Item | Value |
---|---|
geneid | 1183 |
ensemblid | ENSG00000073464.13 |
hgncid | 2022 |
symbol | CLCN4 |
name | chloride voltage-gated channel 4 |
refseq_nuc | NM_001830.4 |
refseq_prot | NP_001821.2 |
ensembl_nuc | ENST00000380833.9 |
ensembl_prot | ENSP00000370213.4 |
mane_status | MANE Select |
chr | chrX |
start | 10156975 |
end | 10237660 |
strand | + |
ver | v1.2 |
region | chrX:10156975-10237660 |
region5000 | chrX:10151975-10242660 |
regionname0 | CLCN4_chrX_10156975_10237660 |
regionname5000 | CLCN4_chrX_10151975_10242660 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 760 | 262 | 72 | 50 | 97 | 13 | 28 | 76 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0002 | 0/0 | 111 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0003 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2283 | 227 | 43 | 45 | 97 | 13 | 27 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0002 | 0/0 | 2283 | 30 | 24 | 5 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0003 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0004 | 0/0 | 2285 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0005 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0006 | 0/0 | 2284 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0007 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
c0008 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4478 | 69 | 1 | 18 | 39 | 3 | 7 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0002 | 0/0 | 4477 | 48 | 20 | 6 | 19 | 1 | 2 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0003 | 0/0 | 4477 | 44 | 0 | 5 | 24 | 2 | 13 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0004 | 1/0 | 4477 | 41 | 20 | 11 | 0 | 7 | 2 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0005 | 0/0 | 4478 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0006 | 0/0 | 4477 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0007 | 0/0 | 4477 | 4 | 0 | 4 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0008 | 0/0 | 4477 | 4 | 3 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0009 | 0/0 | 4477 | 4 | 3 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0010 | 0/0 | 4477 | 3 | 0 | 2 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0011 | 0/0 | 4477 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0012 | 0/0 | 4477 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0013 | 0/0 | 4477 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0014 | 0/0 | 4478 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0015 | 0/0 | 4477 | 2 | 1 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0016 | 0/0 | 4478 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0017 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0018 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0019 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0020 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0021 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0022 | 0/0 | 4478 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0023 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0024 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0025 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0026 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0027 | 0/0 | 4476 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0028 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0029 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0030 | 0/0 | 4478 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0031 | 0/0 | 4478 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0032 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0033 | 0/0 | 4478 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0034 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0035 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0036 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0037 | 0/0 | 4475 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0038 | 0/0 | 4475 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0039 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
t0040 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2283 | 227 | 43 | 45 | 97 | 13 | 27 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0001c0002 | 0/0 | 2283 | 30 | 24 | 5 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0001c0003 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0001c0005 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0001c0007 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0001c0008 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0002c0004 | 0/0 | 2285 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 | |
a0003c0006 | 0/0 | 2284 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6760 | 69 | 1 | 18 | 39 | 3 | 7 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0002 | 0/0 | 6759 | 38 | 13 | 3 | 19 | 1 | 2 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0003 | 0/0 | 6759 | 43 | 0 | 5 | 23 | 2 | 13 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0004 | 1/0 | 6759 | 27 | 8 | 9 | 0 | 7 | 2 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0005 | 0/0 | 6760 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0006 | 0/0 | 6759 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0007 | 0/0 | 6759 | 4 | 0 | 4 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0008 | 0/0 | 6759 | 4 | 3 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0009 | 0/0 | 6759 | 3 | 2 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0010 | 0/0 | 6759 | 3 | 0 | 2 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0011 | 0/0 | 6759 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0012 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0013 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0014 | 0/0 | 6760 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0015 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0017 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0019 | 0/0 | 6759 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0020 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0021 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0022 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0023 | 0/0 | 6759 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0024 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0025 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0028 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0029 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0030 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0031 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0032 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0033 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0034 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0035 | 0/0 | 6762 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0036 | 0/0 | 6759 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0001t0040 | 0/0 | 6759 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0002 | 0/0 | 6759 | 8 | 5 | 3 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0004 | 0/0 | 6759 | 14 | 12 | 2 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0009 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0013 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0015 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0018 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0026 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0037 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0038 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0002t0039 | 0/0 | 6759 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0003t0016 | 0/0 | 6760 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0005t0002 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0007t0012 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0001c0008t0002 | 0/0 | 6759 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0002c0004t0003 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
a0003c0006t0027 | 0/0 | 6759 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | copy fasta | chrX | 10151975 | 10242660 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0008g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0014g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0015g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0017g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0019g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0020g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0021g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0022g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0023g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0024g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0025g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0028g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0029g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0030g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0031g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0032g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0033g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0034g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0035g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0036g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0001t0040g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0038g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0002t0039g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0003t0016g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0003t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0005t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0007t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0001c0008t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0002c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
a0003c0006t0027g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0080 | EUR | GBR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0112 | EUR | GBR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0194 | EUR | FIN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | FIN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0190 | EUR | FIN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00597 | hp2 | a0001 | c0001 | t0028 | g0090 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00609 | hp1 | a0001 | c0001 | t0021 | g0245 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01074 | hp1 | a0001 | c0002 | t0004 | g0050 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01106 | hp1 | a0001 | c0002 | t0004 | g0036 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0141 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0142 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01192 | hp1 | a0001 | c0001 | t0019 | g0261 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0078 | AMR | PUR | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01255 | hp1 | a0001 | c0001 | t0010 | g0169 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0168 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01346 | hp2 | a0001 | c0001 | t0040 | g0156 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0092 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0093 | EUR | IBS | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01884 | hp1 | a0001 | c0002 | t0037 | g0032 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0145 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02015 | hp1 | a0001 | c0001 | t0011 | g0243 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0077 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02129 | hp1 | a0001 | c0001 | t0025 | g0129 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CDX | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CDX | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02258 | hp1 | a0001 | c0005 | t0002 | g0100 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02293 | hp1 | a0001 | c0001 | t0007 | g0107 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0056 | AMR | PEL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02451 | hp1 | a0001 | c0002 | t0038 | g0033 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02572 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02602 | hp1 | a0001 | c0002 | t0039 | g0155 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02615 | hp2 | a0001 | c0002 | t0004 | g0134 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02622 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02630 | hp1 | a0001 | c0008 | t0002 | g0099 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0046 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02683 | hp1 | a0001 | c0001 | t0023 | g0122 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0131 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02818 | hp1 | a0001 | c0002 | t0004 | g0106 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0098 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02922 | hp1 | a0001 | c0001 | t0017 | g0057 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0047 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02970 | hp2 | a0001 | c0007 | t0012 | g0101 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02976 | hp1 | a0001 | c0001 | t0032 | g0067 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0049 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03195 | hp1 | a0001 | c0002 | t0009 | g0075 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0084 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0136 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03486 | hp1 | a0001 | c0002 | t0013 | g0035 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03516 | hp2 | a0001 | c0003 | t0016 | g0086 | AFR | ESN | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03669 | hp2 | a0001 | c0001 | t0036 | g0017 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG04184 | hp2 | a0001 | c0001 | t0010 | g0059 | SAS | BEB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18522 | hp1 | a0001 | c0002 | t0018 | g0042 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | CHB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | CHB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18906 | hp1 | a0001 | c0001 | t0034 | g0073 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18906 | hp2 | a0001 | c0002 | t0004 | g0045 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18940 | hp1 | a0001 | c0001 | t0022 | g0118 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18942 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18961 | hp1 | a0001 | c0001 | t0014 | g0005 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18970 | hp1 | a0001 | c0001 | t0030 | g0255 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18974 | hp1 | a0002 | c0004 | t0003 | g0196 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18983 | hp1 | a0001 | c0001 | t0033 | g0216 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18997 | hp1 | a0001 | c0001 | t0035 | g0231 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19006 | hp1 | a0001 | c0001 | t0020 | g0173 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19010 | hp1 | a0001 | c0001 | t0011 | g0247 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19060 | hp2 | a0001 | c0001 | t0011 | g0181 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19072 | hp1 | a0003 | c0006 | t0027 | g0248 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19080 | hp1 | a0001 | c0001 | t0024 | g0209 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19086 | hp1 | a0001 | c0001 | t0015 | g0203 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19088 | hp1 | a0001 | c0001 | t0031 | g0241 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19240 | hp1 | a0001 | c0003 | t0016 | g0087 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ASW | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0147 | AFR | ASW | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0116 | EUR | TSI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0262 | EUR | TSI | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | GIH | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02109 | hp2 | a0001 | c0002 | t0026 | g0034 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0053 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA20300 | hp2 | a0001 | c0002 | t0015 | g0030 | AFR | USA | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA21309 | hp1 | a0001 | c0002 | t0004 | g0085 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | LWK | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0089 | REF | REF | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0114 | REF | REF | CLCN4_chrX_10151975_10242660 | CLCN4 | chrX | 10151975 | 10242660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:10194993 | T | TA | 1 | a0002 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.328dupA | p.Ser110fs | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/13 | 729/6759 | 329/2283 | 110/760 | INFO_REALIGN_3_PRIME | chrX | 10194993 | |
chrX:10195054 | C | CT | 1 | a0002 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.388_389insT | p.Pro130fs | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/13 | 789/6759 | 389/2283 | 130/760 | chrX | 10195054 | ||
chrX:10214005 | T | TC | 1 | a0003 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.1905dupC | p.Val636fs | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/13 | 2306/6759 | 1906/2283 | 636/760 | INFO_REALIGN_3_PRIME | chrX | 10214005 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:10208176 | G | A | 1 | a0001c0003 | 2 | HG03516.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.975G>A | p.Thr325Thr | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/13 | 1375/6759 | 975/2283 | 325/760 | chrX | 10208176 | ||
chrX:10212514 | G | A | 2 | a0001c0002a0001c0005 | 31 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(28): Show |
synonymous_variant | LOW | c.1437G>A | p.Ala479Ala | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/13 | 1837/6759 | 1437/2283 | 479/760 | chrX | 10212514 | ||
chrX:10220716 | G | A | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2031G>A | p.Thr677Thr | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/13 | 2431/6759 | 2031/2283 | 677/760 | chrX | 10220716 | ||
chrX:10220869 | G | A | 2 | a0001c0005a0001c0008 | 2 | HG02258.hp1 HG02630.hp1 |
synonymous_variant | LOW | c.2184G>A | p.Thr728Thr | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/13 | 2584/6759 | 2184/2283 | 728/760 | chrX | 10220869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:10158391 | C | T | 2 | a0001c0001t0040a0001c0002t0039 | 2 | HG01346.hp2 HG02602.hp1 |
5_prime_UTR_variant | MODIFIER | c.-172C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26642 | chrX | 10158391 | |||||
chrX:10158392 | C | A | 1 | a0001c0001t0017 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26641 | chrX | 10158392 | |||||
chrX:10158394 | C | G | 1 | a0001c0003t0016 | 2 | HG03516.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-169C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26639 | chrX | 10158394 | |||||
chrX:10158419 | C | T | 2 | a0001c0002t0037a0001c0002t0038 | 2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-144C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26614 | chrX | 10158419 | |||||
chrX:10158421 | CGA | C | 2 | a0001c0002t0037a0001c0002t0038 | 2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-140_-139delAG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26609 | INFO_REALIGN_3_PRIME | chrX | 10158421 | ||||
chrX:10158424 | G | C | 2 | a0001c0002t0037a0001c0002t0038 | 2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-139G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26609 | chrX | 10158424 | |||||
chrX:10158425 | G | T | 2 | a0001c0002t0037a0001c0002t0038 | 2 | HG01884.hp1 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-138G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/13 | 26608 | chrX | 10158425 | |||||
chrX:10233677 | T | C | 2 | a0001c0001t0010a0001c0002t0039 | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 93 | chrX | 10233677 | |||||
chrX:10233740 | A | G | 31 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(28): Show | 160 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*156A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 156 | chrX | 10233740 | |||||
chrX:10233783 | C | T | 1 | a0001c0001t0036 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 199 | chrX | 10233783 | |||||
chrX:10234167 | G | GT | 1 | a0001c0001t0035 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 586 | INFO_REALIGN_3_PRIME | chrX | 10234167 | ||||
chrX:10234303 | C | T | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(26): Show | 158 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*719C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 719 | chrX | 10234303 | |||||
chrX:10234708 | G | T | 11 | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(8): Show | 58 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1124 | chrX | 10234708 | |||||
chrX:10234796 | C | G | 1 | a0001c0001t0034 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1212 | chrX | 10234796 | |||||
chrX:10234814 | C | T | 1 | a0001c0001t0033 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1230 | chrX | 10234814 | |||||
chrX:10234891 | C | T | 1 | a0001c0002t0038 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1307 | chrX | 10234891 | |||||
chrX:10235148 | G | A | 14 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(11): Show | 66 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1564G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1564 | chrX | 10235148 | |||||
chrX:10235148 | G | GT | 1 | a0001c0001t0035 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1569dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1570 | INFO_REALIGN_3_PRIME | chrX | 10235148 | ||||
chrX:10235302 | G | A | 1 | a0001c0001t0007 | 4 | HG01168.hp2 HG01169.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1718G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1718 | chrX | 10235302 | |||||
chrX:10235308 | C | T | 2 | a0001c0001t0006a0001c0001t0032 | 6 | HG02615.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1724C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1724 | chrX | 10235308 | |||||
chrX:10235355 | A | C | 18 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(15): Show | 101 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1771A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1771 | chrX | 10235355 | |||||
chrX:10235487 | T | C | 2 | a0001c0001t0010a0001c0002t0039 | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1903T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 1903 | chrX | 10235487 | |||||
chrX:10235681 | G | A | 1 | a0001c0001t0025 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2097 | chrX | 10235681 | |||||
chrX:10235691 | C | T | 1 | a0001c0001t0031 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2107C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2107 | chrX | 10235691 | |||||
chrX:10235896 | T | C | 2 | a0001c0001t0005a0001c0003t0016 | 7 | HG02809.hp2 HG03139.hp1 HG03516.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2312T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2312 | chrX | 10235896 | |||||
chrX:10236210 | G | A | 1 | a0001c0001t0011 | 3 | HG02015.hp1 NA19010.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2626G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2626 | chrX | 10236210 | |||||
chrX:10236227 | T | A | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(30): Show | 165 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*2643T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2643 | chrX | 10236227 | |||||
chrX:10236232 | C | A | 1 | a0001c0001t0020 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2648C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2648 | chrX | 10236232 | |||||
chrX:10236262 | TG | T | 1 | a0003c0006t0027 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2681delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 2681 | INFO_REALIGN_3_PRIME | chrX | 10236262 | ||||
chrX:10236591 | T | A | 1 | a0001c0001t0021 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3007T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3007 | chrX | 10236591 | |||||
chrX:10236669 | A | G | 1 | a0001c0001t0019 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3085A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3085 | chrX | 10236669 | |||||
chrX:10236723 | G | GT | 1 | a0001c0001t0022 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3152dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3153 | INFO_REALIGN_3_PRIME | chrX | 10236723 | ||||
chrX:10236772 | A | G | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(13): Show | 97 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3188A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3188 | chrX | 10236772 | |||||
chrX:10236835 | G | C | 1 | a0001c0001t0014 | 2 | NA18942.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3251G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3251 | chrX | 10236835 | |||||
chrX:10236983 | A | G | 2 | a0001c0001t0010a0001c0002t0039 | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3399A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3399 | chrX | 10236983 | |||||
chrX:10236988 | GC | G | 1 | a0001c0001t0028 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3405delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3405 | chrX | 10236988 | |||||
chrX:10237436 | G | A | 1 | a0001c0001t0030 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3852G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3852 | chrX | 10237436 | |||||
chrX:10237541 | C | A | 12 | a0001c0001t0002a0001c0001t0007a0001c0001t0020others(9): Show | 59 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3957C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3957 | chrX | 10237541 | |||||
