||||
chr16:23367401
|
T | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.777-455T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367401 | ||||||
chr16:23367484
|
A | G | 23 | a0001c0003t0001g0064a0001c0003t0001g0074a0001c0003t0001g0077others(20): Show | 23 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.777-372A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367484 | ||||||
chr16:23367536
|
G | T | 3 | a0003c0005t0001g0065a0003c0005t0001g0066a0003c0005t0001g0075 | 3 | HG02976.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.777-320G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367536 | ||||||
chr16:23367545
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.777-311G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367545 | ||||||
chr16:23367670
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.777-186C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367670 | ||||||
chr16:23367750
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0004g0086 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.777-106C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367750 | ||||||
chr16:23367756
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.777-100G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367756 | ||||||
chr16:23367771
|
A | C | 1 | a0001c0002t0001g0218 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.777-85A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367771 | ||||||
chr16:23367814
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0239a0001c0012t0001g0196 | 3 | HG01081.hp2 HG01934.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.777-42C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367814 | ||||||
chr16:23367851
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.777-5T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 4/12 | chr16 | 23367851 | ||||||
chr16:23367977
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880+18G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23367977 | ||||||
chr16:23368056
|
A | AG | 89 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.880+103dupG | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 23368056 | |||||
chr16:23368125
|
C | G | 7 | a0001c0001t0001g0054a0001c0001t0001g0188a0001c0001t0001g0240others(4): Show | 7 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.880+166C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368125 | ||||||
chr16:23368158
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.880+199T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368158 | ||||||
chr16:23368167
|
C | T | 3 | a0001c0003t0001g0103a0001c0003t0001g0200a0001c0003t0001g0249 | 3 | HG01516.hp1 HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.880+208C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368167 | ||||||
chr16:23368348
|
G | T | 5 | a0001c0003t0001g0113a0001c0003t0001g0287a0001c0003t0001g0288others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+389G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368348 | ||||||
chr16:23368414
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.880+455T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368414 | ||||||
chr16:23368726
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.880+767A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368726 | ||||||
chr16:23368815
|
T | A | 10 | a0001c0003t0001g0103a0001c0003t0001g0159a0001c0003t0001g0200others(7): Show | 10 | HG01074.hp1 HG01167.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.880+856T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368815 | ||||||
chr16:23368881
|
A | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(1): Show | 4 | HG03453.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.880+922A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23368881 | ||||||
chr16:23369109
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.880+1150T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23369109 | ||||||
chr16:23369642
|
G | A | 4 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(1): Show | 4 | HG03453.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-1657G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23369642 | ||||||
chr16:23369654
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0033others(22): Show | 25 | HG00408.hp1 HG00741.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.881-1645C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23369654 | ||||||
chr16:23369764
|
G | T | 1 | a0001c0002t0001g0215 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.881-1535G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23369764 | ||||||
chr16:23369922
|
G | T | 1 | a0001c0001t0007g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.881-1377G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23369922 | ||||||
chr16:23370017
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.881-1282G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370017 | ||||||
chr16:23370057
|
A | C | 1 | a0001c0002t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.881-1242A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370057 | ||||||
chr16:23370154
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0282 | 3 | HG03453.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.881-1145G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370154 | ||||||
chr16:23370166
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0050others(4): Show | 7 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.881-1133C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370166 | ||||||
chr16:23370252
|
G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.881-1047G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370252 | ||||||
chr16:23370295
|
G | A | 4 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(1): Show | 4 | HG03453.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-1004G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370295 | ||||||
chr16:23370296
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(1): Show | 4 | HG03453.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-1003A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370296 | ||||||
chr16:23370503
|
C | T | 4 | a0001c0003t0001g0293a0002c0007t0001g0087a0002c0007t0001g0283others(1): Show | 4 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-796C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370503 | ||||||
chr16:23370593
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.881-706G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370593 | ||||||
chr16:23370940
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.881-359G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370940 | ||||||
chr16:23370999
|
G | A | 5 | a0002c0004t0001g0005a0002c0004t0001g0082a0003c0005t0001g0065others(2): Show | 5 | HG02280.hp1 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.881-300G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23370999 | ||||||
chr16:23371098
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.881-201G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23371098 | ||||||