chrX:10237548 | G | GT | 9 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(6): Show | 83 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3973dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 13/13 | 3974 | INFO_REALIGN_3_PRIME | chrX | 10237548 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:10157125 | A | G | 4 | a0001c0001t0002g0260a0001c0001t0004g0262a0001c0001t0004g0263others(1): Show | 4 | HG01081.hp2 HG01192.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-275+25A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157125 | ||||||
chrX:10157233 | C | T | 105 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-275+133C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157233 | ||||||
chrX:10157362 | G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-275+262G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157362 | ||||||
chrX:10157394 | C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(48): Show | 52 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-275+294C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157394 | ||||||
chrX:10157520 | A | G | 2 | a0001c0001t0001g0154a0001c0001t0003g0153 | 2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-275+420A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157520 | ||||||
chrX:10157530 | T | C | 6 | a0001c0001t0004g0054a0001c0001t0008g0055a0001c0001t0008g0056others(3): Show | 6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-275+430T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157530 | ||||||
chrX:10157939 | G | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(50): Show | 54 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-274-350G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10157939 | ||||||
chrX:10158030 | C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(48): Show | 52 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-274-259C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158030 | ||||||
chrX:10158063 | G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(48): Show | 52 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.-274-226G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158063 | ||||||
chrX:10158088 | G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(2): Show | 5 | HG01081.hp1 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-274-201G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158088 | ||||||
chrX:10158217 | T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-274-72T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 1/12 | chrX | 10158217 | ||||||
chrX:10158588 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-12+37G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10158588 | ||||||
chrX:10158588 | GC | G | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12+42delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10158588 | |||||
chrX:10158673 | T | C | 1 | a0001c0001t0003g0157 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-12+122T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10158673 | ||||||
chrX:10159086 | T | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(26): Show | 30 | HG01070.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12+535T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159086 | ||||||
chrX:10159132 | A | AT | 2 | a0001c0001t0001g0257a0001c0001t0004g0258 | 2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+591dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10159132 | |||||
chrX:10159132 | AT | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 49 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-12+591delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10159132 | |||||
chrX:10159155 | T | A | 2 | a0001c0001t0005g0060a0001c0001t0006g0062 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-12+604T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159155 | ||||||
chrX:10159217 | T | G | 2 | a0001c0002t0002g0029a0001c0002t0015g0030 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-12+666T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159217 | ||||||
chrX:10159426 | G | C | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+875G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159426 | ||||||
chrX:10159597 | T | C | 1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+1046T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159597 | ||||||
chrX:10159637 | TA | T | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12+1089delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10159637 | |||||
chrX:10159705 | G | GT | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12+1156dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10159705 | |||||
chrX:10159779 | TC | T | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12+1232delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10159779 | |||||
chrX:10159810 | G | C | 1 | a0001c0001t0006g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-12+1259G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159810 | ||||||
chrX:10159845 | G | A | 1 | a0001c0001t0004g0069 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-12+1294G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10159845 | ||||||
chrX:10160159 | G | C | 2 | a0001c0001t0003g0071a0001c0001t0004g0070 | 2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-12+1608G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160159 | ||||||
chrX:10160539 | A | G | 5 | a0001c0001t0004g0051a0001c0002t0004g0046a0001c0002t0004g0048others(2): Show | 5 | HG01074.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1988A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160539 | ||||||
chrX:10160665 | G | A | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+2114G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160665 | ||||||
chrX:10160727 | C | T | 6 | a0001c0001t0002g0152a0001c0001t0004g0148a0001c0001t0004g0151others(3): Show | 6 | HG01109.hp1 HG02559.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+2176C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160727 | ||||||
chrX:10160748 | A | G | 109 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(106): Show | 109 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-12+2197A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160748 | ||||||
chrX:10160873 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-12+2322T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160873 | ||||||
chrX:10160911 | C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(43): Show | 47 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+2360C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160911 | ||||||
chrX:10160937 | C | A | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+2386C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160937 | ||||||
chrX:10160939 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-12+2388G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10160939 | ||||||
chrX:10160985 | A | AG | 1 | a0001c0001t0001g0259 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12+2441dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10160985 | |||||
chrX:10161029 | G | A | 1 | a0001c0001t0003g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-12+2478G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161029 | ||||||
chrX:10161124 | G | GCT | 28 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(25): Show | 28 | HG00597.hp2 HG01346.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.-12+2610_-12+2611d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCT | 22 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0242others(19): Show | 22 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-12+2608_-12+2611d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCT | 10 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02027.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+2606_-12+2611d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(1): Show |
50 | a0001c0001t0001g0188a0001c0001t0001g0197a0001c0001t0001g0199others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-12+2604_-12+2611d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(3): Show |
22 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0179others(19): Show | 22 | HG00438.hp2 HG00597.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-12+2602_-12+2611d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(5): Show |
12 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0002g0161others(9): Show | 12 | HG00323.hp1 HG00438.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+2600_-12+2611d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(7): Show |
3 | a0001c0001t0003g0160a0001c0001t0004g0054a0001c0002t0004g0049 | 3 | HG02976.hp2 NA18948.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-12+2598_-12+2611d others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(9): Show |
2 | a0001c0002t0004g0046a0001c0002t0004g0048 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-12+2596_-12+2611d others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(11): Show |
1 | a0001c0002t0002g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+2594_-12+2611d others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | G | GCTCTCTC others(13): Show |
1 | a0001c0002t0002g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-12+2592_-12+2611d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | GCT | G | 9 | a0001c0001t0002g0066a0001c0001t0002g0260a0001c0001t0005g0143others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+2610_-12+2611d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | GCTCT | G | 11 | a0001c0001t0001g0144a0001c0001t0002g0152a0001c0001t0004g0148others(8): Show | 11 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+2608_-12+2611d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | GCTCTCT | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0146others(1): Show | 4 | HG02723.hp1 NA18970.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+2606_-12+2611d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161124 | GCTCTCTC others(3): Show |
G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(44): Show | 48 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12+2602_-12+2611d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161124 | |||||
chrX:10161334 | C | T | 11 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0008g0037others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+2783C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161334 | ||||||
chrX:10161440 | G | T | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12+2889G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161440 | ||||||
chrX:10161532 | C | T | 6 | a0001c0001t0002g0152a0001c0001t0004g0148a0001c0001t0004g0151others(3): Show | 6 | HG01109.hp1 HG02559.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+2981C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161532 | ||||||
chrX:10161533 | G | A | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+2982G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161533 | ||||||
chrX:10161549 | T | TA | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+3000dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161549 | |||||
chrX:10161657 | G | A | 102 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+3106G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161657 | ||||||
chrX:10161780 | T | TG | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+3234dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10161780 | |||||
chrX:10161794 | T | C | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-12+3243T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161794 | ||||||
chrX:10161796 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-12+3245C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161796 | ||||||
chrX:10161827 | G | A | 1 | a0001c0001t0006g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-12+3276G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10161827 | ||||||
chrX:10162013 | C | CT | 9 | a0001c0001t0002g0260a0001c0001t0003g0071a0001c0001t0003g0104others(6): Show | 9 | HG00639.hp1 HG01256.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+3484dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | |||||
chrX:10162013 | CT | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(55): Show | 59 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.-12+3484delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | |||||
chrX:10162013 | CTT | C | 89 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(86): Show | 89 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-12+3483_-12+3484d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | |||||
chrX:10162013 | CTTT | C | 4 | a0001c0001t0001g0188a0001c0001t0003g0167a0001c0001t0003g0189others(1): Show | 4 | HG00639.hp2 HG03704.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+3482_-12+3484d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162013 | |||||
chrX:10162064 | C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 49 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-12+3513C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162064 | ||||||
chrX:10162074 | G | GT | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+3524dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162074 | |||||
chrX:10162078 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12+3527T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162078 | ||||||
chrX:10162079 | AG | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12+3529delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162079 | ||||||
chrX:10162111 | T | G | 2 | a0001c0003t0016g0086a0001c0003t0016g0087 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-12+3560T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162111 | ||||||
chrX:10162121 | C | T | 6 | a0001c0001t0004g0054a0001c0001t0008g0055a0001c0001t0008g0056others(3): Show | 6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+3570C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162121 | ||||||
chrX:10162168 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-12+3617G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162168 | ||||||
chrX:10162310 | C | T | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-12+3759C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162310 | ||||||
chrX:10162319 | G | A | 3 | a0001c0001t0004g0190a0001c0001t0010g0168a0001c0001t0010g0169 | 3 | HG00323.hp2 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-12+3768G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162319 | ||||||
chrX:10162765 | G | GT | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+4219dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10162765 | |||||
chrX:10162913 | C | T | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+4362C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162913 | ||||||
chrX:10162979 | G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(166): Show | 170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-12+4428G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10162979 | ||||||
chrX:10163118 | T | C | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+4567T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163118 | ||||||
chrX:10163138 | C | CT | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+4590dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163138 | |||||
chrX:10163242 | TG | T | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-12+4696delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163242 | |||||
chrX:10163363 | A | AT | 8 | a0001c0001t0001g0236a0001c0001t0004g0051a0001c0001t0040g0156others(5): Show | 8 | HG01074.hp1 HG01346.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+4825dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163363 | |||||
chrX:10163363 | A | ATT | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(43): Show | 47 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+4824_-12+4825d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163363 | |||||
chrX:10163363 | A | ATTT | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12+4823_-12+4825d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163363 | |||||
chrX:10163375 | T | TTG | 1 | a0001c0001t0001g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+4827_-12+4828d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163375 | |||||
chrX:10163410 | TTTTC | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(43): Show | 47 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+4863_-12+4866d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163410 | |||||
chrX:10163411 | TTTC | T | 2 | a0001c0002t0004g0031a0001c0002t0015g0030 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12+4863_-12+4865d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163411 | |||||
chrX:10163414 | C | CCT | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+4863_-12+4864i others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163414 | ||||||
chrX:10163414 | CT | C | 2 | a0001c0001t0009g0061a0003c0006t0027g0248 | 2 | HG02965.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-12+4874delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163414 | |||||
chrX:10163455 | C | T | 1 | a0001c0001t0003g0224 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-12+4904C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163455 | ||||||
chrX:10163563 | C | T | 17 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(14): Show | 17 | HG02135.hp1 HG03710.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+5012C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163563 | ||||||
chrX:10163628 | A | G | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+5077A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163628 | ||||||
chrX:10163640 | A | AGGGGATG | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+5090_-12+5096d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163640 | |||||
chrX:10163657 | C | T | 8 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0236others(5): Show | 8 | NA18970.hp1 NA18981.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+5106C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163657 | ||||||
chrX:10163702 | G | A | 1 | a0001c0002t0004g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-12+5151G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163702 | ||||||
chrX:10163884 | A | AC | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+5337dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10163884 | |||||
chrX:10163981 | T | G | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12+5430T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10163981 | ||||||
chrX:10164031 | C | CT | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+5480_-12+5481i others(3): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164031 | ||||||
chrX:10164101 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12+5550G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164101 | ||||||
chrX:10164127 | C | T | 1 | a0001c0001t0030g0255 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-12+5576C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164127 | ||||||
chrX:10164210 | T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 49 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-12+5659T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164210 | ||||||
chrX:10164345 | T | TG | 1 | a0001c0001t0002g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-12+5798dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10164345 | |||||
chrX:10164528 | GA | G | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-12+5980delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10164528 | |||||
chrX:10164784 | G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(26): Show | 30 | HG01070.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12+6233G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164784 | ||||||
chrX:10164942 | C | T | 1 | a0001c0001t0004g0138 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-12+6391C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10164942 | ||||||
chrX:10165010 | C | T | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+6459C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165010 | ||||||
chrX:10165026 | CT | C | 1 | a0001c0002t0004g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12+6477delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10165026 | |||||
chrX:10165032 | G | GC | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+6483dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10165032 | |||||
chrX:10165085 | C | T | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0005t0002g0100others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+6534C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165085 | ||||||
chrX:10165104 | A | G | 102 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+6553A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165104 | ||||||
chrX:10165189 | G | A | 2 | a0001c0001t0003g0159a0001c0001t0003g0170 | 2 | NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-12+6638G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165189 | ||||||
chrX:10165213 | A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(2): Show | 5 | HG01081.hp1 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6662A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165213 | ||||||
chrX:10165309 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-12+6758C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165309 | ||||||
chrX:10165377 | C | T | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-12+6826C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165377 | ||||||
chrX:10165448 | C | T | 1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12+6897C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165448 | ||||||
chrX:10165677 | T | TG | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+7129dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10165677 | |||||
chrX:10165687 | T | TG | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+7138dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10165687 | |||||
chrX:10165712 | GC | G | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-12+7164delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10165712 | |||||
chrX:10165717 | C | G | 2 | a0001c0001t0001g0257a0001c0001t0004g0258 | 2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+7166C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10165717 | ||||||
chrX:10166361 | C | T | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12+7810C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166361 | ||||||
chrX:10166493 | A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(44): Show | 48 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12+7942A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166493 | ||||||
chrX:10166872 | G | A | 2 | a0001c0002t0037g0032a0001c0002t0038g0033 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-12+8321G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166872 | ||||||
chrX:10166899 | A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-12+8348A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166899 | ||||||
chrX:10166909 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-12+8358C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10166909 | ||||||
chrX:10167042 | G | C | 2 | a0001c0001t0001g0257a0001c0001t0004g0258 | 2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+8491G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167042 | ||||||
chrX:10167121 | G | A | 6 | a0001c0001t0004g0054a0001c0001t0008g0055a0001c0001t0008g0056others(3): Show | 6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+8570G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167121 | ||||||
chrX:10167148 | T | G | 1 | a0001c0001t0003g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-12+8597T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167148 | ||||||
chrX:10167237 | G | T | 1 | a0001c0001t0004g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-12+8686G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167237 | ||||||
chrX:10167325 | C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-12+8774C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167325 | ||||||
chrX:10167409 | A | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00597.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-12+8858A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167409 | ||||||
chrX:10167702 | C | T | 6 | a0001c0001t0004g0054a0001c0001t0008g0055a0001c0001t0008g0056others(3): Show | 6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+9151C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167702 | ||||||
chrX:10167818 | G | C | 1 | a0001c0001t0007g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12+9267G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10167818 | ||||||
chrX:10168084 | T | C | 10 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+9533T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168084 | ||||||
chrX:10168277 | A | T | 3 | a0001c0001t0009g0078a0001c0001t0034g0073a0001c0002t0004g0045 | 3 | HG01243.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12+9726A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168277 | ||||||
chrX:10168284 | A | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00597.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-12+9733A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168284 | ||||||
chrX:10168588 | C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(57): Show | 61 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-12+10037C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168588 | ||||||
chrX:10168621 | T | C | 1 | a0001c0001t0004g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-12+10070T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168621 | ||||||
chrX:10168662 | A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-12+10111A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168662 | ||||||
chrX:10168800 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-12+10249C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168800 | ||||||
chrX:10168805 | C | T | 3 | a0001c0001t0002g0130a0001c0001t0006g0062a0001c0002t0009g0075 | 3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+10254C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10168805 | ||||||
chrX:10169123 | A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(65): Show | 69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10572A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169123 | ||||||
chrX:10169321 | A | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(65): Show | 69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10770A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169321 | ||||||
chrX:10169345 | C | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(57): Show | 61 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-12+10794C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169345 | ||||||
chrX:10169364 | G | T | 7 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0135others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+10813G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169364 | ||||||
chrX:10169483 | A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(65): Show | 69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10932A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169483 | ||||||
chrX:10169500 | AAAAC | A | 5 | a0001c0001t0002g0146a0001c0002t0004g0046a0001c0002t0004g0048others(2): Show | 5 | HG01074.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+10969_-12+1097 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169500 | |||||
chrX:10169516 | C | A | 14 | a0001c0001t0002g0066a0001c0001t0004g0054a0001c0001t0006g0063others(11): Show | 14 | HG01346.hp2 HG01884.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+10965C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169516 | ||||||
chrX:10169520 | C | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(65): Show | 69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+10969C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169520 | ||||||
chrX:10169667 | G | A | 4 | a0001c0002t0002g0039a0001c0002t0002g0040a0001c0002t0002g0041others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+11116G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169667 | ||||||
chrX:10169765 | C | CT | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-12+11223dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169765 | |||||
chrX:10169775 | CTTTTTCT others(11): Show |
C | 1 | a0001c0001t0006g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12+11230_-12+1124 others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169775 | |||||
chrX:10169776 | TTTTTC | T | 1 | a0001c0001t0025g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-12+11240_-12+1124 others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169776 | |||||
chrX:10169776 | TTTTTCTT others(3): Show |
T | 4 | a0001c0001t0003g0011a0001c0002t0004g0046a0001c0002t0004g0049others(1): Show | 4 | HG01074.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+11235_-12+1124 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169776 | |||||
chrX:10169777 | TTTTCTTT others(2): Show |
T | 1 | a0001c0002t0004g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+11230_-12+1123 others(13): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169777 | |||||
chrX:10169779 | TTCTTTTC others(5): Show |
T | 1 | a0001c0001t0001g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-12+11230_-12+1124 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169779 | |||||
chrX:10169780 | TCTTTTCT others(4): Show |
T | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(50): Show | 54 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+11230_-12+1124 others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169780 | ||||||
chrX:10169789 | T | TC | 1 | a0001c0001t0004g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-12+11238_-12+1123 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169789 | ||||||
chrX:10169790 | T | C | 7 | a0001c0001t0008g0055a0001c0001t0008g0056a0001c0001t0017g0057others(4): Show | 7 | HG01346.hp2 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+11239T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169790 | ||||||
chrX:10169791 | C | CT | 16 | a0001c0001t0001g0091a0001c0001t0002g0130a0001c0001t0002g0146others(13): Show | 16 | HG01516.hp2 HG01517.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12+11255dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169791 | |||||
chrX:10169791 | C | T | 13 | a0001c0001t0003g0011a0001c0001t0004g0054a0001c0001t0008g0055others(10): Show | 13 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+11240C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169791 | ||||||
chrX:10169810 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-12+11259A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169810 | ||||||
chrX:10169816 | TCTCG | T | 2 | a0001c0001t0002g0166a0001c0001t0003g0160 | 2 | NA18948.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-12+11269_-12+1127 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10169816 | |||||
chrX:10169898 | C | G | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | NA18967.hp1 NA18984.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-12+11347C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169898 | ||||||
chrX:10169934 | A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(65): Show | 69 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.-12+11383A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10169934 | ||||||
chrX:10170330 | A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-12+11779A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170330 | ||||||
chrX:10170357 | C | T | 6 | a0001c0001t0004g0054a0001c0001t0008g0055a0001c0001t0008g0056others(3): Show | 6 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+11806C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170357 | ||||||
chrX:10170505 | G | C | 3 | a0001c0001t0004g0080a0001c0001t0004g0109a0001c0002t0002g0081 | 3 | HG00099.hp1 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-12+11954G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170505 | ||||||
chrX:10170537 | G | T | 1 | a0001c0001t0002g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-12+11986G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170537 | ||||||
chrX:10170704 | C | T | 1 | a0001c0001t0017g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+12153C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170704 | ||||||
chrX:10170733 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12+12182C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170733 | ||||||
chrX:10170758 | C | A | 5 | a0001c0001t0002g0066a0001c0001t0006g0064a0001c0001t0006g0065others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+12207C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170758 | ||||||
chrX:10170758 | C | T | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-12+12207C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10170758 | ||||||
chrX:10171517 | C | T | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+12966C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10171517 | ||||||
chrX:10171609 | A | G | 5 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | NA18944.hp1 NA18981.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+13058A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10171609 | ||||||
chrX:10171992 | A | G | 3 | a0001c0001t0009g0078a0001c0001t0034g0073a0001c0002t0004g0045 | 3 | HG01243.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11-13030A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10171992 | ||||||
chrX:10172296 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-11-12726C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172296 | ||||||
chrX:10172639 | G | T | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11-12383G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172639 | ||||||
chrX:10172684 | C | CGT | 110 | a0001c0001t0001g0123a0001c0001t0001g0162a0001c0001t0001g0163others(107): Show | 110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-11-12322_-11-1232 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10172684 | |||||
chrX:10172684 | C | CGTGT | 7 | a0001c0001t0003g0165a0001c0001t0004g0054a0001c0001t0008g0055others(4): Show | 7 | HG01884.hp2 HG02293.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-12324_-11-1232 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10172684 | |||||
chrX:10172691 | G | GTC | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(57): Show | 61 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.-11-12330_-11-1232 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10172691 | |||||
chrX:10172734 | A | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.-11-12288A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172734 | ||||||
chrX:10172772 | TG | T | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11-12249delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10172772 | ||||||
chrX:10173244 | C | T | 4 | a0001c0002t0004g0046a0001c0002t0004g0048a0001c0002t0004g0049others(1): Show | 4 | HG01074.hp1 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11778C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173244 | ||||||
chrX:10173263 | G | A | 7 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0135others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-11759G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173263 | ||||||
chrX:10173317 | C | G | 1 | a0001c0001t0024g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-11-11705C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173317 | ||||||
chrX:10173328 | C | G | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-11-11694C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173328 | ||||||
chrX:10173333 | C | T | 1 | a0001c0001t0023g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-11-11689C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173333 | ||||||
chrX:10173351 | TG | T | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11-11667delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10173351 | |||||
chrX:10173375 | G | A | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11-11647G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173375 | ||||||
chrX:10173383 | G | A | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-11639G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173383 | ||||||
chrX:10173400 | G | A | 3 | a0001c0001t0002g0130a0001c0001t0006g0062a0001c0002t0009g0075 | 3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-11622G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173400 | ||||||
chrX:10173460 | G | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(54): Show | 58 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11-11562G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173460 | ||||||
chrX:10173735 | C | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(54): Show | 58 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11-11287C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173735 | ||||||
chrX:10173847 | C | G | 102 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-11-11175C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10173847 | ||||||
chrX:10174105 | C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-10917C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174105 | ||||||
chrX:10174188 | G | GA | 1 | a0001c0001t0002g0105 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11-10834_-11-1083 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174188 | ||||||
chrX:10174208 | TC | T | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11-10809delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10174208 | |||||
chrX:10174211 | C | T | 110 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(107): Show | 110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-11-10811C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174211 | ||||||
chrX:10174212 | C | T | 7 | a0001c0001t0002g0152a0001c0001t0004g0148a0001c0001t0004g0151others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-10810C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174212 | ||||||
chrX:10174376 | T | G | 111 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-11-10646T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174376 | ||||||
chrX:10174420 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-11-10602C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174420 | ||||||
chrX:10174532 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-10490G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174532 | ||||||
chrX:10174601 | G | C | 2 | a0001c0001t0010g0168a0001c0001t0010g0169 | 2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-11-10421G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174601 | ||||||
chrX:10174728 | C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(47): Show | 51 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.-11-10294C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174728 | ||||||
chrX:10174841 | C | A | 1 | a0001c0001t0004g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11-10181C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174841 | ||||||
chrX:10174965 | A | G | 103 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-11-10057A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10174965 | ||||||
chrX:10175060 | G | A | 2 | a0001c0001t0001g0001a0001c0001t0010g0059 | 3 | HG01515.hp1 HG01517.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-11-9962G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175060 | ||||||
chrX:10175175 | G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(56): Show | 60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-9847G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175175 | ||||||
chrX:10175357 | T | TTGGACCA others(8): Show |
4 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-9662_-11-9648d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175357 | |||||
chrX:10175404 | G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11-9618G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175404 | ||||||
chrX:10175443 | G | GGCAGCCA | 1 | a0001c0001t0002g0250 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-11-9564_-11-9558d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175443 | |||||
chrX:10175444 | GCAGCCAG others(5): Show |
G | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-9577_-11-9566d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175444 | ||||||
chrX:10175490 | A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(180): Show | 184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-11-9532A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175490 | ||||||
chrX:10175681 | A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(180): Show | 184 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-11-9341A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175681 | ||||||
chrX:10175691 | TG | T | 1 | a0001c0001t0002g0105 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11-9329delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175691 | |||||
chrX:10175744 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-11-9278C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175744 | ||||||
chrX:10175855 | C | CCT | 7 | a0001c0001t0005g0060a0001c0001t0005g0143a0001c0001t0009g0061others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-9151_-11-9150d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175855 | |||||
chrX:10175857 | T | C | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-11-9165T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175857 | ||||||
chrX:10175917 | T | TCTCTCTC others(15): Show |
6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-9099_-11-9078d others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175917 | |||||
chrX:10175941 | T | TCTCTCTC others(9): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0177 | 3 | HG01168.hp1 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-11-9078_-11-9077i others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175941 | |||||
chrX:10175945 | C | CCT | 7 | a0001c0001t0005g0060a0001c0001t0005g0143a0001c0001t0009g0061others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-9052_-11-9051d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175945 | |||||
chrX:10175945 | C | CCTCT | 2 | a0001c0001t0009g0078a0001c0002t0004g0045 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11-9054_-11-9051d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175945 | |||||
chrX:10175945 | C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 165 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-11-9077C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175945 | ||||||
chrX:10175947 | T | TCTCCCCC others(7): Show |
46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(43): Show | 47 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-11-9072_-11-9071i others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175947 | |||||
chrX:10175947 | T | TCTCCCCC others(29): Show |
2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG03834.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-11-9072_-11-9071i others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175947 | |||||
chrX:10175949 | T | TCCCCCCT others(12): Show |
1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-9072_-11-9071i others(21): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175949 | |||||
chrX:10175949 | T | TCCCCCTC others(11): Show |
115 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-11-9072_-11-9071i others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175949 | |||||
chrX:10175951 | T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0177 | 3 | HG01168.hp1 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-11-9071T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175951 | ||||||
chrX:10175953 | T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 49 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.-11-9069T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175953 | ||||||
chrX:10175970 | CTGTGTG | C | 1 | a0001c0002t0004g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11-9044_-11-9039d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10175970 | |||||
chrX:10175972 | G | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11-9050G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175972 | ||||||
chrX:10175974 | G | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(170): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11-9048G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175974 | ||||||
chrX:10175976 | G | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-11-9046G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10175976 | ||||||
chrX:10176617 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-11-8405C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10176617 | ||||||
chrX:10176866 | G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(61): Show | 65 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-11-8156G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10176866 | ||||||
chrX:10177234 | C | T | 7 | a0001c0001t0004g0054a0001c0001t0004g0148a0001c0001t0008g0055others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7788C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177234 | ||||||
chrX:10177271 | C | T | 7 | a0001c0001t0004g0054a0001c0001t0004g0148a0001c0001t0008g0055others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-7751C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177271 | ||||||
chrX:10177455 | T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(77): Show | 81 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.-11-7567T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177455 | ||||||
chrX:10177661 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-11-7361C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177661 | ||||||
chrX:10177742 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-11-7280T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10177742 | ||||||
chrX:10178038 | ATACTGCA others(10): Show |
A | 2 | a0001c0001t0001g0024a0001c0001t0003g0020 | 2 | HG01928.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-11-6964_-11-6948d others(19): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10178038 | |||||
chrX:10178287 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-11-6735G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10178287 | ||||||
chrX:10178342 | T | C | 7 | a0001c0001t0004g0054a0001c0001t0004g0148a0001c0001t0008g0055others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6680T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10178342 | ||||||
chrX:10178512 | G | A | 7 | a0001c0001t0004g0054a0001c0001t0004g0148a0001c0001t0008g0055others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6510G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10178512 | ||||||
chrX:10179063 | T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(77): Show | 81 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.-11-5959T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179063 | ||||||
chrX:10179236 | G | T | 103 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-11-5786G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179236 | ||||||
chrX:10179247 | C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(68): Show | 72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-5775C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179247 | ||||||
chrX:10179259 | A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(68): Show | 72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-5763A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179259 | ||||||
chrX:10179261 | TC | T | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11-5758delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10179261 | |||||
chrX:10179721 | A | G | 1 | a0001c0001t0024g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-11-5301A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179721 | ||||||
chrX:10179754 | C | T | 1 | a0001c0001t0004g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11-5268C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10179754 | ||||||
chrX:10179857 | T | TG | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-5160dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10179857 | |||||
chrX:10180041 | T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(68): Show | 72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-4981T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180041 | ||||||
chrX:10180073 | G | GTT | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-4946_-11-4945d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180073 | |||||
chrX:10180086 | A | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(68): Show | 72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-4936A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180086 | ||||||
chrX:10180091 | G | A | 7 | a0001c0001t0005g0060a0001c0001t0005g0143a0001c0001t0009g0061others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-4931G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180091 | ||||||
chrX:10180201 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4821G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180201 | ||||||
chrX:10180452 | GC | G | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-4567delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180452 | |||||
chrX:10180455 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-11-4567C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180455 | ||||||
chrX:10180640 | G | A | 102 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-11-4382G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180640 | ||||||
chrX:10180707 | C | T | 11 | a0001c0001t0002g0066a0001c0001t0004g0054a0001c0001t0004g0148others(8): Show | 11 | HG01109.hp1 HG02293.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-4315C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180707 | ||||||
chrX:10180767 | C | CA | 85 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0175others(82): Show | 85 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-11-4228dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | C | CAA | 28 | a0001c0001t0001g0172a0001c0001t0001g0225a0001c0001t0001g0230others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11-4229_-11-4228d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | C | CAAA | 4 | a0001c0001t0002g0234a0001c0001t0003g0191a0001c0001t0040g0156others(1): Show | 4 | HG01346.hp2 HG01934.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-4230_-11-4228d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | C | CAAAAAA | 1 | a0001c0001t0002g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11-4233_-11-4228d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | CA | C | 11 | a0001c0001t0001g0091a0001c0001t0004g0054a0001c0001t0004g0148others(8): Show | 11 | HG01109.hp1 HG01168.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-4228delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | CAAA | C | 3 | a0001c0002t0004g0046a0001c0002t0004g0048a0001c0002t0004g0049 | 3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-4230_-11-4228d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | CAAAA | C | 4 | a0001c0001t0002g0021a0001c0001t0002g0146a0001c0001t0003g0012others(1): Show | 4 | HG02723.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-4231_-11-4228d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | CAAAAA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(29): Show | 33 | HG01070.hp1 HG01074.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-4232_-11-4228d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | CAAAAAA | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(13): Show | 16 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11-4233_-11-4228d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180767 | CAAAAAAA | C | 1 | a0001c0001t0002g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-11-4234_-11-4228d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180767 | |||||