chr16:23371123
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(2): Show | 5 | HG02145.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.881-176G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23371123 | ||||||
chr16:23371190
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.881-109C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23371190 | ||||||
chr16:23371213
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.881-86G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 5/12 | chr16 | 23371213 | ||||||
chr16:23371496
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0260 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1044+34T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/12 | chr16 | 23371496 | ||||||
chr16:23371503
|
G | A | 1 | a0007c0010t0001g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1044+41G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/12 | chr16 | 23371503 | ||||||
chr16:23371588
|
G | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0050others(5): Show | 8 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1044+126G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/12 | chr16 | 23371588 | ||||||
chr16:23371646
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1045-130C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/12 | chr16 | 23371646 | ||||||
chr16:23371661
|
CT | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1045-114delT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/12 | chr16 | 23371661 | ||||||
chr16:23371662
|
T | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0168others(1): Show | 4 | HG00544.hp1 HG03831.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-114T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 6/12 | chr16 | 23371662 | ||||||
chr16:23371926
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1152+43G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23371926 | ||||||
chr16:23372215
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1152+332G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372215 | ||||||
chr16:23372286
|
A | G | 5 | a0001c0003t0001g0113a0001c0003t0001g0287a0001c0003t0001g0288others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152+403A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372286 | ||||||
chr16:23372497
|
C | CT | 83 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1152+629dupT | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23372497 | |||||
chr16:23372550
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1152+667G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372550 | ||||||
chr16:23372572
|
G | A | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1152+689G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372572 | ||||||
chr16:23372619
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1152+736G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372619 | ||||||
chr16:23372723
|
G | A | 1 | a0002c0004t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1152+840G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372723 | ||||||
chr16:23372738
|
C | T | 1 | a0001c0003t0001g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1152+855C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372738 | ||||||
chr16:23372856
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1152+973T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372856 | ||||||
chr16:23372924
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1152+1041A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23372924 | ||||||
chr16:23372945
|
CA | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(46): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1152+1074delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23372945 | |||||
chr16:23373023
|
C | T | 1 | a0002c0004t0001g0082 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1152+1140C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373023 | ||||||
chr16:23373039
|
G | A | 1 | a0001c0002t0001g0045 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1152+1156G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373039 | ||||||
chr16:23373083
|
A | G | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1152+1200A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373083 | ||||||
chr16:23373084
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1152+1201G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373084 | ||||||
chr16:23373451
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1152+1568T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373451 | ||||||
chr16:23373497
|
C | G | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1152+1614C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373497 | ||||||
chr16:23373583
|
C | T | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1152+1700C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373583 | ||||||
chr16:23373674
|
G | A | 1 | a0001c0008t0003g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1152+1791G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373674 | ||||||
chr16:23373709
|
G | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(34): Show | 37 | HG00408.hp1 HG00408.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1152+1826G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373709 | ||||||
chr16:23373812
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1153-1926G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373812 | ||||||
chr16:23373874
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1153-1864G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373874 | ||||||
chr16:23373936
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0019others(16): Show | 19 | HG00408.hp1 HG00408.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1153-1802G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373936 | ||||||
chr16:23373985
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(26): Show | 29 | HG00408.hp1 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153-1753C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23373985 | ||||||
chr16:23374100
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1153-1638A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374100 | ||||||
chr16:23374220
|
C | T | 60 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0018others(57): Show | 60 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1153-1518C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374220 | ||||||
chr16:23374238
|
C | T | 1 | a0001c0009t0001g0191 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1153-1500C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374238 | ||||||
chr16:23374241
|
G | A | 8 | a0001c0001t0001g0109a0001c0001t0001g0173a0001c0002t0001g0172others(5): Show | 8 | HG01243.hp1 HG01255.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153-1497G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374241 | ||||||
chr16:23374268
|
G | GA | 6 | a0001c0001t0001g0046a0001c0001t0001g0092a0001c0001t0001g0149others(3): Show | 6 | HG01123.hp2 HG03098.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153-1449dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