chrX:10180785 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0002t0004g0147 | 3 | HG03195.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-11-4233_-11-4224d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180785 | |||||
chrX:10180791 | AAAAG | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-11-4219_-11-4216d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180791 | |||||
chrX:10180841 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11-4181G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180841 | ||||||
chrX:10180846 | G | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11-4176G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180846 | ||||||
chrX:10180877 | A | C | 1 | a0001c0001t0004g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11-4145A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10180877 | ||||||
chrX:10180881 | GC | G | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-4139delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180881 | |||||
chrX:10180889 | AC | A | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-4129delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10180889 | |||||
chrX:10181039 | A | G | 9 | a0001c0001t0001g0188a0001c0001t0001g0202a0001c0001t0001g0204others(6): Show | 9 | HG00639.hp2 HG01099.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-3983A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181039 | ||||||
chrX:10181114 | T | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(67): Show | 71 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-3908T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181114 | ||||||
chrX:10181176 | A | T | 1 | a0001c0001t0011g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-11-3846A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181176 | ||||||
chrX:10181196 | G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0025 | 2 | HG01070.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-11-3826G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181196 | ||||||
chrX:10181201 | TA | T | 2 | a0001c0001t0002g0127a0001c0001t0003g0171 | 2 | NA18956.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-11-3812delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181201 | |||||
chrX:10181236 | G | GT | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-3785dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181236 | |||||
chrX:10181330 | C | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 70 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-3692C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181330 | ||||||
chrX:10181331 | T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 70 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-3691T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181331 | ||||||
chrX:10181339 | A | G | 3 | a0001c0002t0004g0046a0001c0002t0004g0048a0001c0002t0004g0049 | 3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-3683A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181339 | ||||||
chrX:10181354 | G | GA | 1 | a0001c0001t0011g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-11-3658dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181354 | |||||
chrX:10181361 | AAAAG | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 70 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-3653_-11-3650d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181361 | |||||
chrX:10181365 | GAAAGAAA others(8): Show |
G | 5 | a0001c0001t0004g0069a0001c0001t0008g0037a0001c0002t0002g0052others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-3634_-11-3620d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181365 | |||||
chrX:10181444 | TG | T | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-3574delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10181444 | |||||
chrX:10181718 | C | A | 1 | a0001c0002t0004g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-3304C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181718 | ||||||
chrX:10181858 | G | A | 3 | a0001c0002t0004g0046a0001c0002t0004g0048a0001c0002t0004g0049 | 3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-3164G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181858 | ||||||
chrX:10181868 | A | T | 2 | a0001c0001t0005g0060a0001c0001t0005g0143 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-3154A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10181868 | ||||||
chrX:10182448 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-11-2574T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182448 | ||||||
chrX:10182457 | G | A | 4 | a0001c0001t0002g0161a0001c0001t0003g0159a0001c0001t0003g0170others(1): Show | 4 | HG00323.hp1 NA18747.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2565G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182457 | ||||||
chrX:10182465 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-11-2557G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182465 | ||||||
chrX:10182467 | G | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2555G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182467 | ||||||
chrX:10182743 | T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2279T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182743 | ||||||
chrX:10182748 | A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2274A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182748 | ||||||
chrX:10182791 | A | AG | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-2230dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10182791 | |||||
chrX:10182937 | T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-2085T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182937 | ||||||
chrX:10182977 | T | TG | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-2044dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10182977 | |||||
chrX:10182991 | C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(67): Show | 71 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-2031C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10182991 | ||||||
chrX:10183157 | C | T | 2 | a0001c0001t0002g0130a0001c0002t0009g0075 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-1865C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183157 | ||||||
chrX:10183232 | A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 73 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.-11-1790A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183232 | ||||||
chrX:10183271 | G | GT | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-11-1747dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10183271 | |||||
chrX:10183325 | T | G | 1 | a0001c0001t0003g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-11-1697T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183325 | ||||||
chrX:10183387 | G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-11-1635G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183387 | ||||||
chrX:10183592 | C | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(172): Show | 176 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.-11-1430C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183592 | ||||||
chrX:10183772 | A | G | 106 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-11-1250A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183772 | ||||||
chrX:10183832 | A | C | 9 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-1190A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10183832 | ||||||
chrX:10184135 | C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(56): Show | 60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-887C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184135 | ||||||
chrX:10184323 | GC | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(67): Show | 71 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-693delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 10184323 | |||||
chrX:10184428 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-11-594G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184428 | ||||||
chrX:10184585 | T | C | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-437T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184585 | ||||||
chrX:10184599 | G | A | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-423G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184599 | ||||||
chrX:10184847 | T | C | 1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11-175T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 2/12 | chrX | 10184847 | ||||||
chrX:10185334 | A | G | 104 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(101): Show | 104 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.144+158A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185334 | ||||||
chrX:10185413 | C | G | 1 | a0001c0001t0004g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.144+237C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185413 | ||||||
chrX:10185431 | C | G | 1 | a0001c0001t0002g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.144+255C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185431 | ||||||
chrX:10185433 | T | C | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.144+257T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185433 | ||||||
chrX:10185584 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144+408G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185584 | ||||||
chrX:10185623 | G | T | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.144+447G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185623 | ||||||
chrX:10185704 | GC | G | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.144+534delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 10185704 | |||||
chrX:10185710 | C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(2): Show | 5 | HG01081.hp1 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+534C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185710 | ||||||
chrX:10185808 | G | C | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.144+632G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185808 | ||||||
chrX:10185841 | G | A | 7 | a0001c0001t0005g0060a0001c0001t0005g0143a0001c0001t0009g0061others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+665G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185841 | ||||||
chrX:10185849 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.144+673C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10185849 | ||||||
chrX:10186146 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144+970C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186146 | ||||||
chrX:10186176 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.144+1000C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186176 | ||||||
chrX:10186229 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.144+1053G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186229 | ||||||
chrX:10186255 | G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(56): Show | 60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.144+1079G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186255 | ||||||
chrX:10186560 | G | A | 102 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.145-955G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186560 | ||||||
chrX:10186608 | G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.145-907G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186608 | ||||||
chrX:10186629 | G | T | 105 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.145-886G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186629 | ||||||
chrX:10186874 | C | T | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-641C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186874 | ||||||
chrX:10186940 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.145-575C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10186940 | ||||||
chrX:10187343 | G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(56): Show | 60 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.145-172G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10187343 | ||||||
chrX:10187473 | G | A | 2 | a0001c0001t0009g0078a0001c0002t0004g0045 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.145-42G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 3/12 | chrX | 10187473 | ||||||
chrX:10187618 | C | G | 5 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.244+4C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10187618 | ||||||
chrX:10187681 | C | T | 4 | a0001c0001t0002g0152a0001c0001t0004g0151a0001c0001t0005g0149others(1): Show | 4 | HG02559.hp2 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+67C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10187681 | ||||||
chrX:10187719 | CT | C | 1 | a0001c0001t0001g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.244+109delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10187719 | |||||
chrX:10187721 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.244+107T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10187721 | ||||||
chrX:10188107 | T | TG | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.244+497dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10188107 | |||||
chrX:10188143 | T | C | 3 | a0001c0002t0004g0050a0001c0002t0004g0106a0001c0002t0026g0034 | 3 | HG01074.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.244+529T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188143 | ||||||
chrX:10188198 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.244+584A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188198 | ||||||
chrX:10188244 | G | T | 6 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+630G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188244 | ||||||
chrX:10188335 | TG | T | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.244+724delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10188335 | |||||
chrX:10188509 | A | G | 1 | a0001c0001t0008g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.244+895A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188509 | ||||||
chrX:10188969 | G | A | 103 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.244+1355G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10188969 | ||||||
chrX:10189096 | A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(87): Show | 91 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.244+1482A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189096 | ||||||
chrX:10189377 | G | T | 23 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.244+1763G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189377 | ||||||
chrX:10189489 | G | A | 1 | a0001c0002t0004g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244+1875G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189489 | ||||||
chrX:10189750 | AG | A | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.244+2138delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10189750 | |||||
chrX:10189770 | T | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(90): Show | 94 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(91): Show |
intron_variant | MODIFIER | c.244+2156T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189770 | ||||||
chrX:10189837 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.244+2223G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10189837 | ||||||
chrX:10190072 | G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.244+2458G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190072 | ||||||
chrX:10190113 | C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(199): Show | 203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.244+2499C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190113 | ||||||
chrX:10190306 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+2692C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190306 | ||||||
chrX:10190720 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.244+3106C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10190720 | ||||||
chrX:10191387 | A | C | 1 | a0001c0001t0003g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.245-3524A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191387 | ||||||
chrX:10191542 | G | A | 4 | a0001c0001t0002g0130a0001c0001t0006g0062a0001c0001t0034g0073others(1): Show | 4 | HG03195.hp1 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-3369G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191542 | ||||||
chrX:10191618 | T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 93 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.245-3293T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191618 | ||||||
chrX:10191692 | A | AATTTTTT | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245-3219_245-3218i others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191692 | ||||||
chrX:10191692 | A | AT | 94 | a0001c0001t0001g0089a0001c0001t0001g0115a0001c0001t0001g0117others(91): Show | 94 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.245-3191dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATT | 29 | a0001c0001t0001g0072a0001c0001t0001g0183a0001c0001t0001g0184others(26): Show | 29 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.245-3192_245-3191d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTT | 8 | a0001c0001t0001g0236a0001c0001t0001g0252a0001c0001t0002g0119others(5): Show | 8 | HG00438.hp2 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-3193_245-3191d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTT | 1 | a0001c0001t0006g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.245-3194_245-3191d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTT | 2 | a0001c0001t0002g0146a0001c0002t0004g0085 | 2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.245-3195_245-3191d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTT | 1 | a0001c0001t0034g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.245-3196_245-3191d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT | 2 | a0001c0001t0009g0078a0001c0002t0004g0045 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.245-3197_245-3191d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(2): Show |
2 | a0001c0001t0005g0060a0001c0001t0005g0143 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.245-3199_245-3191d others(11): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(9): Show |
1 | a0001c0002t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.245-3206_245-3191d others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0002g0094a0001c0001t0006g0064a0001c0001t0032g0067 | 3 | HG02622.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.245-3207_245-3191d others(19): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(11): Show |
5 | a0001c0001t0002g0096a0001c0001t0006g0063a0001c0001t0006g0065others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-3208_245-3191d others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(13): Show |
1 | a0001c0008t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.245-3210_245-3191d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0002g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.245-3211_245-3191d others(23): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0002g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-3212_245-3191d others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | A | ATTTTTTT others(19): Show |
1 | a0001c0001t0029g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.245-3216_245-3191d others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | AT | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0002g0010others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.245-3191delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | ATT | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(33): Show | 37 | HG00609.hp1 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.245-3192_245-3191d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | ATTT | A | 14 | a0001c0001t0001g0013a0001c0001t0002g0044a0001c0001t0004g0093others(11): Show | 14 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.245-3193_245-3191d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | ATTTT | A | 1 | a0001c0001t0004g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-3194_245-3191d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | ATTTTT | A | 3 | a0001c0001t0040g0156a0001c0002t0004g0046a0001c0002t0039g0155 | 3 | HG01346.hp2 HG02602.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.245-3195_245-3191d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | ATTTTTT | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-3196_245-3191d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191692 | ATTTTTTT others(1): Show |
A | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.245-3198_245-3191d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10191692 | |||||
chrX:10191966 | C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(31): Show | 35 | HG00609.hp1 HG01070.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.245-2945C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10191966 | ||||||
chrX:10192175 | A | AC | 9 | a0001c0001t0002g0130a0001c0001t0004g0054a0001c0001t0004g0148others(6): Show | 9 | HG01109.hp1 HG02293.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.245-2730dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192175 | |||||
chrX:10192244 | T | TAC | 13 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0144others(10): Show | 13 | HG02083.hp1 HG02132.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.245-2640_245-2639d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | |||||
chrX:10192244 | T | TACAC | 19 | a0001c0001t0001g0115a0001c0001t0002g0130a0001c0001t0002g0146others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.245-2642_245-2639d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | |||||
chrX:10192244 | T | TACACAC | 2 | a0001c0001t0040g0156a0001c0002t0004g0085 | 2 | HG01346.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.245-2644_245-2639d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | |||||
chrX:10192244 | T | TACACACA others(3): Show |
10 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-2648_245-2639d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | |||||
chrX:10192244 | T | TACACACA others(5): Show |
3 | a0001c0002t0004g0046a0001c0002t0004g0048a0001c0002t0004g0049 | 3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.245-2650_245-2639d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | |||||
chrX:10192244 | T | TACACACA others(7): Show |
1 | a0001c0001t0002g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245-2652_245-2639d others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192244 | |||||
chrX:10192286 | AAGAG | A | 11 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-2622_245-2619d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192286 | |||||
chrX:10192342 | C | A | 1 | a0001c0001t0034g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.245-2569C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192342 | ||||||
chrX:10192438 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.245-2473A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192438 | ||||||
chrX:10192535 | T | TG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-2372dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192535 | |||||
chrX:10192598 | G | C | 23 | a0001c0001t0002g0130a0001c0001t0002g0146a0001c0001t0004g0054others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.245-2313G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192598 | ||||||
chrX:10192803 | T | C | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.245-2108T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192803 | ||||||
chrX:10192874 | T | G | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.245-2037T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10192874 | ||||||
chrX:10192960 | TC | T | 1 | a0001c0001t0007g0142 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.245-1948delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10192960 | |||||
chrX:10193030 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.245-1881G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193030 | ||||||
chrX:10193060 | A | G | 1 | a0001c0001t0003g0222 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.245-1851A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193060 | ||||||
chrX:10193195 | GA | G | 1 | a0001c0001t0004g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.245-1714delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193195 | |||||
chrX:10193254 | G | A | 5 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-1657G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193254 | ||||||
chrX:10193259 | G | A | 2 | a0001c0002t0004g0050a0001c0002t0004g0106 | 2 | HG01074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.245-1652G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193259 | ||||||
chrX:10193561 | G | A | 206 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.245-1350G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193561 | ||||||
chrX:10193568 | TG | T | 1 | a0001c0001t0003g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.245-1341delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193568 | |||||
chrX:10193613 | G | A | 1 | a0001c0001t0004g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.245-1298G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193613 | ||||||
chrX:10193859 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.245-1052C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193859 | ||||||
chrX:10193861 | T | G | 110 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(107): Show | 110 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.245-1050T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10193861 | ||||||
chrX:10193961 | G | GT | 108 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0172others(105): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.245-938dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | |||||
chrX:10193961 | G | GTT | 1 | a0001c0001t0001g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.245-939_245-938dup others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | |||||
chrX:10193961 | GT | G | 70 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.245-938delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | |||||
chrX:10193961 | GTT | G | 5 | a0001c0001t0002g0146a0001c0001t0005g0079a0001c0002t0004g0046others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-939_245-938del others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10193961 | |||||
chrX:10194120 | A | AG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-787dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194120 | |||||
chrX:10194154 | T | C | 18 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.245-757T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194154 | ||||||
chrX:10194173 | G | GA | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-736dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194173 | |||||
chrX:10194184 | G | A | 60 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.245-727G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194184 | ||||||
chrX:10194222 | G | T | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-689G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194222 | ||||||
chrX:10194398 | A | AG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-512dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194398 | |||||
chrX:10194410 | TA | T | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-498delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194410 | |||||
chrX:10194439 | A | AT | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-469dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194439 | |||||
chrX:10194558 | GC | G | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-349delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194558 | |||||
chrX:10194622 | A | G | 2 | a0001c0002t0037g0032a0001c0002t0038g0033 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.245-289A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194622 | ||||||
chrX:10194795 | C | CCT | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-116_245-115ins others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194795 | ||||||
chrX:10194835 | T | TC | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-75dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194835 | |||||
chrX:10194840 | C | T | 2 | a0001c0001t0011g0247a0001c0001t0035g0231 | 2 | NA18997.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.245-71C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194840 | ||||||
chrX:10194860 | T | TC | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-51_245-50insC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | chrX | 10194860 | ||||||
chrX:10194899 | T | TA | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.245-11dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chrX | 10194899 | |||||
chrX:10195103 | G | GT | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | splice_region_variant&intron_variant | LOW | c.432+6dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195103 | |||||
chrX:10195108 | T | TG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+13dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195108 | |||||
chrX:10195127 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.432+29G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195127 | ||||||
chrX:10195138 | G | A | 5 | a0001c0001t0002g0146a0001c0001t0005g0079a0001c0002t0004g0046others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.432+40G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195138 | ||||||
chrX:10195158 | T | TG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+61dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195158 | |||||
chrX:10195206 | G | GC | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+109dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195206 | |||||
chrX:10195217 | C | T | 16 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.432+119C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195217 | ||||||
chrX:10195241 | CT | C | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+148delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195241 | |||||
chrX:10195314 | C | CAT | 2 | a0001c0001t0001g0200a0001c0001t0024g0209 | 2 | NA19066.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.432+232_432+233dup others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195314 | |||||
chrX:10195314 | CAT | C | 11 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+232_432+233del others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195314 | |||||
chrX:10195390 | GA | G | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+294delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195390 | |||||
chrX:10195426 | T | TG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+329dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195426 | |||||
chrX:10195457 | TA | T | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+361delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195457 | |||||
chrX:10195477 | TA | T | 1 | a0001c0001t0001g0199 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.432+387delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195477 | |||||
chrX:10195523 | A | AC | 2 | a0001c0001t0001g0208a0001c0001t0006g0064 | 2 | HG01496.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.432+428dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195523 | |||||
chrX:10195523 | A | ACTG | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+426_432+427ins others(3): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195523 | |||||
chrX:10195524 | C | CA | 1 | a0001c0001t0004g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+426_432+427ins others(1): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195524 | ||||||
chrX:10195574 | C | T | 6 | a0001c0001t0001g0199a0001c0001t0002g0146a0001c0001t0005g0079others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+476C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195574 | ||||||
chrX:10195840 | G | A | 25 | a0001c0001t0002g0130a0001c0001t0002g0146a0001c0001t0004g0054others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.432+742G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195840 | ||||||
chrX:10195865 | A | AACC | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+767_432+768ins others(3): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195865 | ||||||
chrX:10195866 | C | A | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+768C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10195866 | ||||||
chrX:10195995 | A | AT | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+898dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10195995 | |||||
chrX:10196059 | C | T | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+961C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196059 | ||||||
chrX:10196066 | A | G | 229 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.432+968A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196066 | ||||||
chrX:10196138 | T | C | 11 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+1040T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196138 | ||||||
chrX:10196163 | A | AT | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+1066dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196163 | |||||
chrX:10196202 | G | GTC | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+1105_432+1106d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196202 | |||||
chrX:10196275 | C | CA | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+1178dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196275 | |||||
chrX:10196282 | G | T | 24 | a0001c0001t0002g0130a0001c0001t0002g0146a0001c0001t0004g0054others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.432+1184G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196282 | ||||||
chrX:10196325 | G | GA | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+1228dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196325 | |||||
chrX:10196495 | T | G | 206 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.432+1397T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196495 | ||||||
chrX:10196538 | C | CTTT | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.433-1386_433-1384d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | C | CTTTT | 12 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-1387_433-1384d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | C | CTTTTT | 15 | a0001c0001t0002g0130a0001c0001t0004g0054a0001c0001t0005g0060others(12): Show | 15 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-1388_433-1384d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | C | CTTTTTT | 11 | a0001c0001t0004g0092a0001c0001t0004g0148a0001c0001t0005g0079others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1389_433-1384d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | C | CTTTTTTT | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(47): Show | 51 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.433-1390_433-1384d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | C | CTTTTTTT others(1): Show |
3 | a0001c0001t0001g0015a0001c0001t0003g0020a0001c0002t0013g0035 | 3 | HG03486.hp1 NA18943.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.433-1391_433-1384d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | C | CTTTTTTT others(2): Show |
1 | a0001c0001t0003g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.433-1392_433-1384d others(11): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196538 | CT | C | 61 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.433-1384delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10196538 | |||||
chrX:10196651 | A | G | 1 | a0001c0001t0004g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.433-1288A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196651 | ||||||
chrX:10196687 | T | C | 38 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(35): Show | 38 | HG01109.hp1 HG01243.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.433-1252T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196687 | ||||||
chrX:10196768 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-1171G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196768 | ||||||
chrX:10196969 | G | T | 58 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.433-970G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10196969 | ||||||
chrX:10197363 | T | A | 170 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.433-576T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197363 | ||||||
chrX:10197507 | G | A | 3 | a0001c0002t0004g0046a0001c0002t0004g0048a0001c0002t0004g0049 | 3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.433-432G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197507 | ||||||
chrX:10197519 | G | T | 4 | a0001c0001t0002g0146a0001c0002t0004g0046a0001c0002t0004g0048others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-420G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197519 | ||||||
chrX:10197560 | A | G | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-379A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197560 | ||||||
chrX:10197742 | CTGTT | C | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.433-193_433-190del others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chrX | 10197742 | |||||
chrX:10197755 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.433-184C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 5/12 | chrX | 10197755 | ||||||
chrX:10198076 | A | AT | 3 | a0001c0001t0003g0171a0001c0001t0005g0060a0001c0001t0005g0143 | 3 | HG02809.hp2 HG03139.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.555+22dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10198076 | |||||
chrX:10198117 | A | AAT | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.555+56_555+57insAT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198117 | ||||||
chrX:10198119 | C | CCAAA | 1 | a0001c0001t0002g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.555+58_555+59insCA others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198119 | ||||||
chrX:10198158 | A | C | 73 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.555+97A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198158 | ||||||
chrX:10198437 | C | T | 5 | a0001c0001t0009g0078a0001c0002t0004g0045a0001c0002t0004g0046others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+376C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198437 | ||||||
chrX:10198615 | G | A | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.555+554G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198615 | ||||||
chrX:10198623 | G | A | 1 | a0001c0001t0001g0089 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.555+562G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198623 | ||||||
chrX:10198774 | C | G | 1 | a0001c0001t0001g0089 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.555+713C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198774 | ||||||
chrX:10198842 | C | G | 11 | a0001c0001t0002g0066a0001c0001t0002g0146a0001c0001t0006g0063others(8): Show | 11 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+781C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198842 | ||||||
chrX:10198884 | C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(68): Show | 72 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.555+823C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198884 | ||||||
chrX:10198984 | C | T | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.555+923C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10198984 | ||||||
chrX:10199082 | A | G | 1 | a0001c0001t0006g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555+1021A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10199082 | ||||||
chrX:10199515 | ACAG | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(128): Show | 132 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.555+1458_555+1460d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10199515 | |||||
chrX:10199849 | C | T | 1 | a0001c0002t0004g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.555+1788C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10199849 | ||||||
chrX:10199906 | G | GT | 9 | a0001c0001t0005g0060a0001c0001t0005g0143a0001c0001t0009g0061others(6): Show | 9 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+1846dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10199906 | |||||
chrX:10200031 | G | A | 1 | a0001c0007t0012g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.555+1970G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200031 | ||||||
chrX:10200066 | T | A | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.555+2005T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200066 | ||||||
chrX:10200257 | A | C | 7 | a0001c0001t0002g0066a0001c0001t0002g0146a0001c0001t0006g0063others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+2196A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200257 | ||||||
chrX:10200582 | C | G | 61 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.555+2521C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200582 | ||||||
chrX:10200661 | G | T | 61 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.555+2600G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200661 | ||||||
chrX:10200729 | C | T | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.555+2668C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10200729 | ||||||
chrX:10201051 | AT | A | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0135others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+2991delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201051 | ||||||
chrX:10201091 | G | A | 61 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.555+3030G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201091 | ||||||
chrX:10201202 | G | C | 10 | a0001c0001t0002g0130a0001c0001t0005g0060a0001c0001t0005g0143others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+3141G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201202 | ||||||
chrX:10201272 | G | A | 1 | a0001c0002t0004g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.555+3211G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201272 | ||||||
chrX:10201417 | A | G | 2 | a0001c0001t0004g0069a0001c0002t0004g0134 | 2 | HG02615.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.555+3356A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201417 | ||||||
chrX:10201648 | G | A | 11 | a0001c0001t0004g0051a0001c0001t0004g0148a0001c0001t0008g0055others(8): Show | 11 | HG01109.hp1 HG01346.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+3587G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201648 | ||||||
chrX:10201664 | C | T | 10 | a0001c0001t0002g0130a0001c0001t0005g0060a0001c0001t0005g0143others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+3603C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201664 | ||||||
chrX:10201706 | C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(210): Show | 214 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.555+3645C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201706 | ||||||
chrX:10201835 | C | T | 3 | a0001c0001t0002g0161a0001c0001t0003g0159a0001c0001t0003g0170 | 3 | HG00323.hp1 NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.555+3774C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201835 | ||||||
chrX:10201835 | CG | C | 2 | a0001c0001t0002g0193a0001c0001t0003g0195 | 2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.555+3779delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10201835 | |||||
chrX:10201941 | C | G | 2 | a0001c0001t0007g0141a0001c0001t0007g0142 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.555+3880C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201941 | ||||||
chrX:10201999 | A | C | 51 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.555+3938A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10201999 | ||||||
chrX:10202115 | T | C | 3 | a0001c0001t0002g0130a0001c0001t0006g0062a0001c0002t0009g0075 | 3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.555+4054T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202115 | ||||||
chrX:10202231 | T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 127 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.556-4127T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202231 | ||||||
chrX:10202245 | G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0014g0003others(1): Show | 4 | HG02273.hp1 NA18942.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-4113G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202245 | ||||||
chrX:10202324 | A | G | 51 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.556-4034A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202324 | ||||||
chrX:10202414 | A | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.556-3944A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202414 | ||||||
chrX:10202638 | C | CA | 6 | a0001c0001t0001g0257a0001c0001t0002g0119a0001c0001t0003g0140others(3): Show | 6 | HG01192.hp1 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-3688dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | C | CAA | 4 | a0001c0001t0004g0092a0001c0001t0004g0093a0001c0001t0022g0118others(1): Show | 4 | HG01346.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-3689_556-3688d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | C | CAAA | 1 | a0001c0002t0039g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.556-3690_556-3688d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CA | C | 36 | a0001c0001t0001g0126a0001c0001t0001g0154a0001c0001t0001g0183others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.556-3688delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAA | C | 13 | a0001c0001t0003g0157a0001c0001t0003g0185a0001c0001t0003g0189others(10): Show | 13 | HG01109.hp1 HG02293.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-3689_556-3688d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAA | C | 7 | a0001c0001t0002g0066a0001c0001t0006g0063a0001c0001t0006g0064others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.556-3690_556-3688d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAA | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0184others(15): Show | 18 | HG01081.hp1 HG01123.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.556-3691_556-3688d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAA | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(93): Show | 97 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.556-3692_556-3688d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAAA | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0199a0001c0001t0001g0215others(7): Show | 10 | HG01884.hp2 HG02735.hp1 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.556-3693_556-3688d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAAAA | C | 6 | a0001c0001t0001g0144a0001c0001t0002g0094a0001c0001t0002g0096others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-3694_556-3688d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0002g0130a0001c0001t0005g0060a0001c0001t0005g0143others(6): Show | 9 | HG02630.hp1 HG02809.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.556-3695_556-3688d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAAAA others(2): Show |
C | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.556-3696_556-3688d others(11): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0012g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.556-3700_556-3688d others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202638 | CAAAAAAA others(8): Show |
C | 8 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.556-3702_556-3688d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10202638 | |||||
chrX:10202697 | G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(129): Show | 133 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.556-3661G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202697 | ||||||
chrX:10202697 | G | T | 10 | a0001c0001t0002g0130a0001c0001t0005g0060a0001c0001t0005g0143others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.556-3661G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202697 | ||||||
chrX:10202922 | C | T | 7 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-3436C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202922 | ||||||
chrX:10202952 | C | T | 3 | a0001c0001t0003g0174a0001c0001t0003g0192a0002c0004t0003g0196 | 3 | NA18612.hp1 NA18974.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.556-3406C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10202952 | ||||||
chrX:10203025 | A | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.556-3333A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10203025 | ||||||
chrX:10203386 | G | C | 1 | a0001c0001t0004g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.556-2972G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10203386 | ||||||
chrX:10204025 | C | T | 3 | a0001c0001t0002g0130a0001c0001t0006g0062a0001c0002t0009g0075 | 3 | HG03195.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.556-2333C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10204025 | ||||||
chrX:10204135 | A | G | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.556-2223A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10204135 | ||||||
chrX:10204480 | TA | T | 2 | a0001c0001t0002g0130a0001c0002t0009g0075 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.556-1873delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204480 | |||||
chrX:10204613 | C | CT | 32 | a0001c0001t0001g0072a0001c0001t0001g0110a0001c0001t0001g0123others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.556-1709dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTT | 52 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0027others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.556-1710_556-1709d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTT | 30 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0023others(27): Show | 31 | HG01255.hp1 HG01257.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.556-1711_556-1709d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTT | 47 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0172others(44): Show | 47 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.556-1712_556-1709d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTT | 16 | a0001c0001t0001g0024a0001c0001t0001g0162a0001c0001t0001g0186others(13): Show | 16 | HG00438.hp1 HG01258.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.556-1713_556-1709d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTT | 8 | a0001c0001t0001g0217a0001c0001t0001g0232a0001c0001t0001g0235others(5): Show | 8 | HG02027.hp1 HG02074.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.556-1714_556-1709d others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTTT | 2 | a0001c0001t0003g0191a0001c0001t0003g0224 | 2 | HG01934.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.556-1715_556-1709d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTTT others(1): Show |