G | GAAA | 20 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1153-1451_1153-144 others(7): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
G | GAAAAAAA | 11 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0128others(8): Show | 11 | HG00323.hp2 HG01346.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-1455_1153-144 others(11): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
G | GAAAAAAA others(1): Show |
96 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0018others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1153-1456_1153-144 others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
G | GAAAAAAA others(2): Show |
27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(24): Show | 27 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1153-1457_1153-144 others(13): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
G | GAAAAAAA others(3): Show |
1 | a0001c0002t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1153-1458_1153-144 others(14): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
G | GAAAAAAA others(8): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0192 | 2 | HG01361.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1153-1463_1153-144 others(19): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
GA | G | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0050others(12): Show | 15 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1153-1449delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
GAA | G | 25 | a0001c0001t0001g0096a0001c0001t0001g0213a0001c0001t0001g0284others(22): Show | 25 | HG01891.hp1 HG02074.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1153-1450_1153-144 others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374268
|
GAAAAAA | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0111others(9): Show | 12 | HG01074.hp1 HG01516.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1153-1454_1153-144 others(10): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374268 | |||||
chr16:23374290
|
G | A | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1153-1448G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374290 | ||||||
chr16:23374299
|
C | T | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1153-1439C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374299 | ||||||
chr16:23374314
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1153-1424C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374314 | ||||||
chr16:23374316
|
G | A | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1153-1422G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374316 | ||||||
chr16:23374335
|
A | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0053a0001c0001t0001g0105others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1153-1403A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374335 | ||||||
chr16:23374372
|
G | A | 2 | a0001c0001t0001g0158a0001c0002t0001g0185 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1153-1366G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374372 | ||||||
chr16:23374573
|
C | CA | 29 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0036others(26): Show | 29 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1153-1140dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374573 | |||||
chr16:23374573
|
CA | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0101others(21): Show | 24 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.1153-1140delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374573 | |||||
chr16:23374573
|
CAA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(29): Show | 32 | HG00408.hp1 HG00408.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1153-1141_1153-114 others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374573 | |||||
chr16:23374573
|
CAAAA | C | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1153-1143_1153-114 others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 23374573 | |||||
chr16:23374650
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(2): Show | 5 | HG02145.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-1088G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374650 | ||||||
chr16:23374781
|
G | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0026others(13): Show | 16 | HG00408.hp1 HG01167.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1153-957G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374781 | ||||||
chr16:23374823
|
A | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0030 | 2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1153-915A>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374823 | ||||||
chr16:23374826
|
A | G | 1 | a0001c0003t0001g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153-912A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374826 | ||||||
chr16:23374924
|
G | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0050others(1): Show | 4 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-814G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23374924 | ||||||
chr16:23375004
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1153-734A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375004 | ||||||
chr16:23375057
|
T | C | 1 | a0006c0014t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1153-681T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375057 | ||||||
chr16:23375113
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1153-625C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375113 | ||||||
chr16:23375113
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-625C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375113 | ||||||
chr16:23375114
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1153-624G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375114 | ||||||
chr16:23375134
|
C | T | 1 | a0003c0005t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1153-604C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375134 | ||||||
chr16:23375178
|
C | T | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1153-560C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375178 | ||||||
chr16:23375331
|
C | T | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1153-407C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375331 | ||||||
chr16:23375370
|
C | T | 1 | a0001c0003t0001g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153-368C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375370 | ||||||
chr16:23375433
|
G | A | 1 | a0001c0003t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1153-305G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375433 | ||||||
chr16:23375503
|
T | C | 2 | a0001c0003t0001g0139a0001c0003t0001g0292 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1153-235T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 7/12 | chr16 | 23375503 | ||||||
chr16:23375938
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1270+83T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23375938 | ||||||
chr16:23375976
|