3 | a0001c0001t0003g0185a0001c0001t0004g0092a0001c0001t0004g0093 | 3 | HG01516.hp2 HG01517.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.556-1716_556-1709d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTTT others(2): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0238 | 2 | HG01943.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.556-1717_556-1709d others(11): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0032g0067a0001c0001t0040g0156a0001c0002t0039g0155 | 3 | HG01346.hp2 HG02602.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.556-1720_556-1709d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0006g0065a0001c0001t0034g0073 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.556-1721_556-1709d others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | C | CTTTTTTT others(7): Show |
5 | a0001c0001t0002g0066a0001c0001t0002g0146a0001c0001t0006g0063others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-1722_556-1709d others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CT | C | 2 | a0001c0001t0001g0089a0001c0001t0002g0127 | 2 | NA18981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.556-1709delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTT | C | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.556-1710_556-1709d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT | C | 3 | a0001c0001t0005g0079a0001c0002t0004g0046a0001c0002t0004g0048 | 3 | HG02647.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.556-1715_556-1709d others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(1): Show |
C | 3 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0002t0004g0049 | 3 | HG02976.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.556-1716_556-1709d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(2): Show |
C | 2 | a0001c0001t0001g0016a0001c0002t0004g0031 | 2 | HG02622.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.556-1717_556-1709d others(11): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.556-1718_556-1709d others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0244a0001c0001t0003g0157a0001c0001t0005g0060others(3): Show | 6 | HG02040.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-1719_556-1709d others(13): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0249a0001c0001t0002g0130a0001c0001t0006g0062others(3): Show | 6 | HG02965.hp1 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1720_556-1709d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.556-1721_556-1709d others(15): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0004g0069 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.556-1723_556-1709d others(17): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(9): Show |
C | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(2): Show | 5 | HG01123.hp2 HG02273.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-1724_556-1709d others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204613 | CTTTTTTT others(13): Show |
C | 16 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.556-1728_556-1709d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204613 | |||||
chrX:10204615 | T | TTTA | 1 | a0001c0001t0003g0178 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.556-1741_556-1740i others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10204615 | |||||
chrX:10204992 | C | T | 1 | a0001c0007t0012g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.556-1366C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10204992 | ||||||
chrX:10205240 | A | G | 6 | a0001c0001t0001g0126a0001c0001t0002g0105a0001c0001t0002g0124others(3): Show | 6 | NA18944.hp1 NA18968.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1118A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205240 | ||||||
chrX:10205256 | A | G | 6 | a0001c0001t0001g0126a0001c0001t0002g0105a0001c0001t0002g0124others(3): Show | 6 | NA18944.hp1 NA18968.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1102A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205256 | ||||||
chrX:10205259 | A | G | 6 | a0001c0001t0001g0126a0001c0001t0002g0105a0001c0001t0002g0124others(3): Show | 6 | NA18944.hp1 NA18968.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-1099A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205259 | ||||||
chrX:10205269 | G | C | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-1089G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205269 | ||||||
chrX:10205273 | T | A | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-1085T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205273 | ||||||
chrX:10205428 | G | T | 19 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(16): Show | 19 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.556-930G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205428 | ||||||
chrX:10205447 | T | A | 1 | a0001c0001t0002g0019 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.556-911T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205447 | ||||||
chrX:10205472 | C | CA | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(122): Show | 126 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.556-868dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205472 | |||||
chrX:10205472 | C | CAA | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0235others(10): Show | 13 | HG02074.hp1 HG02622.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.556-869_556-868dup others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205472 | |||||
chrX:10205472 | C | CAAA | 1 | a0001c0001t0001g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.556-870_556-868dup others(3): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205472 | |||||
chrX:10205472 | CA | C | 3 | a0001c0001t0002g0139a0001c0001t0005g0060a0001c0001t0005g0143 | 3 | HG02809.hp2 HG03139.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.556-868delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205472 | |||||
chrX:10205484 | AAAAAAAG | A | 5 | a0001c0001t0004g0148a0001c0001t0006g0062a0001c0001t0008g0055others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-868_556-862del others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205484 | |||||
chrX:10205485 | AAAAAAG | A | 7 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0017g0057others(4): Show | 7 | HG02717.hp1 HG02886.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-863_556-858del others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205485 | |||||
chrX:10205516 | ATGTTCT | A | 1 | a0001c0001t0004g0263 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.556-832_556-827del others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205516 | |||||
chrX:10205607 | C | CT | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0217others(4): Show | 7 | HG01346.hp2 HG02135.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-733dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205607 | |||||
chrX:10205607 | C | CTT | 1 | a0001c0002t0039g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.556-734_556-733dup others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205607 | |||||
chrX:10205607 | CT | C | 30 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.556-733delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205607 | |||||
chrX:10205607 | CTT | C | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.556-734_556-733del others(2): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205607 | |||||
chrX:10205660 | T | TGTAGTG | 1 | a0001c0001t0002g0166 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.556-696_556-691dup others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205660 | |||||
chrX:10205751 | G | T | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.556-607G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205751 | ||||||
chrX:10205758 | T | C | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-600T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10205758 | ||||||
chrX:10205784 | CT | C | 6 | a0001c0001t0005g0079a0001c0001t0005g0149a0001c0001t0005g0150others(3): Show | 6 | HG02647.hp1 HG02976.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-563delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 10205784 | |||||
chrX:10206049 | T | C | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.556-309T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10206049 | ||||||
chrX:10206099 | G | A | 7 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-259G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10206099 | ||||||
chrX:10206346 | C | T | 52 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.556-12C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 6/12 | chrX | 10206346 | ||||||
chrX:10206895 | G | GT | 2 | a0001c0001t0004g0069a0001c0001t0022g0118 | 2 | HG02897.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.843+129dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206895 | |||||
chrX:10206900 | T | TTTTTGTT others(3): Show |
19 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(16): Show | 19 | HG01109.hp1 HG02293.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.843+128_843+129ins others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206900 | |||||
chrX:10206901 | T | TTTTG | 2 | a0001c0001t0009g0061a0001c0001t0013g0077 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.843+128_843+129ins others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206901 | |||||
chrX:10206905 | T | TTGTTTTG | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0003g0160others(3): Show | 6 | HG01257.hp2 HG01258.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.843+129_843+130ins others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10206905 | ||||||
chrX:10206905 | T | TTGTTTTG others(6): Show |
41 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(38): Show | 41 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.843+129_843+130ins others(13): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10206905 | ||||||
chrX:10206906 | G | GT | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.843+134dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206906 | |||||
chrX:10206906 | G | GTTTTGT | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(120): Show | 124 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.843+153_843+158dup others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206906 | |||||
chrX:10206906 | G | GTTTTGTT others(5): Show |
17 | a0001c0001t0002g0066a0001c0001t0002g0094a0001c0001t0002g0096others(14): Show | 17 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.843+147_843+158dup others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 10206906 | |||||
chrX:10206906 | G | T | 47 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.843+130G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10206906 | ||||||
chrX:10207128 | T | G | 1 | a0001c0001t0009g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.843+352T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207128 | ||||||
chrX:10207196 | C | T | 1 | a0001c0002t0004g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.843+420C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207196 | ||||||
chrX:10207225 | G | C | 12 | a0001c0001t0002g0130a0001c0001t0005g0060a0001c0001t0005g0143others(9): Show | 12 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+449G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207225 | ||||||
chrX:10207348 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.843+572C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207348 | ||||||
chrX:10207421 | G | A | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-624G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207421 | ||||||
chrX:10207440 | C | T | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-605C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207440 | ||||||
chrX:10207512 | T | C | 21 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-533T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207512 | ||||||
chrX:10207551 | GTTTT | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0014g0003others(1): Show | 4 | HG02273.hp1 NA18942.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-493_844-490del others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207551 | ||||||
chrX:10207682 | C | A | 3 | a0001c0001t0005g0079a0001c0001t0005g0149a0001c0001t0005g0150 | 3 | NA19030.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.844-363C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207682 | ||||||
chrX:10207702 | A | G | 22 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(19): Show | 22 | HG01109.hp1 HG02055.hp1 HG02293.hp2 others(19): Show |
intron_variant | MODIFIER | c.844-343A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207702 | ||||||
chrX:10207882 | C | T | 7 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-163C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 8/12 | chrX | 10207882 | ||||||
chrX:10208670 | G | A | 7 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+80G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208670 | ||||||
chrX:10208741 | A | G | 52 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0183others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1389+151A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208741 | ||||||
chrX:10208897 | TC | T | 1 | a0001c0001t0003g0170 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1389+310delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10208897 | |||||
chrX:10208934 | G | A | 2 | a0001c0001t0002g0226a0001c0001t0003g0198 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1389+344G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208934 | ||||||
chrX:10208991 | T | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 211 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1389+401T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10208991 | ||||||
chrX:10209089 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1389+499C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209089 | ||||||
chrX:10209200 | AG | A | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1389+614delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209200 | |||||
chrX:10209255 | G | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1389+665G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209255 | ||||||
chrX:10209267 | T | TCCTC | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 121 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.1389+701_1389+704d others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | |||||
chrX:10209267 | T | TCCTCCCT others(1): Show |
60 | a0001c0001t0001g0016a0001c0001t0001g0154a0001c0001t0001g0197others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1389+697_1389+704d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | |||||
chrX:10209267 | T | TCCTCCCT others(5): Show |
2 | a0001c0001t0001g0183a0001c0001t0001g0246 | 2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1389+693_1389+704d others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | |||||
chrX:10209267 | T | TCCTCCCT others(13): Show |
1 | a0001c0001t0001g0252 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1389+685_1389+704d others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | |||||
chrX:10209267 | TCCTCCCT others(1): Show |
T | 7 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+697_1389+704d others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209267 | |||||
chrX:10209289 | C | CTCCCTCC others(18): Show |
4 | a0001c0002t0002g0074a0001c0003t0016g0086a0001c0003t0016g0087others(1): Show | 4 | HG02630.hp1 HG03516.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+704_1389+705i others(27): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209289 | |||||
chrX:10209289 | C | CTCCCTCC others(14): Show |
3 | a0001c0001t0009g0061a0001c0002t0004g0085a0001c0002t0013g0035 | 3 | HG02965.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1389+704_1389+705i others(23): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209289 | |||||
chrX:10209289 | C | CTCCCTCC others(10): Show |
2 | a0001c0001t0005g0060a0001c0001t0005g0143 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1389+704_1389+705i others(19): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209289 | |||||
chrX:10209356 | T | TC | 1 | a0001c0001t0003g0237 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1389+767dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209356 | |||||
chrX:10209371 | CT | C | 1 | a0001c0001t0002g0119 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1389+784delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209371 | |||||
chrX:10209376 | C | CCCCTT | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 213 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1389+794_1389+798d others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209376 | |||||
chrX:10209393 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1389+803G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209393 | ||||||
chrX:10209433 | T | A | 1 | a0001c0001t0003g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1389+843T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209433 | ||||||
chrX:10209545 | A | G | 4 | a0001c0001t0005g0079a0001c0002t0004g0046a0001c0002t0004g0048others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+955A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209545 | ||||||
chrX:10209778 | G | A | 1 | a0001c0001t0003g0020 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1389+1188G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209778 | ||||||
chrX:10209829 | C | CT | 10 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389+1254dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209829 | |||||
chrX:10209829 | CT | C | 9 | a0001c0001t0001g0072a0001c0001t0002g0260a0001c0001t0003g0189others(6): Show | 9 | HG01081.hp2 HG01168.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1389+1254delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10209829 | |||||
chrX:10209973 | C | T | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0135others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+1383C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10209973 | ||||||
chrX:10210029 | CA | C | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1389+1441delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210029 | |||||
chrX:10210238 | T | C | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1389+1648T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210238 | ||||||
chrX:10210355 | T | TC | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1389+1765_1389+176 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210355 | ||||||
chrX:10210359 | G | GT | 1 | a0001c0001t0003g0237 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1389+1772dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210359 | |||||
chrX:10210382 | C | CA | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1389+1792_1389+179 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210382 | ||||||
chrX:10210446 | G | GT | 1 | a0001c0001t0003g0237 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1389+1858dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210446 | |||||
chrX:10210474 | A | AG | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1389+1884_1389+188 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210474 | ||||||
chrX:10210485 | T | A | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1389+1895T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210485 | ||||||
chrX:10210495 | A | AT | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1389+1909dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210495 | |||||
chrX:10210504 | A | AT | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1389+1919dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210504 | |||||
chrX:10210547 | TC | T | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-1917delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210547 | |||||
chrX:10210555 | TG | T | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-1910delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210555 | |||||
chrX:10210569 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1390-1898T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210569 | ||||||
chrX:10210585 | TC | T | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1880delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210585 | |||||
chrX:10210601 | CA | C | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1863delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210601 | |||||
chrX:10210650 | C | CT | 58 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0154others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1390-1795dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210650 | |||||
chrX:10210650 | C | CTT | 8 | a0001c0001t0001g0206a0001c0001t0003g0140a0001c0001t0003g0211others(5): Show | 8 | HG00323.hp2 HG01257.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1796_1390-179 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210650 | |||||
chrX:10210650 | CT | C | 7 | a0001c0001t0004g0070a0001c0001t0004g0151a0001c0001t0009g0061others(4): Show | 7 | HG01256.hp1 HG02602.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-1795delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210650 | |||||
chrX:10210692 | GT | G | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1773delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210692 | |||||
chrX:10210809 | A | AG | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1657dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210809 | |||||
chrX:10210814 | AT | A | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-1648delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210814 | |||||
chrX:10210822 | A | AT | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1639dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210822 | |||||
chrX:10210872 | TC | T | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-1593delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210872 | |||||
chrX:10210927 | C | T | 9 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0097others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1390-1540C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210927 | ||||||
chrX:10210932 | G | C | 8 | a0001c0001t0002g0066a0001c0001t0002g0146a0001c0001t0006g0063others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1535G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210932 | ||||||
chrX:10210939 | C | CT | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1528_1390-152 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210939 | ||||||
chrX:10210941 | C | CTCG | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1526_1390-152 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210941 | ||||||
chrX:10210954 | G | GC | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1513_1390-151 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210954 | ||||||
chrX:10210956 | C | CT | 26 | a0001c0001t0001g0217a0001c0001t0002g0130a0001c0001t0002g0139others(23): Show | 26 | HG01071.hp1 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1390-1493dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210956 | |||||
chrX:10210956 | C | CTT | 2 | a0001c0001t0013g0077a0001c0003t0016g0086 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1390-1494_1390-149 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210956 | |||||
chrX:10210956 | CT | C | 8 | a0001c0001t0001g0246a0001c0001t0002g0082a0001c0001t0002g0161others(5): Show | 8 | HG00323.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1493delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210956 | |||||
chrX:10210974 | T | TA | 1 | a0001c0001t0004g0069 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1390-1490dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10210974 | |||||
chrX:10210990 | G | A | 1 | a0001c0001t0005g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1390-1477G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10210990 | ||||||
chrX:10211051 | A | AG | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1414dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211051 | |||||
chrX:10211071 | G | GA | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1396_1390-139 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211071 | ||||||
chrX:10211077 | C | G | 12 | a0001c0001t0004g0051a0001c0001t0004g0069a0001c0001t0004g0148others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-1390C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211077 | ||||||
chrX:10211107 | A | T | 8 | a0001c0001t0002g0066a0001c0001t0002g0146a0001c0001t0006g0063others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1360A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211107 | ||||||
chrX:10211136 | C | T | 1 | a0001c0002t0004g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1390-1331C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211136 | ||||||
chrX:10211173 | T | TA | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1292dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211173 | |||||
chrX:10211227 | C | CT | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1239dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211227 | |||||
chrX:10211237 | G | C | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1230G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211237 | ||||||
chrX:10211238 | C | A | 1 | a0001c0001t0002g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1390-1229C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211238 | ||||||
chrX:10211265 | C | CA | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1390-1179dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | |||||
chrX:10211265 | C | CAA | 79 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(76): Show | 79 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1390-1180_1390-117 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | |||||
chrX:10211265 | C | CAAA | 8 | a0001c0001t0001g0016a0001c0001t0003g0153a0001c0001t0003g0174others(5): Show | 8 | HG01243.hp1 HG03098.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1181_1390-117 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | |||||
chrX:10211265 | CAA | C | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1390-1180_1390-117 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | |||||
chrX:10211265 | CAAA | C | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1390-1181_1390-117 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | |||||
chrX:10211265 | CAAAAA | C | 1 | a0001c0001t0008g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1390-1183_1390-117 others(9): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211265 | |||||
chrX:10211280 | A | AG | 2 | a0001c0001t0040g0156a0001c0002t0039g0155 | 2 | HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1390-1187_1390-118 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211280 | ||||||
chrX:10211280 | A | G | 16 | a0001c0001t0002g0130a0001c0001t0004g0051a0001c0001t0004g0148others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1390-1187A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211280 | ||||||
chrX:10211489 | T | TC | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-976dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211489 | |||||
chrX:10211505 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1390-962G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211505 | ||||||
chrX:10211676 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1390-791G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211676 | ||||||
chrX:10211744 | T | A | 3 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1390-723T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211744 | ||||||
chrX:10211791 | G | A | 1 | a0001c0001t0030g0255 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1390-676G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211791 | ||||||
chrX:10211884 | A | G | 4 | a0001c0002t0002g0041a0001c0002t0002g0052a0001c0002t0002g0053others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-583A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211884 | ||||||
chrX:10211943 | T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 179 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(176): Show |
intron_variant | MODIFIER | c.1390-524T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10211943 | ||||||
chrX:10211963 | AG | A | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-501delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10211963 | |||||
chrX:10212015 | C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0172a0001c0001t0001g0199others(1): Show | 4 | HG00738.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-452C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212015 | ||||||
chrX:10212139 | T | TC | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-327dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10212139 | |||||
chrX:10212259 | C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0126others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1390-208C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212259 | ||||||
chrX:10212309 | TC | T | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-155delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10212309 | |||||
chrX:10212377 | GC | G | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1390-87delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 10212377 | |||||
chrX:10212409 | C | T | 44 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0113others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1390-58C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212409 | ||||||
chrX:10212463 | C | T | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.1390-4C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 9/12 | chrX | 10212463 | ||||||
chrX:10212778 | A | G | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1576+125A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212778 | ||||||
chrX:10212809 | C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0023others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1576+156C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212809 | ||||||
chrX:10212837 | G | GCA | 124 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1576+185_1576+186d others(4): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACA | 2 | a0001c0001t0001g0201a0001c0001t0003g0207 | 2 | NA18959.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1576+186_1576+187i others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(1): Show |
4 | a0001c0001t0006g0062a0001c0001t0008g0037a0001c0001t0008g0055others(1): Show | 4 | HG02293.hp2 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(3): Show |
1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1576+186_1576+187i others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(9): Show |
3 | a0001c0001t0003g0224a0001c0001t0005g0079a0001c0001t0009g0078 | 3 | HG01243.hp1 NA18973.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1576+186_1576+187i others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(11): Show |
8 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0002g0146others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(13): Show |
46 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0023others(43): Show | 46 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(15): Show |
7 | a0001c0001t0002g0066a0001c0001t0003g0140a0001c0001t0003g0194others(4): Show | 7 | HG00280.hp1 HG02809.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(17): Show |
9 | a0001c0001t0002g0193a0001c0001t0005g0060a0001c0001t0005g0143others(6): Show | 9 | HG01255.hp1 HG01261.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576+186_1576+187i others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(21): Show |
1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1576+186_1576+187i others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212837 | G | GCACACAC others(25): Show |
1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1576+186_1576+187i others(34): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212837 | |||||
chrX:10212840 | G | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1576+187G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212840 | ||||||
chrX:10212852 | C | G | 1 | a0001c0002t0004g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1576+199C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212852 | ||||||
chrX:10212859 | A | ACACACAC others(16): Show |
1 | a0001c0001t0003g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1576+206_1576+207i others(25): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212859 | ||||||
chrX:10212955 | C | T | 5 | a0001c0001t0002g0066a0001c0001t0005g0060a0001c0001t0005g0143others(2): Show | 5 | HG02809.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576+302C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10212955 | ||||||
chrX:10212989 | T | TA | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1576+339dupA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10212989 | |||||
chrX:10213051 | AT | A | 55 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0111others(52): Show | 55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1576+402delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10213051 | |||||
chrX:10213077 | T | C | 1 | a0001c0001t0034g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1576+424T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213077 | ||||||
chrX:10213174 | G | A | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1577-507G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213174 | ||||||
chrX:10213239 | G | C | 1 | a0001c0001t0003g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1577-442G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213239 | ||||||
chrX:10213253 | G | GCTT | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1577-425_1577-423d others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10213253 | |||||
chrX:10213295 | C | A | 57 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0111others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1577-386C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213295 | ||||||
chrX:10213295 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1577-386C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213295 | ||||||
chrX:10213477 | T | G | 3 | a0001c0001t0010g0168a0001c0001t0010g0169a0001c0002t0039g0155 | 3 | HG01255.hp1 HG01261.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1577-204T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213477 | ||||||
chrX:10213486 | AG | A | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1577-193delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10213486 | |||||
chrX:10213503 | GC | G | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1577-176delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 10213503 | |||||
chrX:10213641 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1577-40G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213641 | ||||||
chrX:10213675 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.1577-6T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 10/12 | chrX | 10213675 | ||||||
chrX:10214209 | G | T | 1 | a0001c0001t0004g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1975+130G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214209 | ||||||
chrX:10214304 | G | A | 4 | a0001c0001t0009g0078a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+225G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214304 | ||||||
chrX:10214359 | T | TG | 1 | a0003c0006t0027g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1975+283dupG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10214359 | |||||
chrX:10214362 | G | C | 3 | a0001c0002t0002g0052a0001c0002t0002g0053a0001c0002t0002g0074 | 3 | HG01884.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1975+283G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214362 | ||||||
chrX:10214373 | T | C | 10 | a0001c0001t0004g0051a0001c0002t0002g0039a0001c0002t0002g0040others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975+294T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214373 | ||||||
chrX:10214520 | A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(143): Show | 147 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1975+441A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214520 | ||||||
chrX:10214531 | G | A | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1975+452G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214531 | ||||||
chrX:10214581 | T | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 106 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.1975+502T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214581 | ||||||
chrX:10214711 | A | G | 1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1975+632A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214711 | ||||||
chrX:10214772 | T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 160 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1975+693T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214772 | ||||||
chrX:10214778 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1975+699C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10214778 | ||||||
chrX:10215062 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1975+983C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215062 | ||||||
chrX:10215150 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1975+1071C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215150 | ||||||
chrX:10215399 | C | T | 4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0036g0017others(1): Show | 4 | HG03669.hp2 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+1320C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215399 | ||||||
chrX:10215471 | CTTA | C | 1 | a0001c0001t0004g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1975+1397_1975+139 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10215471 | |||||
chrX:10215485 | T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(210): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1975+1406T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215485 | ||||||
chrX:10215486 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1975+1407G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215486 | ||||||
chrX:10215520 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1975+1441A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215520 | ||||||
chrX:10215600 | TA | T | 1 | a0001c0001t0015g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1975+1526delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10215600 | |||||
chrX:10215625 | C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1975+1546C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10215625 | ||||||
chrX:10216086 | A | G | 2 | a0001c0001t0009g0061a0001c0002t0013g0035 | 2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1975+2007A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216086 | ||||||
chrX:10216186 | G | A | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1975+2107G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216186 | ||||||
chrX:10216449 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1975+2370C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216449 | ||||||
chrX:10216455 | T | G | 4 | a0001c0001t0010g0168a0001c0001t0010g0169a0001c0001t0034g0073others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2376T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216455 | ||||||
chrX:10216744 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1975+2665A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216744 | ||||||
chrX:10216767 | T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(82): Show | 86 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1975+2688T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216767 | ||||||
chrX:10216878 | G | GGTGT | 3 | a0001c0001t0005g0079a0001c0003t0016g0086a0001c0003t0016g0087 | 3 | HG03516.hp2 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1975+2799_1975+280 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216878 | ||||||
chrX:10216879 | A | ATGTG | 12 | a0001c0001t0001g0227a0001c0001t0001g0233a0001c0001t0001g0251others(9): Show | 12 | HG02129.hp1 HG03490.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1975+2816_1975+281 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | |||||
chrX:10216879 | A | ATGTGTG | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0180 | 3 | HG00597.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1975+2814_1975+281 others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | |||||
chrX:10216879 | A | ATGTGTGT others(1): Show |
10 | a0001c0001t0002g0135a0001c0001t0007g0107a0001c0001t0008g0095others(7): Show | 10 | HG01255.hp1 HG01261.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975+2812_1975+281 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | |||||
chrX:10216879 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1975+2810_1975+281 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216879 | |||||
chrX:10216879 | A | G | 6 | a0001c0001t0002g0066a0001c0001t0005g0060a0001c0001t0005g0079others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1975+2800A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216879 | ||||||
chrX:10216895 | G | GTATATAT others(7): Show |
1 | a0001c0002t0004g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | |||||
chrX:10216895 | G | GTATATAT others(9): Show |
2 | a0001c0002t0004g0048a0001c0002t0004g0049 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1975+2817_1975+281 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | |||||
chrX:10216895 | G | GTATATAT others(25): Show |
1 | a0001c0001t0004g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(36): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | |||||
chrX:10216895 | G | GTATATAT others(27): Show |
1 | a0001c0002t0004g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | |||||
chrX:10216895 | G | GTATATAT others(35): Show |
1 | a0001c0001t0004g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1975+2817_1975+281 others(46): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216895 | |||||
chrX:10216897 | G | A | 11 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0148others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1975+2818G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216897 | ||||||
chrX:10216897 | G | GTATATAT others(3): Show |
1 | a0001c0001t0004g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1975+2831_1975+284 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(7): Show |
1 | a0001c0001t0004g0263 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1975+2827_1975+284 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(9): Show |
1 | a0001c0001t0004g0112 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1975+2825_1975+284 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(13): Show |
1 | a0001c0001t0004g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1975+2821_1975+284 others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(15): Show |
6 | a0001c0001t0004g0028a0001c0001t0004g0088a0001c0001t0004g0092others(3): Show | 6 | HG01516.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975+2819_1975+284 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(17): Show |
6 | a0001c0001t0004g0054a0001c0001t0004g0069a0001c0001t0004g0070others(3): Show | 6 | HG01123.hp1 HG01256.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(19): Show |
4 | a0001c0001t0004g0190a0001c0001t0019g0261a0001c0002t0002g0074others(1): Show | 4 | HG00323.hp2 HG01192.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(21): Show |
4 | a0001c0001t0004g0158a0001c0002t0002g0039a0001c0002t0002g0040others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(32): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(23): Show |
5 | a0001c0001t0004g0138a0001c0001t0004g0258a0001c0002t0002g0052others(2): Show | 5 | HG01358.hp1 HG01884.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(34): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(27): Show |
2 | a0001c0002t0004g0050a0001c0002t0037g0032 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(33): Show |
1 | a0001c0001t0004g0177 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(44): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTATATAT others(37): Show |
1 | a0001c0002t0004g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(48): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTATAT others(19): Show |
1 | a0001c0002t0004g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTATAT others(45): Show |
1 | a0001c0002t0018g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(56): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTAT others(1): Show |
2 | a0001c0001t0004g0137a0001c0001t0013g0077 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTAT others(3): Show |
13 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0024others(10): Show | 13 | HG01257.hp2 HG01258.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTAT others(5): Show |
64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(61): Show | 65 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTAT others(7): Show |
38 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0232others(35): Show | 38 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTAT others(9): Show |
1 | a0001c0001t0001g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0008g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(7): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0008g0055others(1): Show | 4 | HG02083.hp1 HG02293.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(9): Show |
3 | a0001c0001t0002g0066a0001c0001t0005g0060a0001c0001t0005g0143 | 3 | HG02809.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(3): Show |
3 | a0001c0001t0006g0062a0001c0001t0034g0073a0001c0008t0002g0099 | 3 | HG02630.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(5): Show |
9 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(7): Show |
17 | a0001c0001t0001g0230a0001c0001t0002g0019a0001c0001t0002g0021others(14): Show | 17 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(9): Show |
3 | a0001c0001t0002g0010a0001c0001t0002g0022a0001c0001t0002g0119 | 3 | NA18997.hp2 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(11): Show |
7 | a0001c0001t0001g0091a0001c0001t0003g0071a0001c0001t0003g0104others(4): Show | 7 | HG00639.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(22): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(5): Show |
2 | a0001c0001t0002g0097a0001c0001t0029g0098 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(7): Show |
3 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0152 | 3 | HG01891.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0028g0090 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1975+2819_1975+282 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216897 | G | GTGTGTGT others(15): Show |
3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0145 | 3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1975+2819_1975+282 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216897 | |||||
chrX:10216899 | A | G | 11 | a0001c0001t0001g0175a0001c0001t0003g0020a0001c0001t0006g0063others(8): Show | 11 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1975+2820A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216899 | ||||||
chrX:10216901 | A | G | 4 | a0001c0001t0001g0175a0001c0001t0003g0020a0001c0002t0013g0035others(1): Show | 4 | HG03486.hp1 NA18942.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2822A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216901 | ||||||
chrX:10216916 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0012g0136others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975+2838_1975+283 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216916 | |||||
chrX:10216916 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1975+2838_1975+283 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216916 | |||||
chrX:10216918 | T | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0043others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1975+2839T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216918 | ||||||
chrX:10216918 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0197a0001c0001t0002g0010others(1): Show | 4 | HG00621.hp1 NA19079.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975+2845_1975+285 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TACACACA others(3): Show |
165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.1975+2843_1975+285 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TACACACA others(5): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0027others(10): Show | 14 | HG00280.hp1 HG01346.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1975+2841_1975+285 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TACACACA others(7): Show |
1 | a0001c0001t0008g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1975+2852_1975+285 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATACACA others(5): Show |
1 | a0001c0001t0001g0175 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATACACA others(7): Show |
1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(15): Show |
1 | a0001c0001t0036g0017 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(9): Show |
2 | a0001c0001t0009g0061a0001c0001t0009g0078 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(15): Show |
6 | a0001c0001t0001g0227a0001c0001t0001g0233a0001c0001t0003g0213others(3): Show | 6 | HG02293.hp1 HG03490.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(26): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(17): Show |
4 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0003t0016g0086others(1): Show | 4 | HG03516.hp2 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(17): Show |
3 | a0001c0001t0002g0164a0001c0001t0003g0160a0001c0001t0020g0173 | 3 | NA18948.hp1 NA18960.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(28): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(19): Show |
1 | a0001c0001t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(30): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(21): Show |
1 | a0001c0001t0025g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(32): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(25): Show |
2 | a0001c0001t0006g0063a0001c0001t0032g0067 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(36): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(27): Show |
1 | a0001c0001t0006g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(38): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(29): Show |
1 | a0001c0001t0006g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(40): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(25): Show |
1 | a0001c0001t0004g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(36): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(33): Show |
1 | a0001c0001t0006g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(44): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(29): Show |
2 | a0001c0001t0004g0133a0001c0001t0017g0057 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1975+2840_1975+284 others(40): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(33): Show |
1 | a0001c0001t0004g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(44): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(35): Show |
1 | a0001c0001t0004g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(46): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216918 | T | TATATATA others(37): Show |