C | T | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1270+121C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23375976 | ||||||
chr16:23376072
|
G | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(47): Show | 50 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1270+217G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376072 | ||||||
chr16:23376099
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1270+244C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376099 | ||||||
chr16:23376199
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1270+344C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376199 | ||||||
chr16:23376214
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1270+359C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376214 | ||||||
chr16:23376257
|
C | T | 25 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1270+402C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376257 | ||||||
chr16:23376259
|
T | G | 1 | a0001c0011t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1270+404T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376259 | ||||||
chr16:23376326
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1270+471G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376326 | ||||||
chr16:23376345
|
C | CGT | 9 | a0001c0001t0001g0037a0001c0001t0001g0124a0001c0001t0001g0125others(6): Show | 9 | HG02559.hp1 HG03831.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.1270+518_1270+519d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376345 | |||||
chr16:23376345
|
CGT | C | 36 | a0001c0001t0001g0096a0001c0001t0001g0131a0001c0001t0001g0137others(33): Show | 36 | HG00639.hp2 HG01891.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1270+518_1270+519d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376345 | |||||
chr16:23376345
|
CGTGT | C | 7 | a0001c0001t0001g0208a0002c0004t0001g0005a0002c0004t0001g0082others(4): Show | 7 | HG02280.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1270+516_1270+519d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376345 | |||||
chr16:23376345
|
CGTGTGT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0028others(42): Show | 45 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1270+514_1270+519d others(8): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376345 | |||||
chr16:23376345
|
CGTGTGTG others(3): Show |
C | 20 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0019others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1270+510_1270+519d others(12): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376345 | |||||
chr16:23376376
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1270+521A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376376 | ||||||
chr16:23376377
|
C | T | 32 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0064others(29): Show | 32 | HG00639.hp2 HG01891.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1270+522C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376377 | ||||||
chr16:23376556
|
G | T | 2 | a0001c0001t0001g0097a0001c0001t0007g0290 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1271-609G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376556 | ||||||
chr16:23376645
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1271-520C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376645 | ||||||
chr16:23376703
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1271-462A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376703 | ||||||
chr16:23376716
|
C | G | 1 | a0003c0005t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1271-449C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376716 | ||||||
chr16:23376744
|
T | TA | 33 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0251others(30): Show | 33 | HG00639.hp2 HG01123.hp2 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.1271-405dupA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376744 | |||||
chr16:23376744
|
TA | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(27): Show | 30 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1271-405delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 23376744 | |||||
chr16:23376757
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1271-408A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376757 | ||||||
chr16:23376846
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0070others(9): Show | 12 | HG01074.hp1 HG01516.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1271-319C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376846 | ||||||
chr16:23376934
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1271-231G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23376934 | ||||||
chr16:23377088
|
C | T | 12 | a0001c0001t0001g0016a0001c0001t0001g0100a0001c0001t0001g0119others(9): Show | 12 | HG02056.hp2 HG02071.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1271-77C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23377088 | ||||||
chr16:23377094
|
G | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1271-71G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23377094 | ||||||
chr16:23377144
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1271-21G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 8/12 | chr16 | 23377144 | ||||||
chr16:23377574
|
C | CCCTTCCT others(39): Show |
48 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1404+218_1404+219i others(48): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(104): Show |
24 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0035others(21): Show | 24 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1404+218_1404+219i others(113): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(169): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0273 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1404+218_1404+219i others(178): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(234): Show |
1 | a0001c0001t0001g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1404+218_1404+219i others(243): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(81): Show |
1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1404+218_1404+219i others(90): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(16): Show |
130 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(127): Show | 130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1404+195_1404+196i others(25): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(39): Show |
1 | a0001c0001t0001g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1404+195_1404+196i others(48): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377574
|
C | CCCTTCCT others(16): Show |
8 | a0001c0001t0001g0099a0001c0011t0001g0013a0002c0004t0001g0005others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1404+195_1404+196i others(25): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377574 | |||||
chr16:23377581
|
TCCCTCCC others(34): Show |
T | 5 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(2): Show | 5 | HG02145.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1404+196_1404+236d others(43): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377581 | ||||||