1 | a0001c0002t0004g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1975+2840_1975+284 others(48): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10216918 | |||||
chrX:10216989 | T | C | 1 | a0001c0001t0013g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1975+2910T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10216989 | ||||||
chrX:10217026 | C | G | 1 | a0001c0001t0034g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1975+2947C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217026 | ||||||
chrX:10217105 | TA | T | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1975+3033delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217105 | |||||
chrX:10217112 | A | T | 1 | a0001c0001t0008g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1975+3033A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217112 | ||||||
chrX:10217267 | A | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1975+3188A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217267 | ||||||
chrX:10217271 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1975+3192T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217271 | ||||||
chrX:10217382 | G | A | 1 | a0001c0001t0004g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1976-3279G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217382 | ||||||
chrX:10217481 | CT | C | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1976-3177delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217481 | |||||
chrX:10217508 | G | A | 1 | a0001c0001t0028g0090 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1976-3153G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217508 | ||||||
chrX:10217526 | T | TCC | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1976-3133_1976-313 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217526 | |||||
chrX:10217563 | GC | G | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1976-3096delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217563 | |||||
chrX:10217650 | T | A | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1976-3011T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217650 | ||||||
chrX:10217746 | CA | C | 4 | a0001c0001t0008g0037a0001c0001t0008g0055a0001c0001t0008g0056others(1): Show | 4 | HG02109.hp1 HG02293.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1976-2914delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217746 | ||||||
chrX:10217747 | A | AT | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1976-2899dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217747 | |||||
chrX:10217747 | A | ATT | 3 | a0001c0001t0001g0013a0001c0001t0001g0236a0001c0001t0034g0073 | 3 | HG01070.hp1 NA18906.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1976-2900_1976-289 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217747 | |||||
chrX:10217812 | G | T | 4 | a0001c0001t0009g0061a0001c0001t0009g0078a0001c0001t0013g0077others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-2849G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217812 | ||||||
chrX:10217813 | G | A | 2 | a0001c0001t0004g0070a0001c0001t0004g0112 | 2 | HG00099.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1976-2848G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217813 | ||||||
chrX:10217817 | AC | A | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1976-2840delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217817 | |||||
chrX:10217864 | TC | T | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1976-2794delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chrX | 10217864 | |||||
chrX:10217901 | CG | C | 1 | a0001c0001t0002g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1976-2759delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217901 | ||||||
chrX:10217963 | G | A | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-2698G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217963 | ||||||
chrX:10217986 | G | A | 1 | a0001c0001t0036g0017 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1976-2675G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217986 | ||||||
chrX:10217989 | C | T | 1 | a0001c0001t0009g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1976-2672C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10217989 | ||||||
chrX:10218070 | G | C | 4 | a0001c0001t0008g0037a0001c0001t0008g0055a0001c0001t0008g0056others(1): Show | 4 | HG02109.hp1 HG02293.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1976-2591G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218070 | ||||||
chrX:10218120 | A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0235 | 2 | HG02027.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1976-2541A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218120 | ||||||
chrX:10218321 | T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(223): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1976-2340T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218321 | ||||||
chrX:10218588 | T | A | 2 | a0001c0001t0036g0017a0001c0002t0015g0030 | 2 | HG03669.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1976-2073T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10218588 | ||||||
chrX:10219080 | T | G | 9 | a0001c0001t0004g0028a0001c0001t0004g0070a0001c0001t0004g0088others(6): Show | 9 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1976-1581T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219080 | ||||||
chrX:10219327 | G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1976-1334G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219327 | ||||||
chrX:10219445 | G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 159 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1976-1216G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219445 | ||||||
chrX:10219463 | G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0215 | 2 | NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1976-1198G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219463 | ||||||
chrX:10219916 | A | G | 1 | a0001c0001t0006g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1976-745A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10219916 | ||||||
chrX:10220044 | G | T | 8 | a0001c0001t0005g0060a0001c0001t0005g0079a0001c0001t0005g0143others(5): Show | 8 | HG02809.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1976-617G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220044 | ||||||
chrX:10220335 | A | T | 1 | a0001c0001t0003g0176 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1976-326A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220335 | ||||||
chrX:10220352 | G | A | 2 | a0001c0001t0004g0092a0001c0001t0004g0093 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1976-309G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220352 | ||||||
chrX:10220527 | T | C | 2 | a0001c0001t0004g0054a0001c0001t0004g0069 | 2 | HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1976-134T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 11/12 | chrX | 10220527 | ||||||
chrX:10221210 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2192+333A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221210 | ||||||
chrX:10221212 | A | G | 7 | a0001c0001t0008g0037a0001c0001t0008g0055a0001c0001t0008g0056others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2192+335A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221212 | ||||||
chrX:10221547 | G | T | 1 | a0001c0002t0026g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2192+670G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221547 | ||||||
chrX:10221781 | G | A | 1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2192+904G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221781 | ||||||
chrX:10221798 | G | A | 2 | a0001c0002t0004g0048a0001c0002t0004g0049 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2192+921G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10221798 | ||||||
chrX:10222101 | G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(150): Show | 154 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.2192+1224G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10222101 | ||||||
chrX:10222128 | C | T | 3 | a0001c0001t0007g0141a0001c0001t0007g0142a0001c0001t0007g0145 | 3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2192+1251C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10222128 | ||||||
chrX:10222628 | G | A | 71 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(68): Show | 71 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2192+1751G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10222628 | ||||||
chrX:10223280 | C | A | 1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2192+2403C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223280 | ||||||
chrX:10223284 | A | T | 69 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2192+2407A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223284 | ||||||
chrX:10223295 | G | A | 2 | a0001c0002t0004g0048a0001c0002t0004g0049 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2192+2418G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223295 | ||||||
chrX:10223341 | C | T | 1 | a0001c0001t0029g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2192+2464C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223341 | ||||||
chrX:10223606 | G | A | 1 | a0001c0001t0003g0207 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2192+2729G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223606 | ||||||
chrX:10223706 | C | T | 2 | a0001c0001t0003g0174a0002c0004t0003g0196 | 2 | NA18974.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2192+2829C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223706 | ||||||
chrX:10223815 | A | G | 1 | a0001c0001t0009g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2192+2938A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223815 | ||||||
chrX:10223874 | T | C | 3 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0022 | 3 | NA19079.hp1 NA19080.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2192+2997T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10223874 | ||||||
chrX:10224191 | T | TAA | 8 | a0001c0001t0003g0160a0001c0001t0003g0174a0001c0001t0003g0191others(5): Show | 8 | HG01934.hp1 NA18948.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2192+3317_2192+331 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224191 | |||||
chrX:10224248 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2192+3371A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224248 | ||||||
chrX:10224275 | A | G | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3398A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224275 | ||||||
chrX:10224293 | C | CGT | 34 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0026others(31): Show | 34 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.2192+3455_2192+345 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGT | 7 | a0001c0001t0001g0236a0001c0001t0002g0139a0001c0001t0031g0241others(4): Show | 7 | HG01346.hp2 HG02615.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2192+3453_2192+345 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGTGT | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(56): Show | 59 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2192+3451_2192+345 others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGTGTG others(1): Show |
25 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0024others(22): Show | 26 | HG00597.hp1 HG00735.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.2192+3449_2192+345 others(12): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGTGTG others(3): Show |
7 | a0001c0001t0001g0219a0001c0001t0002g0076a0001c0001t0002g0082others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.2192+3447_2192+345 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGTGTG others(5): Show |
5 | a0001c0001t0002g0096a0001c0001t0002g0135a0001c0001t0002g0152others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2192+3445_2192+345 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGTGTG others(7): Show |
3 | a0001c0001t0002g0094a0001c0001t0002g0102a0001c0005t0002g0100 | 3 | HG02258.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2192+3443_2192+345 others(18): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0002g0097a0001c0007t0012g0101 | 2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2192+3441_2192+345 others(20): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | CGT | C | 58 | a0001c0001t0001g0016a0001c0001t0001g0091a0001c0001t0001g0197others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.2192+3455_2192+345 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | CGTGT | C | 7 | a0001c0001t0003g0160a0001c0001t0003g0222a0001c0001t0005g0060others(4): Show | 7 | HG01074.hp1 HG02809.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2192+3453_2192+345 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | CGTGTGT | C | 4 | a0001c0001t0009g0061a0001c0001t0013g0077a0001c0001t0032g0067others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3451_2192+345 others(10): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224293 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0015g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2192+3447_2192+345 others(14): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224293 | |||||
chrX:10224318 | G | A | 1 | a0001c0008t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2192+3441G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224318 | ||||||
chrX:10224319 | TGTGTGTG others(13): Show |
T | 1 | a0001c0008t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2192+3455_2192+347 others(24): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224319 | |||||
chrX:10224320 | G | A | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3443G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224320 | ||||||
chrX:10224325 | T | A | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3448T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224325 | ||||||
chrX:10224327 | TGTGTGTA others(5): Show |
T | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+3457_2192+346 others(16): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224327 | |||||
chrX:10224406 | A | G | 69 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2192+3529A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224406 | ||||||
chrX:10224474 | TA | T | 51 | a0001c0001t0001g0016a0001c0001t0001g0197a0001c0001t0001g0215others(48): Show | 51 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2192+3609delA | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10224474 | |||||
chrX:10224656 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2192+3779G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10224656 | ||||||
chrX:10225047 | G | A | 1 | a0001c0002t0026g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2192+4170G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225047 | ||||||
chrX:10225319 | G | C | 1 | a0001c0001t0011g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2192+4442G>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225319 | ||||||
chrX:10225390 | T | C | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2192+4513T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225390 | ||||||
chrX:10225580 | G | T | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2192+4703G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225580 | ||||||
chrX:10225581 | A | T | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2192+4704A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225581 | ||||||
chrX:10225840 | T | C | 67 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(64): Show | 67 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2192+4963T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225840 | ||||||
chrX:10225879 | T | A | 1 | a0001c0001t0029g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2192+5002T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10225879 | ||||||
chrX:10226003 | G | A | 59 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(56): Show | 59 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2192+5126G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226003 | ||||||
chrX:10226008 | A | G | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192+5131A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226008 | ||||||
chrX:10226245 | AACC | A | 58 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(55): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.2192+5374_2192+537 others(7): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10226245 | |||||
chrX:10226317 | GC | G | 1 | a0001c0001t0034g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2192+5441delC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226317 | ||||||
chrX:10226360 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2192+5483C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10226360 | ||||||
chrX:10226803 | AATAG | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0120 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2192+5930_2192+593 others(8): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10226803 | |||||
chrX:10227035 | G | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(150): Show | 154 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.2192+6158G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227035 | ||||||
chrX:10227235 | A | G | 1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2193-6259A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227235 | ||||||
chrX:10227247 | C | T | 1 | a0001c0001t0003g0222 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2193-6247C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227247 | ||||||
chrX:10227253 | C | G | 1 | a0001c0002t0026g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2193-6241C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227253 | ||||||
chrX:10227548 | T | A | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2193-5946T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227548 | ||||||
chrX:10227751 | A | G | 1 | a0001c0002t0009g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2193-5743A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10227751 | ||||||
chrX:10227921 | GT | G | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0148others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2193-5570delT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10227921 | |||||
chrX:10228158 | A | AT | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-5335dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10228158 | |||||
chrX:10228486 | G | T | 2 | a0001c0001t0005g0060a0001c0001t0005g0143 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2193-5008G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228486 | ||||||
chrX:10228498 | A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 146 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2193-4996A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228498 | ||||||
chrX:10228546 | G | T | 1 | a0001c0001t0036g0017 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2193-4948G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228546 | ||||||
chrX:10228572 | A | C | 1 | a0001c0001t0001g0254 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2193-4922A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228572 | ||||||
chrX:10228607 | C | G | 72 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(69): Show | 72 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2193-4887C>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10228607 | ||||||
chrX:10229021 | T | G | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-4473T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229021 | ||||||
chrX:10229386 | AAT | A | 16 | a0001c0001t0005g0060a0001c0001t0005g0079a0001c0001t0005g0143others(13): Show | 16 | HG02615.hp1 HG02622.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.2193-4091_2193-409 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10229386 | |||||
chrX:10229390 | T | A | 8 | a0001c0001t0006g0062a0001c0001t0006g0063a0001c0001t0006g0064others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2193-4104T>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229390 | ||||||
chrX:10229392 | T | C | 2 | a0001c0001t0029g0098a0001c0001t0034g0073 | 2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2193-4102T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229392 | ||||||
chrX:10229442 | C | T | 60 | a0001c0001t0001g0091a0001c0001t0002g0010a0001c0001t0002g0019others(57): Show | 60 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2193-4052C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229442 | ||||||
chrX:10229544 | G | GTC | 1 | a0001c0001t0001g0236 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2193-3949_2193-394 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10229544 | |||||
chrX:10229545 | T | TC | 12 | a0001c0001t0001g0183a0001c0001t0001g0197a0001c0001t0002g0125others(9): Show | 12 | HG00621.hp1 HG01256.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-3943dupC | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10229545 | |||||
chrX:10229546 | C | CT | 1 | a0002c0004t0003g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2193-3948_2193-394 others(5): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229546 | ||||||
chrX:10229569 | G | A | 8 | a0001c0001t0005g0060a0001c0001t0005g0079a0001c0001t0005g0143others(5): Show | 8 | HG02809.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.2193-3925G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229569 | ||||||
chrX:10229937 | A | G | 1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2193-3557A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10229937 | ||||||
chrX:10230096 | G | T | 2 | a0001c0001t0004g0109a0001c0001t0004g0190 | 2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2193-3398G>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10230096 | ||||||
chrX:10230110 | A | AT | 12 | a0001c0001t0008g0037a0001c0001t0008g0055a0001c0001t0008g0056others(9): Show | 12 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-3379dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10230110 | |||||
chrX:10230348 | A | G | 1 | a0001c0001t0034g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2193-3146A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10230348 | ||||||
chrX:10230647 | C | T | 4 | a0001c0002t0004g0045a0001c0002t0004g0046a0001c0002t0004g0048others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-2847C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10230647 | ||||||
chrX:10231166 | C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0233 | 2 | NA18952.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2193-2328C>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231166 | ||||||
chrX:10231345 | ACC | A | 1 | a0001c0002t0015g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2193-2148_2193-214 others(6): Show |
CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231345 | ||||||
chrX:10231348 | A | AT | 1 | a0001c0001t0035g0231 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2193-2145dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10231348 | |||||
chrX:10231358 | A | G | 12 | a0001c0001t0008g0037a0001c0001t0008g0055a0001c0001t0008g0056others(9): Show | 12 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-2136A>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231358 | ||||||
chrX:10231516 | A | C | 1 | a0001c0001t0002g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2193-1978A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231516 | ||||||
chrX:10231544 | T | G | 12 | a0001c0001t0008g0037a0001c0001t0008g0055a0001c0001t0008g0056others(9): Show | 12 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2193-1950T>G | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10231544 | ||||||
chrX:10232115 | AG | A | 1 | a0001c0001t0035g0231 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2193-1375delG | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10232115 | |||||
chrX:10232332 | C | CT | 1 | a0001c0001t0035g0231 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2193-1161dupT | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 10232332 | |||||
chrX:10232388 | G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.2193-1106G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232388 | ||||||
chrX:10232389 | T | C | 2 | a0001c0001t0013g0077a0001c0002t0013g0035 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2193-1105T>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232389 | ||||||
chrX:10232503 | C | A | 1 | a0001c0002t0013g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2193-991C>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232503 | ||||||
chrX:10232586 | A | C | 4 | a0001c0001t0010g0059a0001c0001t0010g0168a0001c0001t0010g0169others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-908A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232586 | ||||||
chrX:10232709 | A | C | 1 | a0001c0002t0004g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2193-785A>C | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232709 | ||||||
chrX:10232873 | G | A | 58 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0021others(55): Show | 58 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.2193-621G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10232873 | ||||||
chrX:10233127 | G | A | 59 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0021others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2193-367G>A | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10233127 | ||||||
chrX:10233274 | A | T | 1 | a0001c0002t0026g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2193-220A>T | CLCN4 | ENSG00000073464.13 | transcript | ENST00000380833.9 | protein_coding | 12/12 | chrX | 10233274 |