chr16:23377582
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0188 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1404+196C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377582 | ||||||
chr16:23377584
|
C | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0188 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1404+198C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377584 | ||||||
chr16:23377586
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0188 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1404+200C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377586 | ||||||
chr16:23377597
|
T | TCCTTCCT others(12): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0188 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1404+218_1404+219i others(21): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377597 | |||||
chr16:23377605
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0121others(5): Show | 8 | HG00544.hp2 HG02027.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1404+219T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377605 | ||||||
chr16:23377607
|
CTTCTTTC others(12): Show |
C | 8 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0121others(5): Show | 8 | HG00544.hp2 HG02027.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1404+225_1404+243d others(21): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377607 | |||||
chr16:23377625
|
CA | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(2): Show | 5 | HG02145.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1404+240delA | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377625 | ||||||
chr16:23377628
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0121others(5): Show | 8 | HG00544.hp2 HG02027.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1404+242T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377628 | ||||||
chr16:23377681
|
TCC | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0269a0001c0001t0001g0271others(2): Show | 5 | HG02145.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1404+297_1404+298d others(4): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377681 | |||||
chr16:23377719
|
CTTCT | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1404+334_1404+337d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377719 | ||||||
chr16:23377723
|
T | C | 14 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0269others(11): Show | 14 | HG00639.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1404+337T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377723 | ||||||
chr16:23377751
|
TTTCTTTC others(32): Show |
T | 45 | a0001c0001t0001g0016a0001c0001t0001g0063a0001c0001t0001g0084others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1404+383_1404+421d others(41): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377751 | |||||
chr16:23377786
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1404+400C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377786 | ||||||
chr16:23377790
|
C | CTTCT | 4 | a0002c0004t0001g0151a0002c0007t0001g0087a0002c0007t0001g0283others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1404+408_1404+411d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377790 | |||||
chr16:23377794
|
T | TTTCC | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0050others(19): Show | 22 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1404+420_1404+423d others(6): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 23377794 | |||||
chr16:23377856
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1404+470A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23377856 | ||||||
chr16:23378104
|
G | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0136a0001c0001t0001g0163 | 3 | NA18955.hp1 NA18995.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1405-602G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378104 | ||||||
chr16:23378163
|
C | A | 1 | a0001c0002t0001g0045 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1405-543C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378163 | ||||||
chr16:23378206
|
C | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0284a0001c0003t0001g0083others(1): Show | 4 | HG02630.hp2 HG03139.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405-500C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378206 | ||||||
chr16:23378247
|
C | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(39): Show | 42 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1405-459C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378247 | ||||||
chr16:23378322
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1405-384T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378322 | ||||||
chr16:23378330
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0143 | 2 | HG02056.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1405-376C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378330 | ||||||
chr16:23378467
|
G | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0279others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-239G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378467 | ||||||
chr16:23378495
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0084others(40): Show | 43 | HG00639.hp2 HG01891.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1405-211A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378495 | ||||||
chr16:23378548
|
T | A | 21 | a0001c0001t0001g0012a0001c0003t0001g0064a0001c0003t0001g0074others(18): Show | 21 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.1405-158T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378548 | ||||||
chr16:23378594
|
C | T | 1 | a0001c0002t0001g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1405-112C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378594 | ||||||
chr16:23378642
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1405-64C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 10/12 | chr16 | 23378642 | ||||||
chr16:23378821
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1466+54C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23378821 | ||||||
chr16:23378880
|
G | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1466+113G>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23378880 | ||||||
chr16:23379016
|
T | TCCTCCAT others(253): Show |
1 | a0001c0001t0001g0084 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1466+312_1466+313i others(262): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379016 | |||||
chr16:23379016
|
T | TCCTCCAT others(123): Show |
2 | a0001c0001t0001g0284a0001c0003t0001g0133 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1466+370_1466+371i others(132): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379016 | |||||
chr16:23379016
|
TCCTCCAT others(77): Show |
T | 1 | a0001c0001t0001g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1466+268_1466+351d others(86): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379016 | |||||
chr16:23379026
|
T | TCCACCCA others(169): Show |
3 | a0001c0001t0001g0279a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG02451.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1466+312_1466+313i others(178): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379026 | |||||
chr16:23379037
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1466+270G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379037 | ||||||
chr16:23379037
|
G | GCCCAGCC others(77): Show |
2 | a0001c0001t0001g0119a0002c0004t0001g0005 | 2 | HG02280.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1466+313_1466+396d others(86): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379037 | |||||
chr16:23379038
|
C | CCCAGCCA others(39): Show |
1 | a0005c0016t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1466+312_1466+313i others(48): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379038 | |||||
chr16:23379054
|
T | TCATTCAT others(253): Show |
1 | a0001c0001t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1466+370_1466+371i others(262): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379054 | |||||
chr16:23379076
|
C | CCCAGCCA others(85): Show |
8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(5): Show | 8 | HG02135.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1466+349_1466+440d others(94): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379076 | |||||
chr16:23379076
|
CCCAGCCA others(85): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1466+349_1466+440d others(94): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379076 | |||||
chr16:23379110
|
T | TCCACCCA others(101): Show |
7 | a0001c0001t0001g0002a0001c0001t0001g0137a0001c0001t0001g0268others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1466+352_1466+459d others(110): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379110 | |||||
chr16:23379119
|
A | ACGCCCAG others(85): Show |
1 | a0001c0001t0007g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1466+353_1466+354i others(94): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379119 | |||||
chr16:23379119
|
A | G | 22 | a0001c0001t0001g0257a0001c0001t0001g0279a0001c0001t0001g0295others(19): Show | 22 | HG00099.hp1 HG02109.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1466+352A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379119 | ||||||
chr16:23379121
|
A | ACCCAGCC others(39): Show |
1 | a0001c0001t0001g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1466+370_1466+371i others(48): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379121 | |||||
chr16:23379121
|
A | ACCCAGCC others(253): Show |
3 | a0002c0007t0001g0087a0002c0007t0001g0283a0002c0007t0001g0294 | 3 | HG01891.hp2 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1466+416_1466+417i others(262): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379121 | |||||
chr16:23379121
|
A | ACCCAGCC others(421): Show |
1 | a0001c0002t0001g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1466+396_1466+397i others(430): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379121 | |||||
chr16:23379121
|
A | ACCCAGCC others(207): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0273 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1466+396_1466+397i others(216): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379121 | |||||
chr16:23379121
|
A | G | 27 | a0001c0001t0001g0101a0001c0001t0001g0257a0001c0001t0001g0276others(24): Show | 27 | HG00099.hp1 HG01891.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1466+354A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379121 | ||||||
chr16:23379146
|
C | CCTCCATT others(55): Show |
1 | a0001c0001t0001g0118 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1466+401_1466+462d others(64): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379146 | |||||
chr16:23379146
|
CCTCCATT others(55): Show |
C | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1466+401_1466+462d others(64): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379146 | |||||
chr16:23379168
|
G | GCCAGCCA others(31): Show |
1 | a0001c0001t0001g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1466+426_1466+427i others(40): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379168 | |||||
chr16:23379168
|
GCCAGCCA others(55): Show |
G | 1 | a0001c0003t0001g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1466+415_1466+476d others(64): Show |
SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 23379168 | |||||
chr16:23379184
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0226a0001c0001t0001g0260 | 3 | HG01123.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1466+417C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379184 | ||||||
chr16:23379230
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1466+463C>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379230 | ||||||
chr16:23379444
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1467-650G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379444 | ||||||
chr16:23379535
|
G | T | 15 | a0001c0001t0001g0049a0001c0001t0001g0098a0001c0001t0001g0104others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1467-559G>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379535 | ||||||
chr16:23379684
|
C | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(4): Show | 7 | HG01167.hp2 HG02258.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1467-410C>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379684 | ||||||
chr16:23379693
|
T | G | 173 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(170): Show | 173 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1467-401T>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379693 | ||||||
chr16:23379753
|
T | C | 1 | a0001c0003t0001g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1467-341T>C | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379753 | ||||||
chr16:23379879
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0251 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1467-215C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23379879 | ||||||
chr16:23380080
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0043others(11): Show | 14 | HG01099.hp2 HG01109.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1467-14G>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 11/12 | chr16 | 23380080 | ||||||
chr16:23380214
|
A | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0299 | 2 | HG01934.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1542+45A>G | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 12/12 | chr16 | 23380214 | ||||||
chr16:23380284
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1542+115T>A | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 12/12 | chr16 | 23380284 | ||||||
chr16:23380309
|
A | T | 72 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0037others(69): Show | 72 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1543-112A>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 12/12 | chr16 | 23380309 | ||||||
chr16:23380404
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1543-17C>T | SCNN1B | ENSG00000168447.11 | transcript | ENST00000343070.7 | protein_coding | 12/12 | chr16 | 23380404 |